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Regulatory Affairs Jobs

1 - 15 of 157
1 - 15 of 157
Search Results - Regulatory Affairs Jobs
Cregg-Galway
Senior Regulatory Affairs Specialist Excellent opportunity for a Senior Regulatory Affairs Specialist to join a thriving company in Co. Galway. The Senior Regulatory Affairs Specialist will be responsible for all aspects of regulatory in the region...
Force Recruitment Formerly Pharmaforce Limited-Galway
Role Title: Senior Regulatory Affairs Specialist II (Strategic Regulatory) Role Type: Permanent We are currently recruiting a Senior Regulatory Affairs Specialist II for a Medical Device Manufacturer in Co. Galway. A regulatory strategy involves...
South East Technological University-Carlow
Vacancy ID :  •  040344 Closing Date : 15 -May-2026 12:00 Vacancy: 040344  •  Pro Rata Part Time Assistant Lecturer  •  Pharmaceutical Regulatory Affairs Contract: Fixed Term  •  2 years Salary: Assistant Lecturer salary scale: €47,101  •  €63,735 (Pro rata...
CREGG-Dublin
Senior Regulatory Affairs Specialist – EMEA Region The Senior Regulatory Affairs Specialist for EMEA region will be responsible for all aspects of regulatory in the region, including but not limited to: ingredient review, marketing collateral...
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South East Technological University-Carlow
Vacancy ID :  •  040344 Closing Date : 15 -May-2026 12:00 Vacancy: 040344  •  Pro Rata Part Time Assistant Lecturer  •  Pharmaceutical Regulatory Affairs Contract: Fixed Term  •  2 years Salary: Assistant Lecturer salary scale: €47,101  •  €63,735 (Pro rata...
Force Recruitment Formerly Pharmaforce Limited-Galway
Role Title: Senior Regulatory Affairs Specialist II (Strategic Regulatory) Role Type: Permanent We are currently recruiting a Senior Regulatory Affairs Specialist II for a Medical Device Manufacturer in Co. Galway. A regulatory strategy involves...
Collins McNicholas Recruitment-Galway
A leading recruitment company is seeking a Regulatory Affairs IVDR Specialist to join their Galway team on a 6-month contract. Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap. The role involves...
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Sigmar Recruitment-Galway
Senior Regulatory Affairs Specialist About Your New Employer Join an innovative international company dedicated to quality and compliance across the EMEA region. Work in a dynamic environment with exposure to medical devices, wellness products...
Truly-Dublin
A medical device manufacturing company in Dublin is seeking a Regulatory Affairs Manager to build and lead the regulatory and quality functions. Ensure all your application information is up to date and in order before applying for this opportunity...
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Collins McNicholas Recruitment-Galway
that works under limited supervision.  •  Applies subject matter knowledge in the area of Regulatory Affairs.  •  Requires capacity to apply skills/knowledge within the context of specific needs or requirements. MAIN RESPONSIBILITIES  •  As the Experienced...
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Life Science Recruitment-Ireland
Regulatory Affairs Manager – Medical Devices Remember to check your CV before applying Also, ensure you read through all the requirements related to this role. We are supporting a growing medical device manufacturer in the appointment...
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CPL-Galway
Director of Regulatory Affairs – Global NPD Athenry, Co. Galway | Permanent | Onsite to start following Hybrid flexibility post probationary period. We’re partnering with a high‑growth global wellness company to appoint a Director of Regulatory...
cpl.com -
Collins McNicholas Recruitment-Galway
A leading recruitment company is seeking a Regulatory Affairs IVDR Specialist to join their Galway team on a 6-month contract. The role involves directing product registration submissions, interacting with regulatory agencies for approvals...
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CareerWise Recruitment-Waterford
Regulatory Affairs Officer Our client who is a leading pharmaceutical company baesd in Waterford is looking for a Regulatory Affairs Specialist for a 9-month contract. If you have experience in regulatory affairs in the pharmaceutical...
Collins McNicholas Recruitment-Galway
on a 6 month contract | Fully onsite MAIN PURPOSE OF ROLE  •  - Experienced professional individual contributor that works under limited supervision.  •  Applies subject matter knowledge in the area of Regulatory Affairs.  •  Requires capacity to apply...
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