What Quality Control Technician Jobs are in Ireland?
Showing 88 Quality Control Technician jobs in Ireland
Job Description
12 month Stryker contract with full benefits.
Will work within the microbiology team, under general supervision, with responsibility to ensure effective and efficient sterility practices, which includes, but not limited to the following:
+ Environmental monitoring of cleanrooms for viable air, viable surface and particulate in line with ISO 14644 standards.
+ Monitoring of utilities including all grades of water, and where necessary, compressed air.
+ Co-ordination of samples for bioburden and endotoxin testing.
+ Ordering consumables (media etc) and general stock for day-to-day running of laboratory.
+ Applying cGLP to all laboratory activities including stock control.
+ Performing sampling for validations and re-qualifications as required. Review of validation files for compliance.
+ Strong interactions, maintainance and support of sterility suppliers.
+ Interact with Supplier quality team with respect to vendor sterility topics.
+ Interpreting sampling and monitoring data, applies statistical and analysis techniques, to determine control and trending.
+ Leads NC and CAPA generation and resolution within the Microbiology group and across related business units. Strong competency in troubleshooting, correction of NC and root cause analysis.
+ Performs sterility release review, interpreting data and trends.
+ Performs sterilisation validations and re-qualifications in line with relevant BS EN ISO standards.
+ Continually identifies opportunity for stabilization of trends, statistical control of processes to allow cost saving.
+ Mentors and trains team and cross functional groups as required (induction, GMP etc)
+ Subject matter expert to internal & external regulatory requirements, (including but not limited to European RHQ, Division, Corporate, FDA, ISO, MDD, and individual country regulatory requirements)
+ Subject matter expert to local procedures, contribute to the development, maintenance and improvements of the policies and procedures to align to best practices, benchmarking against industry leads and regulatory requirements.
+ Coach, mentor and train other functions in area of sterility and monitoring.
+ Support of, ensure compliance of new products to sites' sterility standards. Successful integration of products to validated processes.
+ Ensures biocompatible of components, materials and consumables used in the manufacture of Stryker product.
**What you will need:**
. Bachelor degree/ Masters of Microbiology (Level 8)
. 2 years Microbiology related experience.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Will work within the microbiology team, under general supervision, with responsibility to ensure effective and efficient sterility practices, which includes, but not limited to the following:
+ Environmental monitoring of cleanrooms for viable air, viable surface and particulate in line with ISO 14644 standards.
+ Monitoring of utilities including all grades of water, and where necessary, compressed air.
+ Co-ordination of samples for bioburden and endotoxin testing.
+ Ordering consumables (media etc) and general stock for day-to-day running of laboratory.
+ Applying cGLP to all laboratory activities including stock control.
+ Performing sampling for validations and re-qualifications as required. Review of validation files for compliance.
+ Strong interactions, maintainance and support of sterility suppliers.
+ Interact with Supplier quality team with respect to vendor sterility topics.
+ Interpreting sampling and monitoring data, applies statistical and analysis techniques, to determine control and trending.
+ Leads NC and CAPA generation and resolution within the Microbiology group and across related business units. Strong competency in troubleshooting, correction of NC and root cause analysis.
+ Performs sterility release review, interpreting data and trends.
+ Performs sterilisation validations and re-qualifications in line with relevant BS EN ISO standards.
+ Continually identifies opportunity for stabilization of trends, statistical control of processes to allow cost saving.
+ Mentors and trains team and cross functional groups as required (induction, GMP etc)
+ Subject matter expert to internal & external regulatory requirements, (including but not limited to European RHQ, Division, Corporate, FDA, ISO, MDD, and individual country regulatory requirements)
+ Subject matter expert to local procedures, contribute to the development, maintenance and improvements of the policies and procedures to align to best practices, benchmarking against industry leads and regulatory requirements.
+ Coach, mentor and train other functions in area of sterility and monitoring.
+ Support of, ensure compliance of new products to sites' sterility standards. Successful integration of products to validated processes.
+ Ensures biocompatible of components, materials and consumables used in the manufacture of Stryker product.
**What you will need:**
. Bachelor degree/ Masters of Microbiology (Level 8)
. 2 years Microbiology related experience.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
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0
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier, cleaner, and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Effective communication of evidence and information is essential to conveying the value of products. Our highly trained staff provide medical writing services for the peri- and post-approval phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standards, and corporate guidance.
**Discover Impactful Work**
The Publications and Scientific Communications team, part of the Medical Writing and Healthcare Communications department at Thermo Fisher Scientific, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**What You'll Do in the Role**
+ Write, edit, and manage **manuscripts, posters, abstracts, oral presentation slide decks, and review articles** , on time, within budget, and with little instruction
+ Raise and help resolve project management issues, such as out-of-scope requests
+ Ensure compliance with quality processes and industry standards
+ Represent the team as the lead contact on projects
+ Lead or provide input on process improvements
**Keys to Success**
We are looking for an expert publication writer to join the team. The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have extensive experience in creating publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek a bright teammate who is proactive, enjoys challenges, and can thrive in a highly collaborative CRO (contract research organization) environment.
**Education, Experience & Skills**
+ Extensive proven experience as a writer of peer-reviewed medical publications
+ Experience working in a CRO environment preferred
+ Experience of generating publication extenders (e.g., plain language summaries, video/graphical abstracts) advantageous
+ Experience of publication planning/strategy advantageous
+ Excellent scientific writing, project management, and digital literacy
+ Bachelor's degree or higher in a scientific field; advanced degree preferred
+ In-depth knowledge of different therapeutic areas
+ Additional qualifications (e.g., EMWA or CMPP certification) advantageous
+ Sound professional judgement in dealing with inquiries, issues, and customer concerns
+ Able to independently make decisions and solve problems
+ Comfortable working on multiple projects concurrently
+ Able to prioritize and delegate tasks effectively
+ Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
**Physical Requirements / Work Environment**
+ Work will be 100% remote (home based)
+ Occasional domestic and international travel may be required
**Why Join Us?**
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other legally protected status.
**NOTE: Please include in your application a cover letter describing your qualifications for the role.**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier, cleaner, and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Effective communication of evidence and information is essential to conveying the value of products. Our highly trained staff provide medical writing services for the peri- and post-approval phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standards, and corporate guidance.
**Discover Impactful Work**
The Publications and Scientific Communications team, part of the Medical Writing and Healthcare Communications department at Thermo Fisher Scientific, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**What You'll Do in the Role**
+ Write, edit, and manage **manuscripts, posters, abstracts, oral presentation slide decks, and review articles** , on time, within budget, and with little instruction
+ Raise and help resolve project management issues, such as out-of-scope requests
+ Ensure compliance with quality processes and industry standards
+ Represent the team as the lead contact on projects
+ Lead or provide input on process improvements
**Keys to Success**
We are looking for an expert publication writer to join the team. The Senior Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from kick-off to completion. The successful candidate will have extensive experience in creating publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek a bright teammate who is proactive, enjoys challenges, and can thrive in a highly collaborative CRO (contract research organization) environment.
**Education, Experience & Skills**
+ Extensive proven experience as a writer of peer-reviewed medical publications
+ Experience working in a CRO environment preferred
+ Experience of generating publication extenders (e.g., plain language summaries, video/graphical abstracts) advantageous
+ Experience of publication planning/strategy advantageous
+ Excellent scientific writing, project management, and digital literacy
+ Bachelor's degree or higher in a scientific field; advanced degree preferred
+ In-depth knowledge of different therapeutic areas
+ Additional qualifications (e.g., EMWA or CMPP certification) advantageous
+ Sound professional judgement in dealing with inquiries, issues, and customer concerns
+ Able to independently make decisions and solve problems
+ Comfortable working on multiple projects concurrently
+ Able to prioritize and delegate tasks effectively
+ Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
**Physical Requirements / Work Environment**
+ Work will be 100% remote (home based)
+ Occasional domestic and international travel may be required
**Why Join Us?**
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Thermo Fisher Scientific does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other legally protected status.
**NOTE: Please include in your application a cover letter describing your qualifications for the role.**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Is this job a match or a miss?
Apply Now
1
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Effective communication of evidence and information is essential to conveying the value of products. With approximately 20 years of experience, our highly trained staff provide medical writing services for all phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standard processes, and your corporate guidance.
**IMPORTANT: a cover letter describing your qualifications is required, along with your resume to be considered.**
**Discover Impactful Work**
The Publications and Scientific Communications team, a part of Medical Writing and Healthcare Communications, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**A day in the life:**
· Write, edit, and handle publications and other scientific communications (manuscripts, posters, abstracts, oral presentation slide decks, and review articles), on time, within budget, and with little instruction. Provides senior review of documents.
· Appropriately resolve or raise project management issues, such as out-of-scope activities
· Ensure compliance with quality processes and requirements
· Represent the team as a prime contact on projects, establishes clients relationships.
· Assist in business development initiatives
· Lead or provide input on initiatives for process improvement, provides training and mentorship of other writers.
**Keys to Success:**
We are looking for an expert publications' writer to join the team. The Principal Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from conception to completion. The successful candidate will have extensive experience in writing publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek an excellent teammate who is proactive, enjoys challenges, can work on multiple projects concurrently, and is can work in a highly collaborative CRO environment.
**Education and Experience**
· Extensive proven experience as a writer of peer-reviewed medical publications (comparable to 8+ years); experience working in a CRO environment preferred
· Excellent scientific writing, project management, and digital literacy
· Bachelor's degree or higher in a scientific field; advanced degree preferred
· In-depth knowledge of relevant specialty areas of medicine
· Additional qualifications (AMWA, EMWA, or RAC training; CMPP certification) advantageous
· Excellent written English. Proactive communicator
· Sound professional judgement in dealing with inquiries, issues, and customer concerns; able to independently make decisions and solve problems
· Comfortable working on multiple projects concurrently
· Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Effective communication of evidence and information is essential to conveying the value of products. With approximately 20 years of experience, our highly trained staff provide medical writing services for all phases of the product lifecycle, helping to create a consistency in quality and voice. Our writers prepare documents that are clear, concise, compelling, and scientifically accurate, while also ensuring they are fully aligned with regulations, industry standard processes, and your corporate guidance.
**IMPORTANT: a cover letter describing your qualifications is required, along with your resume to be considered.**
**Discover Impactful Work**
The Publications and Scientific Communications team, a part of Medical Writing and Healthcare Communications, prepares medical publications, abstracts, posters, presentations, and other scientific communications. Our dynamic, highly collaborative team focuses on providing quality writing to internal collaborators and external pharmaceutical and biotech clients.
**A day in the life:**
· Write, edit, and handle publications and other scientific communications (manuscripts, posters, abstracts, oral presentation slide decks, and review articles), on time, within budget, and with little instruction. Provides senior review of documents.
· Appropriately resolve or raise project management issues, such as out-of-scope activities
· Ensure compliance with quality processes and requirements
· Represent the team as a prime contact on projects, establishes clients relationships.
· Assist in business development initiatives
· Lead or provide input on initiatives for process improvement, provides training and mentorship of other writers.
**Keys to Success:**
We are looking for an expert publications' writer to join the team. The Principal Medical Writer will be responsible for leading and producing high-quality publications and scientific communications, from conception to completion. The successful candidate will have extensive experience in writing publications, abstracts, and posters, as well as excellent written English and analytical skills. We seek an excellent teammate who is proactive, enjoys challenges, can work on multiple projects concurrently, and is can work in a highly collaborative CRO environment.
**Education and Experience**
· Extensive proven experience as a writer of peer-reviewed medical publications (comparable to 8+ years); experience working in a CRO environment preferred
· Excellent scientific writing, project management, and digital literacy
· Bachelor's degree or higher in a scientific field; advanced degree preferred
· In-depth knowledge of relevant specialty areas of medicine
· Additional qualifications (AMWA, EMWA, or RAC training; CMPP certification) advantageous
· Excellent written English. Proactive communicator
· Sound professional judgement in dealing with inquiries, issues, and customer concerns; able to independently make decisions and solve problems
· Comfortable working on multiple projects concurrently
· Able to complete work within fixed budgets and timelines and to facilitate conflict resolution among team members and clients
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today! Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Is this job a match or a miss?
Apply Now
2
Job Description
**Who we want**
**- Performance** : Deliver high quality products.
**- Team Player:** Build positive relationships with others to achieve common goals.
**- Reliable:** Manage time to effectively get the job done.
A Manufacturing Operator at Stryker performs the activities associated with the specific Standard Operation Procedures (SOPs) for the purpose of manufacturing, inspection or packaging of Medical Devices
**What you will do**
The Manufacturing Operator will be responsible for some or all of the below:
- Producing and/or packaging and labeling high quality product within a team environment,
in line with standard operating procedures.
- Inspecting components by using precision measuring equipment to ensure components
meet engineering specifications.
- Completing production records and maintenance logs.
- Maintaining a high standard of housekeeping
- Adhering to all Health and Safety procedures and requirements.
- Final Inspection Activities to include finished goods inspection and DHR review.
- Demonstrating safe working practices, correct use of equipment, product verification and
the adherence to EHS, line clearance and 5 pillars compliance.
**What you need**
- Leaving Certificate, Trade or equivalent education level is required.
- Experience in a regulated manufacturing machine environment is an advantage
- Capable of working as part of a multi-disciplined team
- Good Communication Skills
**Shift availability and schedule (days and times)**
**Morning shift 05:00am - 1pm (Mon-Thurs), 05:00am - 12pm on Fridays,**
**or**
**Evening shift 13:00pm - 21:00pm (Mon-Thurs), 12:00pm - 7pm on Fridays.**
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
**- Performance** : Deliver high quality products.
**- Team Player:** Build positive relationships with others to achieve common goals.
**- Reliable:** Manage time to effectively get the job done.
A Manufacturing Operator at Stryker performs the activities associated with the specific Standard Operation Procedures (SOPs) for the purpose of manufacturing, inspection or packaging of Medical Devices
**What you will do**
The Manufacturing Operator will be responsible for some or all of the below:
- Producing and/or packaging and labeling high quality product within a team environment,
in line with standard operating procedures.
- Inspecting components by using precision measuring equipment to ensure components
meet engineering specifications.
- Completing production records and maintenance logs.
- Maintaining a high standard of housekeeping
- Adhering to all Health and Safety procedures and requirements.
- Final Inspection Activities to include finished goods inspection and DHR review.
- Demonstrating safe working practices, correct use of equipment, product verification and
the adherence to EHS, line clearance and 5 pillars compliance.
**What you need**
- Leaving Certificate, Trade or equivalent education level is required.
- Experience in a regulated manufacturing machine environment is an advantage
- Capable of working as part of a multi-disciplined team
- Good Communication Skills
**Shift availability and schedule (days and times)**
**Morning shift 05:00am - 1pm (Mon-Thurs), 05:00am - 12pm on Fridays,**
**or**
**Evening shift 13:00pm - 21:00pm (Mon-Thurs), 12:00pm - 7pm on Fridays.**
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Is this job a match or a miss?
Apply Now
3
Job Description
**Join IQVIA on our mission to accelerate innovation for a healthier world!**
IQVIA UK's cFSP (sponsor-dedicated) team is seeking experienced Clinical Research Associates in Ireland.
**Why IQVIA?**
+ Career development opportunities to grow as we grow
+ AI‑powered career advancement through our internal talent marketplace, Career Connections
+ Flexible working to assist work-life balance and professional success
+ Well‑being support covering your physical, mental, and financial health
**Awards**
+ 2026 "Glassdoor Best Place to Work in the UK"
+ \#1 in category - 2026 Fortune® World's Most Admired Companies list (for the FIFTH consecutive year!)
+ Brandon Hall Excellence Award for Learning & Development
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Requirements**
+ Requires at least 2 years on-site monitoring experience of interventional studies
+ Degree in scientific discipline or health care or equivalent industry experience
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Ability to establish and maintain effective working relationships with coworkers and clients
**Please note:** this position is not eligible for visa sponsorship.
**Apply today and forge a career with greater purpose, make an impact, and never stop learning!**
\#LI-ADAMTHOMPSON
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
IQVIA UK's cFSP (sponsor-dedicated) team is seeking experienced Clinical Research Associates in Ireland.
**Why IQVIA?**
+ Career development opportunities to grow as we grow
+ AI‑powered career advancement through our internal talent marketplace, Career Connections
+ Flexible working to assist work-life balance and professional success
+ Well‑being support covering your physical, mental, and financial health
**Awards**
+ 2026 "Glassdoor Best Place to Work in the UK"
+ \#1 in category - 2026 Fortune® World's Most Admired Companies list (for the FIFTH consecutive year!)
+ Brandon Hall Excellence Award for Learning & Development
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Requirements**
+ Requires at least 2 years on-site monitoring experience of interventional studies
+ Degree in scientific discipline or health care or equivalent industry experience
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Ability to establish and maintain effective working relationships with coworkers and clients
**Please note:** this position is not eligible for visa sponsorship.
**Apply today and forge a career with greater purpose, make an impact, and never stop learning!**
\#LI-ADAMTHOMPSON
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Is this job a match or a miss?
Apply Now
4
Job Description
Job Description
**Shift - This role is for the Weekend shift. Working hours are 7am - 7pm, Friday, Saturday and Sunday.**
**Who we want**
+ **Performance** : Deliver high quality products.
+ **Team Player** : Build positive relationships with others to achieve common goals.
+ **Reliable** : Manage time to effectively get the job done.
A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
*** Please note this is initially a 12 month fixed term contract based in our Model Farm Road location**
\#IJ
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
**Shift - This role is for the Weekend shift. Working hours are 7am - 7pm, Friday, Saturday and Sunday.**
**Who we want**
+ **Performance** : Deliver high quality products.
+ **Team Player** : Build positive relationships with others to achieve common goals.
+ **Reliable** : Manage time to effectively get the job done.
A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
*** Please note this is initially a 12 month fixed term contract based in our Model Farm Road location**
\#IJ
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Is this job a match or a miss?
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5
Job Description
Company Description
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
AbbVie Westport is the largest operating facility in the AbbVie global network, the site is a dynamic, fast-paced environment with a strong pipeline of new product introductions, technology transfers, and development projects spanning both small and large molecule programs.
We are looking for a talented and driven Principal Research Scientist I to join our team, supporting the Small Molecule Business Units. This is an exciting opportunity to play a central role in bringing innovative ophthalmic products to patients worldwide, working within a highly collaborative team of scientific and technical professionals.
Purpose:
To lead research and project activities, as well as the professional development of a small group of scientists, within the area of expertise through effective mentoring, guidance, and supervision. This role will independently conceive, execute, and communicate innovative multidisciplinary research or development strategies that support project and functional goals, while serving as a lead scientist on their own project and contributing scientific insight across multiple other projects. In addition, the role will act as an effective people leader, fostering team development, engagement, and high performance.
Responsibilities:
+ Supervise a team of scientists. Evaluate the performance of those individuals; be accountable for the effective performance of the team/individuals. Foster individual development within the team.
+ Proactively contributes to the performance and growth of the wider analytical department. Promote integration within global PDS&T function.
+ Effectively function as a principle investigator/project manager, generating original technical ideas and research or development strategies.
+ Demonstrate creative 'out of the box' thinking to solve difficult problems and champion new technologies to achieve project goals.
+ Independently responsible for project science within his/her area of expertise on one or more project teams.
+ Make significant contributions to project team through lab based, or other work environments, activities.
+ Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies.
+ Recognized and sought out as an expert in his/her discipline within the company and possibly externally.
+ Primary author of publications, presentations, regulatory documents and/or primary inventor of patents. Present at leading scientific conferences.
Qualifications
-BSc or equivalent education and extensive, typically 14+ years of experience; MS or equivalent education with typically 12+ years of experience; PhD with typically 6+ years of experience in area or scientific area of discipline.
-Demonstrated ability to function as a principle investigator, generating original technical ideas and research or development strategies.
-Demonstrate creative 'out of the box' thinking to solve difficult technical problems and champion new technologies to achieve project goals.
-Recognized and sought out as an expert in his/her discipline within the company and possibly externally.
-Experienced and demonstrated success as primary author of publications, presentations, regulatory documents and/or primary inventor of patents.
-Demonstrated scientific communication and presentation skills by presenting at leading scientific conferences.
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:
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
AbbVie Westport is the largest operating facility in the AbbVie global network, the site is a dynamic, fast-paced environment with a strong pipeline of new product introductions, technology transfers, and development projects spanning both small and large molecule programs.
We are looking for a talented and driven Principal Research Scientist I to join our team, supporting the Small Molecule Business Units. This is an exciting opportunity to play a central role in bringing innovative ophthalmic products to patients worldwide, working within a highly collaborative team of scientific and technical professionals.
Purpose:
To lead research and project activities, as well as the professional development of a small group of scientists, within the area of expertise through effective mentoring, guidance, and supervision. This role will independently conceive, execute, and communicate innovative multidisciplinary research or development strategies that support project and functional goals, while serving as a lead scientist on their own project and contributing scientific insight across multiple other projects. In addition, the role will act as an effective people leader, fostering team development, engagement, and high performance.
Responsibilities:
+ Supervise a team of scientists. Evaluate the performance of those individuals; be accountable for the effective performance of the team/individuals. Foster individual development within the team.
+ Proactively contributes to the performance and growth of the wider analytical department. Promote integration within global PDS&T function.
+ Effectively function as a principle investigator/project manager, generating original technical ideas and research or development strategies.
+ Demonstrate creative 'out of the box' thinking to solve difficult problems and champion new technologies to achieve project goals.
+ Independently responsible for project science within his/her area of expertise on one or more project teams.
+ Make significant contributions to project team through lab based, or other work environments, activities.
+ Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies.
+ Recognized and sought out as an expert in his/her discipline within the company and possibly externally.
+ Primary author of publications, presentations, regulatory documents and/or primary inventor of patents. Present at leading scientific conferences.
Qualifications
-BSc or equivalent education and extensive, typically 14+ years of experience; MS or equivalent education with typically 12+ years of experience; PhD with typically 6+ years of experience in area or scientific area of discipline.
-Demonstrated ability to function as a principle investigator, generating original technical ideas and research or development strategies.
-Demonstrate creative 'out of the box' thinking to solve difficult technical problems and champion new technologies to achieve project goals.
-Recognized and sought out as an expert in his/her discipline within the company and possibly externally.
-Experienced and demonstrated success as primary author of publications, presentations, regulatory documents and/or primary inventor of patents.
-Demonstrated scientific communication and presentation skills by presenting at leading scientific conferences.
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:
Is this job a match or a miss?
Apply Now
6
Job Description
**We Are Teva**
We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
**The Opportunity**
We would like to invite applications for the role of Site Microbiologist at our Waterford site. This is a Permanent Position.
The Site Microbiologist is responsible for the Management of the Microbiology Lab and defines the microbiology strategy for the site in order to meet TEVA Waterford Operational and Quality objectives.
The successful person will be managing the full micro team for the site along with reviewing departmental performance and acting as the site main contact for all micro related queries.
There is no relocation support offered for this role.
**How You'll Spend Your Day**
+ Responsible for all micro queries and investigations around the site
+ Liaising with senior management on all queries relating to the micro team
+ Proactively plans for, develops and implement new projects and systems for the micro team on an ongoing basis
+ Being a subject matter expert on all matters relating to micro
+ Supports and drives the Contamination Control Strategy for the site in accordance with Annex 1 requirements
+ Develop and train the micro analysts on the team to the best standards
+ Deliver Customer Service (both internal and external) in accordance with Quality standards, 'TEVA Best Practices' and Cost Control.
+ Ensure that operational schedules are met with all batches being ready as needed
+ Ensure GMP compliant, cost effective systems are developed in place and operational in order to ensure all work carried out by Microbiology personnel is in compliance with required standards conforming to TEVA, cGMP, and Health and Safety, TEVA Best Practice and Environmental requirements.
+ Ensure the team are fully ready for all audits and inspections as required
**Your Skills and Experience**
**Are you:**
+ Third Level qualified in Microbiology (essential)
**Do you have:**
+ Extensive management experience in a high throughput Microbiology Laboratory within the Pharma industry
+ Excellent Knowledge of Regulatory USP/Ph.Eur/JP harmonised microbiological methods, method verification/development ensuring the site is in compliance with all micro regulations
+ Comprehensive Knowledge of Microbiology and Microbiological Techniques in the Pharma Industry
+ Knowledge of Steam Sterilisation and microbiological media.
+ Knowledge of environmental control, routine monitoring and method validation.
+ Understanding of microorganisms and bioburden/contamination control and the risk associated with non-sterile inhalation products.
+ Knowledge of PW systems and microbial control
+ Knowledge of microbial identification methods
+ Good understanding of Contamination Control Strategy and Annex 1 requirements
**Already Working @TEVA?**
Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:
+ Be a current employee of Teva
+ Meet the basic requirements for the job
+ Have received a rating not lower than "Successful" on their most recent performance review and must not currently be on a performance improvement plan
+ Apply to the posted requisition within the allotted time frame
+ Have been in their current position for a minimum tenure of twelve (12) months
Unless explicitly stated in the job description, no company sponsored work authorisation or relocation assistance should be assumed.
**Deadline for internal applications will close on Friday 8th May 2026** **\#TJ**
**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
We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
**The Opportunity**
We would like to invite applications for the role of Site Microbiologist at our Waterford site. This is a Permanent Position.
The Site Microbiologist is responsible for the Management of the Microbiology Lab and defines the microbiology strategy for the site in order to meet TEVA Waterford Operational and Quality objectives.
The successful person will be managing the full micro team for the site along with reviewing departmental performance and acting as the site main contact for all micro related queries.
There is no relocation support offered for this role.
**How You'll Spend Your Day**
+ Responsible for all micro queries and investigations around the site
+ Liaising with senior management on all queries relating to the micro team
+ Proactively plans for, develops and implement new projects and systems for the micro team on an ongoing basis
+ Being a subject matter expert on all matters relating to micro
+ Supports and drives the Contamination Control Strategy for the site in accordance with Annex 1 requirements
+ Develop and train the micro analysts on the team to the best standards
+ Deliver Customer Service (both internal and external) in accordance with Quality standards, 'TEVA Best Practices' and Cost Control.
+ Ensure that operational schedules are met with all batches being ready as needed
+ Ensure GMP compliant, cost effective systems are developed in place and operational in order to ensure all work carried out by Microbiology personnel is in compliance with required standards conforming to TEVA, cGMP, and Health and Safety, TEVA Best Practice and Environmental requirements.
+ Ensure the team are fully ready for all audits and inspections as required
**Your Skills and Experience**
**Are you:**
+ Third Level qualified in Microbiology (essential)
**Do you have:**
+ Extensive management experience in a high throughput Microbiology Laboratory within the Pharma industry
+ Excellent Knowledge of Regulatory USP/Ph.Eur/JP harmonised microbiological methods, method verification/development ensuring the site is in compliance with all micro regulations
+ Comprehensive Knowledge of Microbiology and Microbiological Techniques in the Pharma Industry
+ Knowledge of Steam Sterilisation and microbiological media.
+ Knowledge of environmental control, routine monitoring and method validation.
+ Understanding of microorganisms and bioburden/contamination control and the risk associated with non-sterile inhalation products.
+ Knowledge of PW systems and microbial control
+ Knowledge of microbial identification methods
+ Good understanding of Contamination Control Strategy and Annex 1 requirements
**Already Working @TEVA?**
Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:
+ Be a current employee of Teva
+ Meet the basic requirements for the job
+ Have received a rating not lower than "Successful" on their most recent performance review and must not currently be on a performance improvement plan
+ Apply to the posted requisition within the allotted time frame
+ Have been in their current position for a minimum tenure of twelve (12) months
Unless explicitly stated in the job description, no company sponsored work authorisation or relocation assistance should be assumed.
**Deadline for internal applications will close on Friday 8th May 2026** **\#TJ**
**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
Is this job a match or a miss?
Apply Now
7
Job Description
IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
**Clinical FSP Business**
IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.
Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.
Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are 'indication and molecule experts'. Additionally, IQVIA's FSP business works with the Sponsors SOP's, creating more continuity for both parties.
Our models offer excellent opportunities for experienced CRA's to expand their knowledge and skills.
**What we Offer:**
+ Excellent salary and benefits package
+ Car allowance
+ We invest in keeping our teams stable, so workload is consistent
+ We offer genuine career development opportunities for those who want to grow as part of the organisation
+ We give the chance to work on cutting edge medicines, right at the forefront of new medicine development
**Role Details:**
+ Working in partnership with a single-sponsor
+ Usually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
+ On site between 6 and 8 days per month, dependant on the sponsor
+ All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
+ Permanent employment contract
+ Fantastic work/life balance
+ Sponsor model has reduced travel (approx. 30% or less) due to using 'Fit for Purpose Monitoring' which incorporates remote monitoring therefore there is less need for on-site visits
**Responsibilities:**
+ Site management and monitoring activities across the country
+ Work with sites to adapt, drive and track subject recruitment plan
+ Provide protocol and study training to the assigned sites
+ Create and maintain monitoring visit reports and action plans
+ If appropriate, co-monitor, train and mentor junior members of the team
**Become part of our team.**
We believe in hiring the best talent in the industry.
**To become part of our team, you should:**
+ Have a degree in Life Sciences or have equivalent experience within a nursing background.
+ Have at least 12 months of independent on-site monitoring experience
+ Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
+ Have in depth GCP knowledge
+ Be flexible with the ability to travel nationwide
+ Hold a full driving license
+ Possess strong communication, written and presentation skills are a must (must have fluency in English)
+ Whatever your career goals, we are here to ensure you get there!
*Please note - this role is not eligible for VISA sponsorship*
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
**Clinical FSP Business**
IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.
Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.
Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are 'indication and molecule experts'. Additionally, IQVIA's FSP business works with the Sponsors SOP's, creating more continuity for both parties.
Our models offer excellent opportunities for experienced CRA's to expand their knowledge and skills.
**What we Offer:**
+ Excellent salary and benefits package
+ Car allowance
+ We invest in keeping our teams stable, so workload is consistent
+ We offer genuine career development opportunities for those who want to grow as part of the organisation
+ We give the chance to work on cutting edge medicines, right at the forefront of new medicine development
**Role Details:**
+ Working in partnership with a single-sponsor
+ Usually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
+ On site between 6 and 8 days per month, dependant on the sponsor
+ All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
+ Permanent employment contract
+ Fantastic work/life balance
+ Sponsor model has reduced travel (approx. 30% or less) due to using 'Fit for Purpose Monitoring' which incorporates remote monitoring therefore there is less need for on-site visits
**Responsibilities:**
+ Site management and monitoring activities across the country
+ Work with sites to adapt, drive and track subject recruitment plan
+ Provide protocol and study training to the assigned sites
+ Create and maintain monitoring visit reports and action plans
+ If appropriate, co-monitor, train and mentor junior members of the team
**Become part of our team.**
We believe in hiring the best talent in the industry.
**To become part of our team, you should:**
+ Have a degree in Life Sciences or have equivalent experience within a nursing background.
+ Have at least 12 months of independent on-site monitoring experience
+ Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
+ Have in depth GCP knowledge
+ Be flexible with the ability to travel nationwide
+ Hold a full driving license
+ Possess strong communication, written and presentation skills are a must (must have fluency in English)
+ Whatever your career goals, we are here to ensure you get there!
*Please note - this role is not eligible for VISA sponsorship*
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Is this job a match or a miss?
Apply Now
8
Job Description
Company Description
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 6 month fixed-term contract. This role is rotational shift work.
In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements.
A snapshot of your key responsibilities as a Pharmaceutical Technician would be:
+ Pharmaceutical processing activities in our manufacturing building and support locations.
+ Team co-ordination to maximise the effectiveness of the team members.
+ Documentation of all activities in line with cGMP requirements.
+ Cross training within the team and training of new team members.
+ Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
+ Execution of commissioning and validation protocols on an ongoing basis.
+ Maintaining the overall cGMP of the pharmaceutical processing areas.
+ Adheres to and supports all EHS & E standards, procedures, and policies.
Qualifications
+ 3rd level qualification, preferably in Engineering or Science related fields OR 2+ years in a GMP regulated environment.
+ Experience of operating in a highly automated environment.
+ Good I.T. skills are required.
Additional Information
This role operates on a 3 cycle shift.
Example:
Week One: Days
Week Two: Evenings
Week Three: Nights
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:
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 6 month fixed-term contract. This role is rotational shift work.
In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements.
A snapshot of your key responsibilities as a Pharmaceutical Technician would be:
+ Pharmaceutical processing activities in our manufacturing building and support locations.
+ Team co-ordination to maximise the effectiveness of the team members.
+ Documentation of all activities in line with cGMP requirements.
+ Cross training within the team and training of new team members.
+ Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems.
+ Execution of commissioning and validation protocols on an ongoing basis.
+ Maintaining the overall cGMP of the pharmaceutical processing areas.
+ Adheres to and supports all EHS & E standards, procedures, and policies.
Qualifications
+ 3rd level qualification, preferably in Engineering or Science related fields OR 2+ years in a GMP regulated environment.
+ Experience of operating in a highly automated environment.
+ Good I.T. skills are required.
Additional Information
This role operates on a 3 cycle shift.
Example:
Week One: Days
Week Two: Evenings
Week Three: Nights
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:
Is this job a match or a miss?
Apply Now
9