Explore diverse job opportunities in Waterford, a city blending rich history with modern industry. Waterford's job market presents roles across various sectors, from 128 Jobs in Waterford
Analytical Researcher
Waterford, Munster
Teva Pharmaceuticals
Posted today
Job Viewed
Job Description
Analytical Researcher
Date: Sep 4, 2025
Location:
Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 63744
**Who We Are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The Opportunity**
We would like to invite applications for the role of an permanent Analytical Researcher position at our Waterford Site.
This provides an exciting opportunity to work within the dynamic and ever changing environment of R&D as part of the product development team for a global leader in the pharmaceutical sector. Teva Respiratory R&D is seeking a highly innovative, data-driven and self-motivated individual with strength in analytical pharmaceutical product development. If you're dedicated, energetic and detail-oriented, this could be the perfect role for you!
Key Responsibilities:
+ Heavily involved, or occasion leading, scientific/technical investigations and develop approaches to solve wide ranging, difficult and complex problems.
+ Working closely with product development teams and/or processes, characterisation, investigations and root cause analyses.
+ Compilation and review of detailed technical documents.
+ Ensuring that work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, regulatory, H&S and environmental requirements.
+ Working cross-functionally with significant communication channels between departments such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
+ Contributing to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies.
+ Delivering excellent customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines.
**Your Experience And Qualifications**
Do You Have:
+ Career experience within a Pharmaceutical laboratory setting.
+ Experience working to current Good Manufacturing Practice and/or Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines.
+ Knowledge of global regulatory and compliance requirements.
+ Excellent planning and organising skills & adaptable to changing priorities.
Are You:
+ Bringing a breadth of data analysis skills.
+ A confident communicator both verbally and in writing.
+ Valuing colleague collaboration and team building.
If so, we'd value hearing from you!
**Reports To**
Jamie Fitzpatrick
Senior Supervisor, Analytical R&D
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
Date: Sep 4, 2025
Location:
Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 63744
**Who We Are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The Opportunity**
We would like to invite applications for the role of an permanent Analytical Researcher position at our Waterford Site.
This provides an exciting opportunity to work within the dynamic and ever changing environment of R&D as part of the product development team for a global leader in the pharmaceutical sector. Teva Respiratory R&D is seeking a highly innovative, data-driven and self-motivated individual with strength in analytical pharmaceutical product development. If you're dedicated, energetic and detail-oriented, this could be the perfect role for you!
Key Responsibilities:
+ Heavily involved, or occasion leading, scientific/technical investigations and develop approaches to solve wide ranging, difficult and complex problems.
+ Working closely with product development teams and/or processes, characterisation, investigations and root cause analyses.
+ Compilation and review of detailed technical documents.
+ Ensuring that work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, regulatory, H&S and environmental requirements.
+ Working cross-functionally with significant communication channels between departments such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
+ Contributing to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies.
+ Delivering excellent customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines.
**Your Experience And Qualifications**
Do You Have:
+ Career experience within a Pharmaceutical laboratory setting.
+ Experience working to current Good Manufacturing Practice and/or Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines.
+ Knowledge of global regulatory and compliance requirements.
+ Excellent planning and organising skills & adaptable to changing priorities.
Are You:
+ Bringing a breadth of data analysis skills.
+ A confident communicator both verbally and in writing.
+ Valuing colleague collaboration and team building.
If so, we'd value hearing from you!
**Reports To**
Jamie Fitzpatrick
Senior Supervisor, Analytical R&D
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
This advertiser has chosen not to accept applicants from your region.
0
Account Executive ( South East & South West Ireland)
Waterford, Munster
Diageo
Posted today
Job Viewed
Job Description
**Job Description :**
Diageo is the world's leading premium drinks company with an outstanding collection of brands, such as Johnnie Walker, Smirnoff, Baileys, Captain Morgan, Tanqueray and Guinness. Our purpose - Celebrating life, every day, everywhere - has a meaningful role in our company, for our people, our diversity, our brands, in how we perform and how we create shared value.
**Join Us at Diageo's Assessment Centre for Account Executives!**
Are you ready to take your career to the next level with one of the world's leading beverage alcohol companies? Diageo is excited to invite talented and ambitious individuals to our upcoming Assessment Centre for the role of Account Executive for South East Ireland. This is a unique opportunity to showcase your skills through individual and group exercises, connect with industry leaders, and potentially secure a position that offers growth, innovation, and the chance to work with iconic brands.
**Day in the Life** **:**
+ **Strategic Relationship Builder:** Build strong, purposeful relationships and effectively support existing customers. Carry out regular business reviews to identify their needs and goals. Create growth plans and implement solutions to drive sustainable growth.
+ **Dynamic Communicator:** Effectively communicate with customers and internal teams to ensure alignment on goals and strategies. Be adaptable in your communication style to meet the needs of diverse stakeholders.
+ **Commercial Acumen:** Drive the brand distribution strategy to increase the quality and quantity of customer partnerships within your territory.
+ **Data Acumen:** Ensure all data on your territory is accurate and up-to-date, including territory performance, customer contact details, digital savviness, new/closed outlets, etc.
+ **Digital First Mindset:** Embrace and leveragedigital tools always. Engage both internally and externally on key initiatives and evolving trends.
+ **Growth/ Open Mindset:** Bring a growth mindset to all that you do. Embrace challenges, learn continuously, and drive innovation for sustainable success.
+ **Resilience:** Demonstrate resilience in overcoming challenges and persistently pursue long-term goals despite short-term setbacks.
ABOUT YOU
+ Passionate about sales and to grow a career within commercial
+ Driver's license
Celebrating our inclusive and diverse culture is core to Diageo's purpose of "celebrating life every day everywhere". This purpose is, in itself, inclusive in nature, as it values everybody irrespective of background, disability, religion, gender identity, sexuality or ethnicity.
We know that for Diageo to thrive and for us to realize our ambition, we depend on having diverse talent with a range of backgrounds, skills and capabilities in each of the 180 countries in which we operate and to reflect our broad consumer base. We view diversity as one of the key enablers that helps our business to grow and our values, purpose and standards set the conditions for us to respect the unique contribution each person brings.
Flexibility is key to success in our business and many of our staff work flexibly in many different ways, including part-time, compressed hours, flexible location. Please talk to us about what flexibility means to you and don't let anything stop you from applying.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process and to perform essential job functions.
**Worker Type :**
Regular
**Primary Location:**
St James Gate
**Additional Locations :**
**Job Posting Start Date :**
With over 200 brands sold in more than 180 countries, we're the world's leading premium drinks company. Every day, over 30,000 talented people come together at Diageo to create the magic behind our much-loved brands. From iconic names to innovative newcomers - the brands we're building are rooted in culture and local communities. Our ambition is to be one of the best performing, most trusted and most respected consumer products companies in the world.
Our founders, such as Arthur Guinness, John Walker, and Charles Tanqueray, were visionary entrepreneurs whose brilliant minds helped shape the alcohol industry. And through our people, their legacy lives on. Join us, and you'll collaborate with talented people from all corners of the world. Together, you'll innovate and push boundaries, shaping a more inclusive and sustainable future that we can all be proud of.
With diversity at our core, we celebrate our people's unique passions, commitments and specialist skills. Because when varied voices, mindsets, and personalities come together, great ideas are born. In our supportive culture, your voice will be heard and you'll be empowered to be you. Just bring your ambition, curiosity and ideas, and we'll celebrate your work and help you reach your fullest potential.
**DRINKiQ**
What's your DRINKiQ? Take our quiz to understand how alcohol is made and explore the effects of drinking. You can discover everything you need to know at DRINKiQ (
Diageo is the world's leading premium drinks company with an outstanding collection of brands, such as Johnnie Walker, Smirnoff, Baileys, Captain Morgan, Tanqueray and Guinness. Our purpose - Celebrating life, every day, everywhere - has a meaningful role in our company, for our people, our diversity, our brands, in how we perform and how we create shared value.
**Join Us at Diageo's Assessment Centre for Account Executives!**
Are you ready to take your career to the next level with one of the world's leading beverage alcohol companies? Diageo is excited to invite talented and ambitious individuals to our upcoming Assessment Centre for the role of Account Executive for South East Ireland. This is a unique opportunity to showcase your skills through individual and group exercises, connect with industry leaders, and potentially secure a position that offers growth, innovation, and the chance to work with iconic brands.
**Day in the Life** **:**
+ **Strategic Relationship Builder:** Build strong, purposeful relationships and effectively support existing customers. Carry out regular business reviews to identify their needs and goals. Create growth plans and implement solutions to drive sustainable growth.
+ **Dynamic Communicator:** Effectively communicate with customers and internal teams to ensure alignment on goals and strategies. Be adaptable in your communication style to meet the needs of diverse stakeholders.
+ **Commercial Acumen:** Drive the brand distribution strategy to increase the quality and quantity of customer partnerships within your territory.
+ **Data Acumen:** Ensure all data on your territory is accurate and up-to-date, including territory performance, customer contact details, digital savviness, new/closed outlets, etc.
+ **Digital First Mindset:** Embrace and leveragedigital tools always. Engage both internally and externally on key initiatives and evolving trends.
+ **Growth/ Open Mindset:** Bring a growth mindset to all that you do. Embrace challenges, learn continuously, and drive innovation for sustainable success.
+ **Resilience:** Demonstrate resilience in overcoming challenges and persistently pursue long-term goals despite short-term setbacks.
ABOUT YOU
+ Passionate about sales and to grow a career within commercial
+ Driver's license
Celebrating our inclusive and diverse culture is core to Diageo's purpose of "celebrating life every day everywhere". This purpose is, in itself, inclusive in nature, as it values everybody irrespective of background, disability, religion, gender identity, sexuality or ethnicity.
We know that for Diageo to thrive and for us to realize our ambition, we depend on having diverse talent with a range of backgrounds, skills and capabilities in each of the 180 countries in which we operate and to reflect our broad consumer base. We view diversity as one of the key enablers that helps our business to grow and our values, purpose and standards set the conditions for us to respect the unique contribution each person brings.
Flexibility is key to success in our business and many of our staff work flexibly in many different ways, including part-time, compressed hours, flexible location. Please talk to us about what flexibility means to you and don't let anything stop you from applying.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process and to perform essential job functions.
**Worker Type :**
Regular
**Primary Location:**
St James Gate
**Additional Locations :**
**Job Posting Start Date :**
With over 200 brands sold in more than 180 countries, we're the world's leading premium drinks company. Every day, over 30,000 talented people come together at Diageo to create the magic behind our much-loved brands. From iconic names to innovative newcomers - the brands we're building are rooted in culture and local communities. Our ambition is to be one of the best performing, most trusted and most respected consumer products companies in the world.
Our founders, such as Arthur Guinness, John Walker, and Charles Tanqueray, were visionary entrepreneurs whose brilliant minds helped shape the alcohol industry. And through our people, their legacy lives on. Join us, and you'll collaborate with talented people from all corners of the world. Together, you'll innovate and push boundaries, shaping a more inclusive and sustainable future that we can all be proud of.
With diversity at our core, we celebrate our people's unique passions, commitments and specialist skills. Because when varied voices, mindsets, and personalities come together, great ideas are born. In our supportive culture, your voice will be heard and you'll be empowered to be you. Just bring your ambition, curiosity and ideas, and we'll celebrate your work and help you reach your fullest potential.
**DRINKiQ**
What's your DRINKiQ? Take our quiz to understand how alcohol is made and explore the effects of drinking. You can discover everything you need to know at DRINKiQ (
This advertiser has chosen not to accept applicants from your region.
1
Sterility Assurance Specialist
Waterford, Munster
Sanofi Group
Posted today
Job Viewed
Job Description
**Sterility Assurance Specialist**
+ Location: Waterford, Ireland
+ Fixed Term Contract
**About the job**
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
The Sterility Assurance Specialist will be responsible for developing, implementing, and maintaining sterility assurance programs to ensure compliance with Good Manufacturing Practice (GMP) and regulatory requirements. This role will function as the subject matter expert (SME) for aseptic processing, contamination control, and microbiological quality, supporting manufacturing operations, quality systems, and continuous improvement initiatives.
**Main responsibilities:**
+ Develop, maintain, and improve site sterility assurance strategies and contamination control plans.
+ Lead risk assessments for aseptic processes, cleanroom operations, and sterilisation activities.
+ Ensure compliance with relevant guidelines (e.g., EU GMP Annex 1, FDA Guidance for Industry, ISO standards).
+ Provide SME oversight during aseptic processing, media fills, and environmental monitoring trend reviews. Identifying trends or issues and implementing effective action plans.
+ Support deviation investigations, root cause analysis, and CAPA implementation for sterility-related issues.
+ Review and approve protocols and reports for sterilisation validation, cleanroom qualification, and disinfection studies.
+ Review and approve documentation related to aseptic manufacturing, sterilisation, and microbiological controls.
+ Function as point of contact for sterility assurance during internal and external audits and regulatory inspections.
+ Ensure timely identification and communication of sterility-related risks.
+ Establish and monitor KPIs for the sterility assurance program and report on its performance and effectiveness.
+ Drive improvements in aseptic practices, gowning, cleaning, and contamination control procedures.
+ Deliver training and coaching to manufacturing, QC, and QA teams on sterility assurance principles.
+ Monitor emerging regulatory changes and industry best practices to update site procedures accordingly.
**About you**
+ Bachelor's degree (or higher) in Microbiology, Biology, Pharmacy, or related scientific discipline.
+ Extensive experience in sterility assurance, microbiology, or quality assurance within GMP-regulated manufacturing.
+ Experience leading contamination control strategies and aseptic process validations.
+ Demonstrated track record of successful regulatory inspections.
+ Sterilisation validation experience (e.g., autoclave, VHP, gamma irradiation) desirable.
+ Strong knowledge of aseptic manufacturing, microbiology, sterilisation methods, and cleanroom operations.
+ In-depth understanding of quality and technical regulations in a GMP environment.
+ Analytical mindset with ability to interpret complex microbiological data and environmental monitoring trends.
+ Excellent communication and leadership skills to influence cross-functional teams.
+ Strong problem-solving skills and ability to make decisions under pressure.
**Why choose us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career.
+ Our Waterford site is easily accessible from the M9 and offers excellent facilities including a subsidized restaurant and newly refurbished gym.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
+ Location: Waterford, Ireland
+ Fixed Term Contract
**About the job**
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
The Sterility Assurance Specialist will be responsible for developing, implementing, and maintaining sterility assurance programs to ensure compliance with Good Manufacturing Practice (GMP) and regulatory requirements. This role will function as the subject matter expert (SME) for aseptic processing, contamination control, and microbiological quality, supporting manufacturing operations, quality systems, and continuous improvement initiatives.
**Main responsibilities:**
+ Develop, maintain, and improve site sterility assurance strategies and contamination control plans.
+ Lead risk assessments for aseptic processes, cleanroom operations, and sterilisation activities.
+ Ensure compliance with relevant guidelines (e.g., EU GMP Annex 1, FDA Guidance for Industry, ISO standards).
+ Provide SME oversight during aseptic processing, media fills, and environmental monitoring trend reviews. Identifying trends or issues and implementing effective action plans.
+ Support deviation investigations, root cause analysis, and CAPA implementation for sterility-related issues.
+ Review and approve protocols and reports for sterilisation validation, cleanroom qualification, and disinfection studies.
+ Review and approve documentation related to aseptic manufacturing, sterilisation, and microbiological controls.
+ Function as point of contact for sterility assurance during internal and external audits and regulatory inspections.
+ Ensure timely identification and communication of sterility-related risks.
+ Establish and monitor KPIs for the sterility assurance program and report on its performance and effectiveness.
+ Drive improvements in aseptic practices, gowning, cleaning, and contamination control procedures.
+ Deliver training and coaching to manufacturing, QC, and QA teams on sterility assurance principles.
+ Monitor emerging regulatory changes and industry best practices to update site procedures accordingly.
**About you**
+ Bachelor's degree (or higher) in Microbiology, Biology, Pharmacy, or related scientific discipline.
+ Extensive experience in sterility assurance, microbiology, or quality assurance within GMP-regulated manufacturing.
+ Experience leading contamination control strategies and aseptic process validations.
+ Demonstrated track record of successful regulatory inspections.
+ Sterilisation validation experience (e.g., autoclave, VHP, gamma irradiation) desirable.
+ Strong knowledge of aseptic manufacturing, microbiology, sterilisation methods, and cleanroom operations.
+ In-depth understanding of quality and technical regulations in a GMP environment.
+ Analytical mindset with ability to interpret complex microbiological data and environmental monitoring trends.
+ Excellent communication and leadership skills to influence cross-functional teams.
+ Strong problem-solving skills and ability to make decisions under pressure.
**Why choose us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career.
+ Our Waterford site is easily accessible from the M9 and offers excellent facilities including a subsidized restaurant and newly refurbished gym.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
This advertiser has chosen not to accept applicants from your region.
2
Automation Shift Engineer
Waterford, Munster
Sanofi Group
Posted today
Job Viewed
Job Description
**Automation Engineer**
+ _Grade: L2_
+ _Hiring Manager: Eoin Galvin_
+ _Location Waterford_
+ _Please note 24/7 shift pattern applies for this role_
+ _Full-Time_
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
**Main responsibilities:**
+ Work with the Automation Team to provide Automation support for operations and project implementation.
+ Provide technical support & guidance to Process, Maintenance & Facilities Engineers.
+ Act as the Automation support contact within the Mabs manufacturing area in a shift capacity role.
+ Identify, evaluate & implement opportunities for continuous improvement of the PLC / SCADA Automation Systems & applications.
+ To provide high level Automation support to operations to ensure our automation systems are kept in a compliant manner.
+ Excellent technical knowledge with good operational and/or project engineering experience i.e. all phases of the GAMP life cycle validation phases.
+ Support to the shift Automation Technicians & Engineers.
+ Be responsible for and involved in troubleshooting & maintenance of all production processes and equipment.
+ Work closely with the Process Engineers on Investigations and delivering projects and Continuous Improvements to reduce / eliminate technical issues in the area.
+ Support initiatives / workshops FMEAs as required.
+ Experience of Packaging and/or sterile vial filling an advantage but not essential.
**About you:**
To excel in this role you will need to have:
**Essential requirements:**
+ 3-5 years' experience in a pharmaceutical control systems operational and/or project engineering role.
+ - Experience of PLC systems Siemens Elau an advantage - Experience of SCADA systems Ifix / Wonderware Utility MS and EMS systems.
+ Must have good knowledge of Manufacturing equipment & processes .
+ Strong Diagnostic & faulting abilities.
+ Good Knowledge of PLC / SCADA & Vision systems.
+ Good Knowledge of Electrical systems, Drives Units & associated Schematics.
+ Support to the shift Automation Technicians & Engineers.
+ Responsible for and involved in troubleshooting & maintenance of all production processes and equipment. Working closely with the Process Engineers on Investigations and delivering projects and Continuous Improvements to reduce / eliminate technical issues in the area.
+ Support initiatives / workshops FMEAs as required.
+ Must have good written and verbal communication skills as well as the ability to accurately document work performed.
+ Must be able to organize and prioritize tasks; must be detail orientated and self-motivated.
+ Must be able to work independently on own projects while working concurrently with all departments and levels of employees.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
+ _Grade: L2_
+ _Hiring Manager: Eoin Galvin_
+ _Location Waterford_
+ _Please note 24/7 shift pattern applies for this role_
+ _Full-Time_
**About Waterford**
For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.
**Main responsibilities:**
+ Work with the Automation Team to provide Automation support for operations and project implementation.
+ Provide technical support & guidance to Process, Maintenance & Facilities Engineers.
+ Act as the Automation support contact within the Mabs manufacturing area in a shift capacity role.
+ Identify, evaluate & implement opportunities for continuous improvement of the PLC / SCADA Automation Systems & applications.
+ To provide high level Automation support to operations to ensure our automation systems are kept in a compliant manner.
+ Excellent technical knowledge with good operational and/or project engineering experience i.e. all phases of the GAMP life cycle validation phases.
+ Support to the shift Automation Technicians & Engineers.
+ Be responsible for and involved in troubleshooting & maintenance of all production processes and equipment.
+ Work closely with the Process Engineers on Investigations and delivering projects and Continuous Improvements to reduce / eliminate technical issues in the area.
+ Support initiatives / workshops FMEAs as required.
+ Experience of Packaging and/or sterile vial filling an advantage but not essential.
**About you:**
To excel in this role you will need to have:
**Essential requirements:**
+ 3-5 years' experience in a pharmaceutical control systems operational and/or project engineering role.
+ - Experience of PLC systems Siemens Elau an advantage - Experience of SCADA systems Ifix / Wonderware Utility MS and EMS systems.
+ Must have good knowledge of Manufacturing equipment & processes .
+ Strong Diagnostic & faulting abilities.
+ Good Knowledge of PLC / SCADA & Vision systems.
+ Good Knowledge of Electrical systems, Drives Units & associated Schematics.
+ Support to the shift Automation Technicians & Engineers.
+ Responsible for and involved in troubleshooting & maintenance of all production processes and equipment. Working closely with the Process Engineers on Investigations and delivering projects and Continuous Improvements to reduce / eliminate technical issues in the area.
+ Support initiatives / workshops FMEAs as required.
+ Must have good written and verbal communication skills as well as the ability to accurately document work performed.
+ Must be able to organize and prioritize tasks; must be detail orientated and self-motivated.
+ Must be able to work independently on own projects while working concurrently with all departments and levels of employees.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
This advertiser has chosen not to accept applicants from your region.
3
Key Account Manager
Waterford, Munster
IQVIA
Posted today
Job Viewed
Job Description
**Job Title:** Hospital Key Account Manager - Rheumatology
**Location:** Munster & Leinster, Republic of Ireland
**Position Type:** Field-based
An experienced Secondary Care Specialist is sought to join an established pharmaceutical sales team in the field of rheumatology. This strategic and promotional role focuses on driving product differentiation and uptake across key hospitals and clinical centres in Munster and Leinster.
The role involves leading product promotion to secondary care healthcare professionals, delivering professional presentations, and providing specialist medical education. The successful candidate will ensure that relevant decision-makers understand the clinical benefits of the products to support formulary access and funding.
A key aspect of the role is engaging and developing regional and national opinion leaders to build clinical experience and support therapy area education and access. The candidate will proactively communicate with customers through compliant channels including face-to-face visits, virtual meetings, phone calls, and emails. They will also collaborate with internal stakeholders to implement creative customer engagement initiatives aligned with business plans and strategic investments.
This position requires a high level of collaboration with the national sales and marketing teams and embraces the core values of the organization to contribute to a positive and impactful culture.
This is a great opportunity for an experienced Secondary Care Specialist, apply now!
Please note:
+ Sponsorship is not available for this opportunity.
+ Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA.
#LI-DNI
#LI-CES
#LI-LK1
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Location:** Munster & Leinster, Republic of Ireland
**Position Type:** Field-based
An experienced Secondary Care Specialist is sought to join an established pharmaceutical sales team in the field of rheumatology. This strategic and promotional role focuses on driving product differentiation and uptake across key hospitals and clinical centres in Munster and Leinster.
The role involves leading product promotion to secondary care healthcare professionals, delivering professional presentations, and providing specialist medical education. The successful candidate will ensure that relevant decision-makers understand the clinical benefits of the products to support formulary access and funding.
A key aspect of the role is engaging and developing regional and national opinion leaders to build clinical experience and support therapy area education and access. The candidate will proactively communicate with customers through compliant channels including face-to-face visits, virtual meetings, phone calls, and emails. They will also collaborate with internal stakeholders to implement creative customer engagement initiatives aligned with business plans and strategic investments.
This position requires a high level of collaboration with the national sales and marketing teams and embraces the core values of the organization to contribute to a positive and impactful culture.
This is a great opportunity for an experienced Secondary Care Specialist, apply now!
Please note:
+ Sponsorship is not available for this opportunity.
+ Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA.
#LI-DNI
#LI-CES
#LI-LK1
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
4
Development Scientist
Waterford, Munster
Sanofi Group
Posted today
Job Viewed
Job Description
_Job Title: Development Scientist_
_Location: Waterford_
About Waterford
_For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing._
**About the job**
**Our Team:**
_The Manufacturing Sciences team, operating within the MSAT laboratory at Sanofi Waterford plays an integral role in new product introduction, technology transfer and supporting on-going lifecycle management activities for Sanofi Waterford and the wider Sanofi network. The team consists of passionate, data driven scientists who lead technical programs for a variety of complex biologics including enzyme replacement therapies and monoclonal antibodies. As a part of this team you will gain hands on experience with these products, developing manufacturing processes and working with cross functional teams to provide scientific expertise to ensure our products get to the patients who need them._
**Main responsibilities:**
· Directs and participates in process and product life cycle and development activities. Authors and reviews process development sections of regulatory and technical documents, study reports and technology transfer documents
· Establishes a comprehensive knowledge of the Critical Process Parameters, Critical Product Quality Attributes and Characteristics to provide SME support to the network
· Establishes analytical methods to support biophysical, solid state and primary packaging characterisation
· Designs, executes and documents technical studies to investigate product and process robustness, scale-up, stability and degradation pathways for therapeutic proteins
· Represents the Manufacturing Sciences department on cross functional teams across the Sanofi network delivering technical expertise and knowledge providing the link between R&D and Manufacturing
· Participates in collaborative research programs while also mentoring graduate and junior scientists helping them reach their full potential
**About you**
· MSc (Preferably by Research) or PhD in Pharmaceutical Science, Pharmaceutical Eng., Biotechnology, Biopharmaceutics, Pharmacy with relevant industry or post-doctorate experience.
· Strong technical knowledge in either Protein, Physical or Manufacturing Sciences
· Hands on experience performing product and process characterisation in a selected discipline
· Proteins - Structural Protein Chemistry (i.e., CD, FTIR, Fluorescence, UV-VIS) and aggregation (i.e., HPLC, DLS, Archimedes, MFI)
· Physical - Solid State (i.e., XRD, DSC, TGA, SEM, DVS)
· Manufacturing Sciences - Pumping, Mixing, Filling, Lyophilisation and CCIT
· Excellent oral and written communication skills with ability to influence at senior level
· Interest and passion for science contributing to an energised working environment
· Ability to quickly adapt to changes in project direction
· Technical expertise in either: Protein, Physical or Manufacturing Sciences
· Be able to drive change and find innovative ways of performing technical investigations
· Liaise transversally with peers at all levels throughout the Sanofi network
· Exhibit strong management competencies - providing strong scientific thinking and rationale
· It would be advantageous to have:
- Expertise in lyophilisation - Process and product development as well as equipment understanding
- Fundamental knowledge of the role of excipients in lyophilised and liquid biopharmaceuticals
- Demonstrated track record of peer-reviewed publications and academic contributions
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
_Location: Waterford_
About Waterford
_For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing._
**About the job**
**Our Team:**
_The Manufacturing Sciences team, operating within the MSAT laboratory at Sanofi Waterford plays an integral role in new product introduction, technology transfer and supporting on-going lifecycle management activities for Sanofi Waterford and the wider Sanofi network. The team consists of passionate, data driven scientists who lead technical programs for a variety of complex biologics including enzyme replacement therapies and monoclonal antibodies. As a part of this team you will gain hands on experience with these products, developing manufacturing processes and working with cross functional teams to provide scientific expertise to ensure our products get to the patients who need them._
**Main responsibilities:**
· Directs and participates in process and product life cycle and development activities. Authors and reviews process development sections of regulatory and technical documents, study reports and technology transfer documents
· Establishes a comprehensive knowledge of the Critical Process Parameters, Critical Product Quality Attributes and Characteristics to provide SME support to the network
· Establishes analytical methods to support biophysical, solid state and primary packaging characterisation
· Designs, executes and documents technical studies to investigate product and process robustness, scale-up, stability and degradation pathways for therapeutic proteins
· Represents the Manufacturing Sciences department on cross functional teams across the Sanofi network delivering technical expertise and knowledge providing the link between R&D and Manufacturing
· Participates in collaborative research programs while also mentoring graduate and junior scientists helping them reach their full potential
**About you**
· MSc (Preferably by Research) or PhD in Pharmaceutical Science, Pharmaceutical Eng., Biotechnology, Biopharmaceutics, Pharmacy with relevant industry or post-doctorate experience.
· Strong technical knowledge in either Protein, Physical or Manufacturing Sciences
· Hands on experience performing product and process characterisation in a selected discipline
· Proteins - Structural Protein Chemistry (i.e., CD, FTIR, Fluorescence, UV-VIS) and aggregation (i.e., HPLC, DLS, Archimedes, MFI)
· Physical - Solid State (i.e., XRD, DSC, TGA, SEM, DVS)
· Manufacturing Sciences - Pumping, Mixing, Filling, Lyophilisation and CCIT
· Excellent oral and written communication skills with ability to influence at senior level
· Interest and passion for science contributing to an energised working environment
· Ability to quickly adapt to changes in project direction
· Technical expertise in either: Protein, Physical or Manufacturing Sciences
· Be able to drive change and find innovative ways of performing technical investigations
· Liaise transversally with peers at all levels throughout the Sanofi network
· Exhibit strong management competencies - providing strong scientific thinking and rationale
· It would be advantageous to have:
- Expertise in lyophilisation - Process and product development as well as equipment understanding
- Fundamental knowledge of the role of excipients in lyophilised and liquid biopharmaceuticals
- Demonstrated track record of peer-reviewed publications and academic contributions
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
This advertiser has chosen not to accept applicants from your region.
5
zCX Developer
Waterford, Munster
IBM
Posted today
Job Viewed
Job Description
**Introduction**
Are you interested in developing operating systems and contributing to Open Source? Did you just graduate and are eager to become part of an worldwide development community? Is your favorite OS Linux based and you enjoy low-level programming? If so, our team is the right place for you! We are expanding our IBM development team in Waterford. The team is responsible for enhancing the Linux kernel for IBM Z / IBM LinuxOne. This includes device drivers, new processor instructions, virtualization (KVM), confidential containers, and test automation/devops (CI/CD).
**Your role and responsibilities**
As a key member of our team, you will play a vital role in crafting exceptional software experiences. Your responsibilities will include the design and specifications for new features, implementation of the design, identifying and bug fixing, performance analysis, submitting your code to upstream open source community repositories, and solving client problems. This position requires working onsite 3 days per week.
**Required technical and professional expertise**
* Minimum of 3 years professional experience working in containerized environments, e.g. based on Kubernetes or OpenShift.
* This includes low-level software development, as well as a solid understanding of container orchestration, deployment topologies, as well as virtualization techniques.
* Experience in source code repository systems (e.g. git), scripting languages (e.g. Python) and test Automation (e.g. Jenkins)
* Extensive experience with one of the following Python or GOLang.
* Extensive experience in AI and Machine Learning (Knowledge of LLMS and opens source versions like llama)
**Preferred technical and professional experience**
*
Any previous contributions to Open Source projects Skills in current I/O technologies (e.g. PCI, NVMe, RDMA) would be ideal
*
Experience in Z Architecture (S390X) and compilers would be a significant advantage
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
Are you interested in developing operating systems and contributing to Open Source? Did you just graduate and are eager to become part of an worldwide development community? Is your favorite OS Linux based and you enjoy low-level programming? If so, our team is the right place for you! We are expanding our IBM development team in Waterford. The team is responsible for enhancing the Linux kernel for IBM Z / IBM LinuxOne. This includes device drivers, new processor instructions, virtualization (KVM), confidential containers, and test automation/devops (CI/CD).
**Your role and responsibilities**
As a key member of our team, you will play a vital role in crafting exceptional software experiences. Your responsibilities will include the design and specifications for new features, implementation of the design, identifying and bug fixing, performance analysis, submitting your code to upstream open source community repositories, and solving client problems. This position requires working onsite 3 days per week.
**Required technical and professional expertise**
* Minimum of 3 years professional experience working in containerized environments, e.g. based on Kubernetes or OpenShift.
* This includes low-level software development, as well as a solid understanding of container orchestration, deployment topologies, as well as virtualization techniques.
* Experience in source code repository systems (e.g. git), scripting languages (e.g. Python) and test Automation (e.g. Jenkins)
* Extensive experience with one of the following Python or GOLang.
* Extensive experience in AI and Machine Learning (Knowledge of LLMS and opens source versions like llama)
**Preferred technical and professional experience**
*
Any previous contributions to Open Source projects Skills in current I/O technologies (e.g. PCI, NVMe, RDMA) would be ideal
*
Experience in Z Architecture (S390X) and compilers would be a significant advantage
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest All Jobs in Waterford !
6
Firmware Developer
Waterford, Munster
IBM
Posted today
Job Viewed
Job Description
**Introduction**
Are you interested in developing operating systems and contributing to Open Source? Did you just graduate and are eager to become part of an worldwide development community? Is your favorite OS Linux based and you enjoy low-level programming? If so, our team is the right place for you! We are expanding our IBM development team in Waterford. The team is responsible for enhancing the Linux kernel for IBM Z / IBM LinuxOne. This includes device drivers, new processor instructions, virtualization (KVM), confidential containers, and test automation/devops (CI/CD).
**Your role and responsibilities**
As a key member of our team, you will play a vital role in crafting exceptional software experiences. Your responsibilities will include the design and specifications for new features, implementation of the design, identifying and bug fixing, performance analysis, submitting your code to upstream open source community repositories, and solving client problems. This position requires working onsite 3 days per week.
**Required technical and professional expertise**
* Demonstrated Professional experience and understanding of operating systems internals (e.g. memory management & task scheduling, interrupts, device drivers) .
* Experience in source code repository systems (e.g. git), scripting languages (e.g. Python), and in developing automation for CI/CD pipelines.
* Experience in packaging and management of software components.
* Minimum of 3 years professional experience working on low-level software development
* Extensive experience with one of the following C/C++ or Assembly.
**Preferred technical and professional experience**
*
Any previous contributions to Open Source projects Skills in current I/O technologies (e.g. PCI, NVMe, RDMA) would be ideal
*
Any skills in IBM Z architecture ("Principles of Operations"), Z assembler and I/O concepts would be a bonus
*
Experience in Cryptography would be a significant advantage
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
Are you interested in developing operating systems and contributing to Open Source? Did you just graduate and are eager to become part of an worldwide development community? Is your favorite OS Linux based and you enjoy low-level programming? If so, our team is the right place for you! We are expanding our IBM development team in Waterford. The team is responsible for enhancing the Linux kernel for IBM Z / IBM LinuxOne. This includes device drivers, new processor instructions, virtualization (KVM), confidential containers, and test automation/devops (CI/CD).
**Your role and responsibilities**
As a key member of our team, you will play a vital role in crafting exceptional software experiences. Your responsibilities will include the design and specifications for new features, implementation of the design, identifying and bug fixing, performance analysis, submitting your code to upstream open source community repositories, and solving client problems. This position requires working onsite 3 days per week.
**Required technical and professional expertise**
* Demonstrated Professional experience and understanding of operating systems internals (e.g. memory management & task scheduling, interrupts, device drivers) .
* Experience in source code repository systems (e.g. git), scripting languages (e.g. Python), and in developing automation for CI/CD pipelines.
* Experience in packaging and management of software components.
* Minimum of 3 years professional experience working on low-level software development
* Extensive experience with one of the following C/C++ or Assembly.
**Preferred technical and professional experience**
*
Any previous contributions to Open Source projects Skills in current I/O technologies (e.g. PCI, NVMe, RDMA) would be ideal
*
Any skills in IBM Z architecture ("Principles of Operations"), Z assembler and I/O concepts would be a bonus
*
Experience in Cryptography would be a significant advantage
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
This advertiser has chosen not to accept applicants from your region.
7
Technical Lead - IBM Z Development
Waterford, Munster
IBM
Posted today
Job Viewed
Job Description
**Introduction**
Our mission is to expand our IBM Z development team in Waterford, Ireland.
We will integrate our team in the global IBM Z development community.
We will connect with regional IBM and RedHat teams.
We will closely work with academia, provide tailored IBM Z education at universities.
By performing Industrial Research, we will deliver crucial and highly innovative products to our enterprise clients and influence IBMs strategy for IBM Z multi-architecture deployments, Linux, and AI.
**Your role and responsibilities**
Technically lead IBM Z development teams.
The focus will be broad and include crucial Infrastructure enhancements for IBM Z, such as Linux kernel, multi-architecture deployments of IBM Z. It will also include AI solutions, which are built on these new infrastructure enhancements.
Provide guidance and mentor junior developers.
Actively support our developer profession certification.
Closely collaborate with other international leaders to plan and integrate our products.
Foster university relations and create content for lectures, tailored to our needs.
Interact with clients, technical sales colleagues, and product management to define development priorities.
Technically host and lead hiring interviews.
Work with RedHat leaders to enable a strong mutual collaboration.
This position is based in our Waterford location and requires working onsite 3 days per week.
**Required technical and professional expertise**
Linux Expertise and recent demonstrated experience with C/C++ low level programming.
Strong technical leadership including demonstrated experience in architecture boards, leadership/executive management interactions to define roadmaps and strategies for entire product stacks.
Broad experience from multiple technical leadership positions.
Strong teaching/educating capabilities for technical contents.
Strong network within IBM, universities, and clients.
**Preferred technical and professional experience**
Passion for IBM Z, Linux, and Open Source, and machine learning.
Experience in building new teams.
Quick comprehension in new technical areas.
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
Our mission is to expand our IBM Z development team in Waterford, Ireland.
We will integrate our team in the global IBM Z development community.
We will connect with regional IBM and RedHat teams.
We will closely work with academia, provide tailored IBM Z education at universities.
By performing Industrial Research, we will deliver crucial and highly innovative products to our enterprise clients and influence IBMs strategy for IBM Z multi-architecture deployments, Linux, and AI.
**Your role and responsibilities**
Technically lead IBM Z development teams.
The focus will be broad and include crucial Infrastructure enhancements for IBM Z, such as Linux kernel, multi-architecture deployments of IBM Z. It will also include AI solutions, which are built on these new infrastructure enhancements.
Provide guidance and mentor junior developers.
Actively support our developer profession certification.
Closely collaborate with other international leaders to plan and integrate our products.
Foster university relations and create content for lectures, tailored to our needs.
Interact with clients, technical sales colleagues, and product management to define development priorities.
Technically host and lead hiring interviews.
Work with RedHat leaders to enable a strong mutual collaboration.
This position is based in our Waterford location and requires working onsite 3 days per week.
**Required technical and professional expertise**
Linux Expertise and recent demonstrated experience with C/C++ low level programming.
Strong technical leadership including demonstrated experience in architecture boards, leadership/executive management interactions to define roadmaps and strategies for entire product stacks.
Broad experience from multiple technical leadership positions.
Strong teaching/educating capabilities for technical contents.
Strong network within IBM, universities, and clients.
**Preferred technical and professional experience**
Passion for IBM Z, Linux, and Open Source, and machine learning.
Experience in building new teams.
Quick comprehension in new technical areas.
IBM is committed to creating a diverse environment and is proud to be an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, caste, genetics, pregnancy, disability, neurodivergence, age, veteran status, or other characteristics. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
This advertiser has chosen not to accept applicants from your region.
8
Lead - Packaging Technology (all genders)
Waterford, Munster
Sanofi Group
Posted 2 days ago
Job Viewed
Job Description
**To ensure a rapid processing of your application, please apply only via the "Apply" button. Please include a letter of motivation and a current resume with your application.**
**_About the job_**
Sanofi's Global Medical Device and Packaging organization aims to lead the industry in device-mediated therapies, developing best-in-class drug delivery systems and connected medical devices. The team focuses on innovative, user-centric, and environmentally sustainable solutions that enhance drug administration and improve patient outcomes.
The role involves working with cross-functional teams, manufacturing sites, and external suppliers to develop and implement robust manufacturing solutions for drug-device combination products and vial products, with a focus on secondary packaging processes.
This position is critical for maintaining Sanofi's position at the forefront of drug delivery technology while ensuring efficient, sustainable, and compliant manufacturing processes.
We look forward to your application!
**Core Responsibilities of this role:**
**Strategic Leadership:**
+ Lead secondary packaging manufacturing strategy for drug delivery systems
+ Manage packaging engineering team
+ Serve as main interface with stakeholders, manufacturing sites, and suppliers
+ Drive global technical investigations
**Technical Development:**
+ Guide manufacturing concept development and technology solutions
+ Participate in design reviews and risk assessments
+ Lead new product introductions and process development
+ Develop manufacturing strategies and equipment specifications
**Project Management:**
+ Oversee project execution from design to qualification
+ Support technology transfer and implementation
+ Lead platform standardization and improvement initiatives
+ Drive sustainability and cost-effectiveness improvements
**Innovation & Problem Solving:**
+ Support root cause analysis and manufacturing investigations
+ Implement process improvements using Lean Six Sigma
+ Stay current with industry best practices
+ Explore and implement next-gen manufacturing technologies
**_About you_**
**Education**
+ Bachelor's degree in packaging, mechanical engineering, or relevant engineering discipline. Advanced degree a plus
**Experience** :
+ Several years experience in Medical Device, Pharmaceutical, or Biotechnology industry
+ Deep packaging design, process development, and manufacturing experience required
+ Thorough knowledge of primary and secondary component materials/systems, pharmaceutical package testing, packaging line equipment, printing, and vision control systems
+ Knowledge of device and packaging regulations, quality systems, design fundamentals of combination products, design controls, design transfer, and manufacturing process validation
+ Manufacturing Program Lead of larger projects, proven track record developing manufacturing strategy, providing technical leadership and managing cross-functional teams in execution.
**Soft skills** :
+ Self-motivated and results oriented
+ Ability to influence and negotiate to desired outcome
+ Drives decision-making processes with stakeholders inside and outside own perimeter
+ Actively takes decisions within scope of responsibility, and is accountable for results
+ Presentation and communication skills to influence decision making at senior levels
+ Builds relationships and strong partnerships with stakeholders across the organization
+ Has a global mindset and the ability to think strategically
**Technical skills** :
+ Proven expertise in pharmaceutical manufacturing, GxP documentation and related Equipment Qualification and Process Validation of high throughput equipment.
+ Strong technical skills and familiarity with competitive landscape, industry trends, and regulatory environment.
+ Strong analytical, problem solving, and technical writing skills,
+ Working competency of statistical programs (e.g. Minitab, SAS)
**Languages**
+ Fluent in English, French or German basic knowledge is a plus
**_Why choose us?_**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
+ We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.
+ Start your career at an attractive location in the center / in the capital of Germany and experience our modern working environment and benefit from hybrid, flexible working time models.
**Pursue** **_Progress_** **. Discover** **_Extraordinary_** **.**
Progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let's pursue progress. And let's discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
#Sanofi
#SanofiCareers
#PursueProgress ( **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
**_About the job_**
Sanofi's Global Medical Device and Packaging organization aims to lead the industry in device-mediated therapies, developing best-in-class drug delivery systems and connected medical devices. The team focuses on innovative, user-centric, and environmentally sustainable solutions that enhance drug administration and improve patient outcomes.
The role involves working with cross-functional teams, manufacturing sites, and external suppliers to develop and implement robust manufacturing solutions for drug-device combination products and vial products, with a focus on secondary packaging processes.
This position is critical for maintaining Sanofi's position at the forefront of drug delivery technology while ensuring efficient, sustainable, and compliant manufacturing processes.
We look forward to your application!
**Core Responsibilities of this role:**
**Strategic Leadership:**
+ Lead secondary packaging manufacturing strategy for drug delivery systems
+ Manage packaging engineering team
+ Serve as main interface with stakeholders, manufacturing sites, and suppliers
+ Drive global technical investigations
**Technical Development:**
+ Guide manufacturing concept development and technology solutions
+ Participate in design reviews and risk assessments
+ Lead new product introductions and process development
+ Develop manufacturing strategies and equipment specifications
**Project Management:**
+ Oversee project execution from design to qualification
+ Support technology transfer and implementation
+ Lead platform standardization and improvement initiatives
+ Drive sustainability and cost-effectiveness improvements
**Innovation & Problem Solving:**
+ Support root cause analysis and manufacturing investigations
+ Implement process improvements using Lean Six Sigma
+ Stay current with industry best practices
+ Explore and implement next-gen manufacturing technologies
**_About you_**
**Education**
+ Bachelor's degree in packaging, mechanical engineering, or relevant engineering discipline. Advanced degree a plus
**Experience** :
+ Several years experience in Medical Device, Pharmaceutical, or Biotechnology industry
+ Deep packaging design, process development, and manufacturing experience required
+ Thorough knowledge of primary and secondary component materials/systems, pharmaceutical package testing, packaging line equipment, printing, and vision control systems
+ Knowledge of device and packaging regulations, quality systems, design fundamentals of combination products, design controls, design transfer, and manufacturing process validation
+ Manufacturing Program Lead of larger projects, proven track record developing manufacturing strategy, providing technical leadership and managing cross-functional teams in execution.
**Soft skills** :
+ Self-motivated and results oriented
+ Ability to influence and negotiate to desired outcome
+ Drives decision-making processes with stakeholders inside and outside own perimeter
+ Actively takes decisions within scope of responsibility, and is accountable for results
+ Presentation and communication skills to influence decision making at senior levels
+ Builds relationships and strong partnerships with stakeholders across the organization
+ Has a global mindset and the ability to think strategically
**Technical skills** :
+ Proven expertise in pharmaceutical manufacturing, GxP documentation and related Equipment Qualification and Process Validation of high throughput equipment.
+ Strong technical skills and familiarity with competitive landscape, industry trends, and regulatory environment.
+ Strong analytical, problem solving, and technical writing skills,
+ Working competency of statistical programs (e.g. Minitab, SAS)
**Languages**
+ Fluent in English, French or German basic knowledge is a plus
**_Why choose us?_**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
+ We take care of you and your family with a wide range of health and social such as high-quality healthcare, numerous prevention programs and coverage for long-term illness. Our 14-week paid family leave for both parents is outstanding as well as a wide range of childcare benefits.
+ Start your career at an attractive location in the center / in the capital of Germany and experience our modern working environment and benefit from hybrid, flexible working time models.
**Pursue** **_Progress_** **. Discover** **_Extraordinary_** **.**
Progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let's pursue progress. And let's discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
#Sanofi
#SanofiCareers
#PursueProgress ( **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
This advertiser has chosen not to accept applicants from your region.
9