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Search Results for Medical Affairs
Job Title. Location Salary Actions

Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist Job purpose: The Sr. Regulatory Affairs Specialist will develop strategies for complex projects and issues related to regulatory processes, compliance activities, documents, submissions, investigations, product development planning and regulatory agency interaction. The Sr. Regulatory position will assist in mentoring and development of staff members as part of the role. Key responsibilities: • Key responsibilities will include (but are not limited to) the following: • Support global regulatory projects,...

Location: Westmeath,
Senior Regulatory Affairs Specialist
Westmeath Not Disclosed

Regulatory Affairs Specialist - CN001

Regulatory Affairs Specialist Summary Our client is a large Medical Device organisation based in Athlone. They wish to recruit a Regulatory Affairs Specialist who will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for medical products globally Key responsibilites • Apply technical solutions to problem solving • Apply technical solutions to quality improvement projects • Use technical writing skills to clearly describe technical information • Analyze custo...

Location: Westmeath,
Regulatory Affairs Specialist - CN001
Westmeath Not Disclosed

Regulatory Affairs Manager

Regulatory Affairs Manager Our client is an international pharmaceutical discovery organisation and they are currently recruiting for a Regulatory Affairs Manager to join their team on a permanent basis. The ideal candidate will be a dynamic individual, who is self-driven, organized and capable of working on their own initiative in a start-up environment. Responsibilities • Coordinate, prepare and be accountable for all regulatory affairs related activities such as clinical trial applications, organization and preparation of regulatory advice meetings and compilation...

Location: Dublin,
Regulatory Affairs Manager
Dublin Not Disclosed

Senior Director, Regulatory Affairs

Our client is a Biopharma organization from the US with office based in Dublin in the last year. They are seeking a Senior Director of their Regulatory Affairs. The incumbent will be responsible for leading the Regulatory Affairs functions within Europe and specific additional regions. A scientific degree with a minimum of 5 years Regulatory experience (10 years Pharmaceutical experience) is required as a minimum. 20% travel associated with this role. Role/Responsibilities: • Ensure appropriate support for program maintenance, post-marketing studies and development ...

Location: Dublin,
Senior Director, Regulatory Affairs
Dublin Not Disclosed

CMC Regulatory Affairs Director

Our client is a Biopharma organisation with offices in Dublin. They are currently seeking a Director, CMC Regulatory Affairs, who will be responsible for providing tactical and strategic regulatory support for marketed products and development programs. A degree in Science with at least 8 years relevant CMC Regulatory experience is essential. Role/Responsibilities: • As part of his/her responsibilities, the Director will collaborate with key functional areas (including Technical Operations and Quality) to prepare high quality, timely, and effective regulatory...

Location: Dublin,
CMC Regulatory Affairs Director
Dublin Not Disclosed

Senior CMC Reg Affairs Specialist

Senior CMC Reg Affairs Specialist Our client is an organisation with a focus on the development and manufacture of generic pharmaceutical products. They are currently recruiting for a Senior CMC Reg Affairs Specialist to join their team based in Dublin. The successful candidate will report directly to the Head of Regulatory Affairs. The role will include some travel. Responsibilities • Critical review of high quality, Chemistry Manufacturing and Control (CMC) detailed regulatory documents and identify any possible deficiencies prior to dossier submission to EU and US A...

Location: Dublin,
Senior CMC Reg Affairs Specialist
Dublin Not Disclosed

QA Senior Associate (Contract)

Plant QA Snr Associate Level 4 Dun Laoghaire Overview: The Plant Quality Assurance (PQA) Snr Associate will typically report to a QA Senior Manager and is a core member of the site Quality Assurance team. The PQA Snr Associate will serve as Quality point of contact for manufacturing operations. The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, PQA Snr Associates may be asked to carry out additional work functions to support site continuous improvement activities. A...

Location: Dublin,
QA Senior Associate (Contract)
Dublin Not Disclosed

Head of Quality & Regulatory Affairs

Head of Quality & Regulatory Affairs Our client a multinational healthcare company currently seeks Head of Quality and Regulatory Affairs. Reporting to Ge

Location: Dublin,
Head of Quality & Regulatory Affairs
Dublin Not Disclosed