108 Jobs in Sligo

Visual Inspection Engineer

Sligo, Connacht AbbVie

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Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Join our dynamic team at AbbVie in Sligo as a Visual Inspection Engineer! This is an excellent opportunity for a driven engineering or science professional with a passion for quality, continuous improvement, and making a difference in healthcare.
Key Responsibilities:
- Support Visual Inspection operations to meet all safety, regulatory, and organizational standards.
- Develop and optimize procedures to enhance manufacturing processes.
- Participate in process, equipment, and facilities validation projects; review and execute commissioning and validation protocols to keep projects on schedule.
- Support the introduction of new Semi Automate visual inspection equipment on site and associated training
- Lead and facilitate FMEAs for Visual Inspection, and drive the certification of technicians.
- Build and maintain defect libraries and execute trending for defect analysis.
- Ensure local procedures align with global guidelines and regulatory expectations.
- Provide technical leadership and guide the development of SOPs for visual inspection.
- Collaborate with internal and external stakeholders to evaluate particles/defects and support technical transfers for new product introductions.
- Investigate process deviations and support the production team in achieving output and yield targets.
- Ensure full compliance with quality, safety, cGMP, and regulatory policies.
- Supervise external contractors as required.
Qualifications
- Hold a Level 8 degree (or higher) in Engineering, Science, or a relevant technical discipline.
- Minimum 3 years' experience in a biotech or pharmaceutical manufacturing environment-experience with biotechnological drug processes, fill finish, lyophilisation, and sterilisation preferred.
- Strong problem-solving and innovative thinking skills under pressure.
- Familiarity with Semi Automated Visual inspection equipment
- Exceptional attention to detail and commitment to quality.
- Excellent communication and interpersonal skills; proven ability to work both independently and in cross-functional teams.
- Leadership qualities with a results-driven mindset.
- Demonstrate integrity, a strong work ethic, and the ability to work autonomously.
- Familiarity with cGMP, ISO, FDA regulations, and EHS best practices preferred.
Additional Information
What We Offer: A collaborative and innovative environment where your work impacts patients lives, opportunities for personal and professional development, and a chance to lead quality improvements in cutting-edge biologics manufacturing.
How to Apply: Ready to take the next step in your career? Apply now to join AbbVie and contribute to our mission in delivering best-in-class healthcare solutions
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
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Technician, Warehouse

Sligo, Connacht AbbVie

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Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
What you do, is what we need. Making a difference begins here. And takes all of us.
Welcome to AbbVie!
We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.
Here in AbbVie, Ballytivnan are looking for a Warehouse Technician to join their team. You will be working alongside a team of 4 and support the Supply Chain Manager in line with all safety, regulatory and organisational requirements. All necessary training will be provided although previous experience in a similar role would be an advantage.
Your responsibilities will include:
+ Ensuring raw materials are checked, verified and booked in as per procedures.
+ Ensuring supply items are checked, verified and booked in as per procedures.
+ Completing receiver documentation for non-inventory purchased items.
+ Managing inventory and purchase of supply items within the warehouse.
+ Completing invoice documentation for finished product shipments.
+ Liaising with freight companies to arrange finished product shipments.
+ Distribution of post and courier deliveries within the site.
+ Coordination of courier shipments within the site.
+ Ensuring engineering stores deliveries are verified and booked in as per procedures
+ Manage the segregation and collection of recycling and waste at the site.
+ Maintain supply of materials to production.
Qualifications
Qualifications
List required and preferred qualifications (up to 10). Include education, skills and experience.
+ Certificate / Diploma qualification in suitable Logistics /science/engineering course is desirable but not essential and/or suitable experience.
+ 1 year experience in Batch processing operations in an FDA/ HPRA regulated industry coupled with 1 year Experience with safe handling of dangerous chemicals is desirable. Knowledge of cGMP and regulatory requirements relating to the pharmaceutical or similar industry is desirable.
+ The position requires the knowledge of national and international regulations for the safe transportation of hazardous materials including label codes, documentation, licence etc.
+ Good IT skills are required for this position.
+ Requires a high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times.
+ Strong communication skills both verbal and written are required for the execution of this role.
+ Requires total commitment to quality and maintaining a high standard of work at all times.
+ The position requires a moderate level of manual work, in the movement, charging and discharging of raw materials and finished products. All personnel must be able to accomplish these manual tasks, while wearing appropriate PPE.
Additional Information
What you will need:
+ 2 years previous Warehouse experience in a regulated environment is an advantage
+ Computer skills
+ Good interpersonal and communication skills
+ Excellent planning and organisational skills
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
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Account Executive - North West

Sligo, Connacht Diageo

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**Job Description :**
**Job Title** Account Executive
**Location:** North West ( Roscommon, Leitrim and Sligo)
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!
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 apply for the role of Account Executive for Dublin City. 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 Approach:** 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 leverage digital 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
**OUR OFFER**
+ An inclusive company culture that puts employees and their development first
+ A competitive salary with bonus and many benefits
+ Growth opportunities
+ A great family leave policy .and of course, THE best colleagues!
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 (
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Buyer/Planner

Sligo, Connacht Abbott

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**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Abbott in Ireland**
Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo.
**Abbott Ireland Nutrition Sligo**
We understand that proper nutrition is the foundation for living the best life possible. That's why we develop science-based nutrition products for people of all ages. Our products help babies and children grow, keep bodies strong and active, and support the unique nutrition needs of people with chronic illnesses - to make every stage of life a healthy one.
Abbott is a leader in providing enteral nutrition feeding devices, including enteral feeding pumps and pump sets. Enteral feeding (also known as tube feeding) is a means of providing nutrition to people who cannot obtain nutrition by swallowing. Enteral nutrition contains all the calories and vitamins a person needs.
Abbott's journey in Ireland began in 1974 with our first manufacturing facility in Sligo. Over the years, we've transformed from manual operations to a state-of-the-art, fully automated facility. Now located in Carbury Point, Finisklin, Sligo, our award-winning site is recognized for operational excellence, safety, training, and community involvement. The prestigious Shingo Prize for Operational Excellence highlights our commitment to continuous improvement and a culture of excellence, delivering sustainable results year after year.
**Primary Function / Goals / Objectives**
Reporting to the Planning and Purchasing Manager, your key responsibilities will include:
+ Responsibility for MPS & MRP for raw material, intermediate and finished goods.
+ Manage the Purchasing function to ensure material supply in line with plant schedules.
+ Coordinate the purchasing process and work with NPI activities.
+ BOM / Item Master Management
+ CRM and primary point of contact for distribution centre
+ Scenario planning
+ Coordinate materials aspect for NPI's
+ Work with Supply chain members to meet target performance on KPIs
+ Inventory Management and Control(including cycle count process)
+ Liaise with transportation companies regarding deliveries
+ Schedule deliveries within warehouse capacities
+ Project implementation in line with specific goals
+ The position will require communication with the following:
+ Contacts with all levels of management within the plant.
+ Contacts with Abbott personnel in other affiliates especially in planning shipping/distribution/marketing.
+ Coordinate purchased materials to support production and meet product cost within the framework of Abbott Code of Business and applicable laws.
+ Co-ordinate purchase of non-inventory items required to meet plant operation at lowest total cost of ownership levels
**Education/Skills/Knowledge:**
+ Certificate/Diploma/Degree in a related discipline, or IPICS / IIPMM. Appropriate qualification in either Purchasing/ Production Planning e.g. Diploma in Purchasing or relevant APICS (American Production and Inventory Control Society) examinations.
+ Excellent Computer skills.
+ Excellent planning and organizational skills.
+ Excellent communication & interpersonal skills
+ Excellent attention to detail.
+ Appropriate qualification in either Purchasing/ Production Planning e.g. Diploma in Purchasing or relevant APICS (American Production and Inventory Control Society) examinations.
+ At least two years' experience in production planning in a manufacturing company, preferably previous experience with planning short shelf life products.
+ A high level of expertise is required in solving scheduling, logistics, expediting and purchasing problems.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Senior Medical Safety Analyst

Sligo, Connacht Abbott

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**FIXED TERM CONTRACT**
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Nutrition**
Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.
**PURPOSE OF THE JOB**
As an individual contributor, with guidance from manager/team, functions to support Medical Safety & Surveillance (MSS) by reviewing, assessing, and summarizing medical device complaint information for complex investigations and risk assessments. Critically assess aggregate safety data from medical devices and communicates findings to internal stakeholders. Independently creates and delivers device medical safety training to a Global audience. Drafts documentation, including data reviews, clinical evaluations, literature reviews and standard operating procedures.
**MAJOR RESPONSIBILITIES**
+ Create and present medical safety related analyses, reports, and/or assessments orally and/or in writing within/ outside the Medical Safety and Surveillance department
+ Gather, critically analyze, and present findings from Medical Safety and Surveillance complaint data on a periodic basis. Including tracking and trending activities.
+ Ensures adherence to departmental standard operating procedures (SOPs), and draft new SOP as needed.
+ Comfortable developing Medical Safety and Surveillance training materials and have strong presentation skills to provide training to a broad international audience.
+ May write or assist in preparing, completing literature or website searches and data analysis for regulatory documentation supporting medical device registration.
+ Conduct periodic literature searches, summarize findings and present information to a cross-functional team.
+ Will act as a back up to colleagues on day-to-day medical device complaints processing and conduct medical follow up calls to customers as needed to obtain adverse event and/or complaint details
+ As needed, determine complaint reportability to the competent authority; drive on-time vigilance reporting within regulatory time-frames
+ Other duties/projects/support as assigned.
**EDUCATION & COMPETENCIES**
+ Bachelor of Science, a Health science related background is a plus, such as dietitian, pharmacist, nurse etc.
+ RAC certification a plus
+ 2-3 years Medical Device experience in activities such as aggregate data review, Risk Assessment, DFMEA review, and patient safety
+ Data analytics / strong excel, PowerBI and/or data visualization skills
+ Medical knowledge to apply critical thinking and data analysis to Medical Safety data and/or Medical Device risk assessments.
+ Basic understanding of Global Medical Device regulations (primarily EUMDR, MedDEV), clinical research, and international guidelines/ standards related to medical devices (ISO, GSPR, MDGC etc.)
+ Willingness to learn other applicable Medical Device regulations, standards and guidelines
+ Drive to adhere to standard operating procedures (SOPs)
+ Strong ability /experience in presenting medical and scientific training/ data orally and in writing
+ Computer proficient (Windows, Word, Excel)
+ Enjoys working in a collaborative environment and with a multidisciplinary, Global team.
+ Works independently
Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Medical Devices Global Regulatory Documentation Manager

Sligo, Connacht Abbott

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**FIXED TERM CONTRACT**
**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford, and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations, and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
**Abbott Nutrition**
Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.
**PURPOSE OF THE JOB**
As a Medical Safety & Surveillance (MSS) Global Medical Device Manager, the candidate will use his/her in-depth understanding of medical devices to ensure compliance with regulatory requirements for Abbott Nutrition medical devices. The MSS Global Medical Device Manager will have responsibility for generating documentation that supports Abbott Nutrition's global medical device registration and on-going compliance with EUMDR. This may include development and implementation of global standardized operating procedures. The candidate may also lead the development/maintenance of local medical device vigilance systems (predominantly for UK and EU), ensuring compliance with local regulations. The candidate will have departmental, cross functional, and global influence, and will be considered a medical device subject matter expert within the company.
**MAJOR RESPONSIBILITIES**
+ Organizes, manages and maintains a highly compliant global medical device system for Abbott Nutrition.
+ Maintains awareness and ensures compliance with established and updated local and global medical device processes as well as local and global regulations and guidelines for medical device registration and post-market documentation.
+ Develops and implements training programs for individuals involved in medical device activities.
+ Monitors medical device system performance; tracks compliance metrics and reports to global MSS Leadership Team.
+ Ensures global/local medical device audit readiness; Supports medical device audits/inspections and leads activities related to corrective and preventative actions for any audit findings.
+ Actively contributes to activities related to the monitoring of safety profiles for Abbott Nutrition products registered as medical devices, such as signal detection, evaluation, and prioritization.
+ Reviews and provides input to product DFMEAs.
+ Assists local staff with drafting and implementation of Safety Data Exchange Agreements, if applicable.
+ Works cross-functionally with Regulatory Affairs and Quality Assurance functions to maintain current knowledge of regulatory safety reporting guidelines and implementing relevant guidelines into practices and procedures.
+ Assists in the preparation, review and submission of aggregate safety reports.
+ Accountable for strategic preparation of medical device regulatory submission documentation (i.e. CEP, CER, PSUR, PMCF etc) and on-time completion of these activities for the division.
**EDUCATION & COMPETENCIES**
+ Master's degree in related health science or equivalent skills, education, or experience.
+ RAC certification is a plus.
+ 5-7 years of experience and proficiency in medical device regulatory submissions to Notified Bodies under EUMDR / MedDEV and knowledge of Medical Device standards and guidelines (such as ISO, GSPR, and MDGC).
+ Solid understanding and working knowledge of medical device regulatory requirements and in the development and implementation of processes to maintain compliance.
+ Strong medical knowledge and understanding to support safety related activities; background/experience with nutrition/nutritional products is a plus.
+ Knowledge of Vigilance reporting regulations on a Global scale.
+ Minimum 3 years of experience in leading complex projects or programs; global/regional experience desirable.
+ Fluency in spoken/written English;
+ Computer proficient (Windows, Word, Excel); experience working in adverse event databases.
+ Excellent communication and interpersonal skills, both written and spoken.
+ Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects.
+ Strong commitment to compliance with the relevant rules and procedures and to scientific quality and integrity.
+ High level of accountability and reliability.
+ Demonstrates ability to work productively as a team.
+ Ability to work in a fast paced, changing environment.
+ Ease of operating in high stress, big decision situations.
+ Continuous improvement mindset.
+ Ability to influence a team in a positive way in relation to performance, change, and culture.
+ Demonstrate broad knowledge of Abbott's business and how department processes/responsibilities interconnect.
+ Mastery of the inventory deployment planning process.
+ Exceptional problem-solving skills
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Internship Science

Sligo, Connacht Abbott

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Unlock your potential as an Abbott Intern. Join us to work on impactful projects, learn from senior leaders, and build your career. Here you can:
+ Contribute to meaningful, challenging projects with a direct impact on our business
+ Have regular access to senior leadership providing you with an opportunity to grow and learn from the best each day
+ Develop your career and grow your knowledge through targeted training, a global intern community, and the opportunity to build your network
+ Access perks that keep you supported both inside and outside the office
**The Opportunity**
Our Interns provides a meaningful, professional, hands-on experience to students with proven academic performance and leadership potential. We hire students majoring in Science into our programs based on business needs. Ideal candidates will combine technical and business knowledge with analytical strength and creative problem-solving abilities.
Abbott's global business offers opportunities to work across a range of fields, which may include the following areas, along with additional activities depending on business needs:
**Science:**
+ Design of experiments, root cause analysis
+ Literature searches & data analytics to support the technical product support team
+ Analytical Lab Testing and Project work
+ Operations Performance
+ Customer Support
+ Product Support
+ Design Plan Change Management
+ Control Upgrades
+ Meter Installation
**Quality:**
+ Plant Quality Assurance
+ Division Quality Assurance
+ Division Regulatory Affairs
+ Corporate Quality Assurance and Division Quality Assurance
**What are we looking for?**
Eligible applicants should be:
+ Available for a 6, 9 or 12month placement to start between January to June 2026 (aligned with academic work placements dates)
+ Internship placements may be during or at the end of your undergraduate or post graduate course.
+ Pursuing a relevant third level undergraduate or post graduate qualification in a.
+ Candidates must be tracking to or have a minimum of 2.1 Grade in their undergraduate course.
+ Excellent communicators, team players and Innovators.
+ Passionate about STEM and interested in pursuing a career in a STEM environment.
+ A flexible and innovative approach to work.
+ Flexibility to be based at one of our Abbott sites listed above
**Locations:**
Cavan, Galway, Longford, Sligo, Tipperary
Career growth and future opportunities are pillars of our program. Students who continuously excel in our early career programs are encouraged to apply for Abbott's Professional Development Programs or other full-time positions.
For further information on our company please visit our website at Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Principal Project Engineer

Sligo, Connacht Abbott

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**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader, and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Sligo & Kilkenny and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**This is how you can make a difference at Abbott:**
We are interested in a **Principal Project Engineer** to lead innovative projects, drive cross-functional collaboration, and shape the future of our technical capabilities.
**Responsibilities:**
+ Lead and execute medium-scale, cross-disciplinary engineering projects with custom, risk-managed plans.
+ Translate customer, business, and technical needs into actionable project scopes and strategies.
+ Conduct feasibility studies and economic analyses to guide decision-making and optimize life cycle costs.
+ Benchmark internally and externally to inform strategic planning and continuous improvement.
+ Design and analyze experiments using diverse data sources to address strategic questions.
+ Develop and implement complete solutions that integrate regulatory, operational, and cost considerations.
+ Ensure quality and effectiveness of key engineering processes through sound design and risk mitigation.
+ Evaluate the impact of design changes and proactively manage potential failure modes.
+ Apply proven methodologies to enhance engineering processes and outcomes.
+ Serve as a technical liaison for internal teams and external stakeholders, including senior leadership.
+ Communicate effectively across various media and organizational levels.
+ Foster collaborative, respectful relationships with colleagues, vendors, and partners.
+ Uphold all Environmental, Health, Safety, and Energy (EHS&E) standards and engineering governance policies.
**Education and Experience:**
+ A Bachelor's degree in Engineering, Science, or a closely related field is preferred. Equivalent technical experience with demonstrated competence will also be considered.
+ A post-graduate degree is desirable and may contribute toward the required experience.
+ A minimum of 6 years of significant engineering and/or operational experience.
+ Proven track record of technical contributions and accomplishments in product or process development.
+ Strong technical knowledge and application of engineering principles and practices.
+ Experience leading and influencing cross-functional teams.
+ Recognized as a subject matter expert in a relevant technical discipline.
+ Background in healthcare, nutritional products, diagnostics, medical devices, pharmaceuticals, or similar industries is advantageous.
+ Demonstrated financial acumen and experience with fiscal control systems.
+ Demonstrated a sound knowledge of injection moulding, tool design, validation activities for medical device components
+ Demonstrated a clear strategy for performance improvements at suppliers for production output, improve quality, support CAPA activities and monitored for effectiveness.
**What we Offer**
Attractive compensation package that includes competitive pay, as well as benefits such as
+ Family health insurance,
+ Excellent pension scheme
+ Life assurance
+ Career Development
+ Fantastic new facility
+ Growing business plus access to many more benefits.
Connect with us at and on LinkedIn , Facebook ( , Instagram , X ( and YouTube .
Abbott is an equal opportunities employer.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.

Abbott Professional Development Program Operations (OPDP) - Ireland

Sligo, Connacht Abbott

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Our Operations Professional Development Program (OPDP) is an entry-level, three-year rotation program designed to offer hands-on experience while promoting personal and professional growth. As a participant from Ireland, you will begin the program and first two rotations in your home country, then you will complete your final-year rotation abroad.
We currently have a number of open positions on our OPDP Program in Ireland.
Upon completion, PDP participants graduate into their next full-time position in their home country, continuing to grow their career and contributing as an Abbott professional using the foundation of skills, experience and network developed during their time in the program.
**As a OPDP participant you will:**
· Be a regular full-time employee of Abbott and qualify for the same competitive salary and benefits as other Abbott employees.
· Assume full responsibility and contribute as a functional operation professional.
· Rotate through three challenging, demanding, and diverse assignments.
· Develop a well-rounded skill set through assignments in the established learning tracks (see below) for the program.
· Relocate to various sites around Ireland to experience assignment diversity and operations
· Work within multiple business units during your rotational program at Abbott.
· Have the opportunity to explore possible crossover assignments within other Operation Programs (i.e. Engineering, Manufacturing, Quality, Operational Excellence).
· Be paired with a mentor to assist in the development of your operations career.
· Create a personalized growth plan to serve as a step-by-step guide towards the experiences, knowledge, and resources necessary to achieve your career goals
· Obtain training customized to support your individual growth and development.
· Report to a department manager in each assignment who will oversee your day-to-day responsibilities.
**OPDP rotation overview:**
· In Ireland, the OPDP rotation is based on 12month rotations in the first two of three years. Your rotations will involve working across functional areas - Technical, Operations Planning, Quality Assurance, Project Management and Engineering.
· No assignment is repeated; each is with a different Assignment Manager
· OPDP participants starting the program in July 2026 will complete a three-year program with the final international (overseas) rotation ending in June 2029
**Requirements:**
+ Bachelor's Degree/master's in Engineering  (Automation / Mechanical / Electrical /  Automation) Biotechnology, Pharmacy, Food Science, Supply Chain (Business Studies with major/minor Supply Chain) or related disciplines (grade 2:1 or higher)
+ Tracking to or have a minimum of 2.1 Grade in your undergraduate course with a track record of outstanding co-curricular activities
+ Interest in pursuing a career in Operations - Production, Engineering, Plant Quality, etc.
+ Geographically mobile and willing to do at least one year assignment outside of home country
+ Unrestricted authorization to work in home country (within Europe)
+ Fluent level of English for written and verbal business communication.
**Key Skills**
+ Cpacity to apply skills and knowledge to address operational challenges and add value to the business.
+ Strong analytical and problem-solving skills.
+ Strong interpersonal, leadership & communication skills.
+ Eager to learn and has the flexibility and willingness to work on different projects.
+ Previous work experience in internship or co-op work experience would be an advantage
The closing date for applications is **Friday, 10 October 2025** . However, interviews will be conducted on a rolling basis from the launch of the program. We strongly encourage students to apply as early as possible to avoid missing out on these exciting opportunities.
#earlycareers
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
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Manager, Quality Control

Sligo, Connacht AbbVie

Posted 2 days ago

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Job Description

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
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