Similar posts
Regulatory Affairs Manager
- Permanent
- Consultant / Specialist
- United Kingdom
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a dedicated and detail-oriented individual for the role of Regulatory Affairs Manager. This role offers an exciting opportunity to manage a subteam within the Regulatory Department, providing exposure to various aspects of regulatory affairs from clinical trials to lifecycle management in medicines and medical devices.
Responsibilities:
- Oversee the submission, maintenance and control of regulatory information and documentation for medicines, medical devices, and other products.
- Ensure all submissions to regulatory authorities are of high quality and conducted in a professional and timely manner.
- Author and review technical documentation for alignment with applicable regulations and guidance.
- Act as signatory for appropriate medical device technical file sections and expert reports.
- Represent Regulatory Affairs as part of Research & Development (R&D) project teams and lead regulatory strategy discussions.
- Lead and support regulatory due diligence of new products.
- Manage workload of team for assigned projects in line with business priorities.
- Maintain oversight and responsibility for the artwork process and staff.
- Maintain awareness of existing and new legislation/guidance relating to EU, UK and RoW GxP; Medicines; Medical Devices and related ISO activities.
- Support and manage regulatory officers in the performance of their day-to-day activities.
Key Skills and Requirements:
- Degree or equivalent level within life sciences or chemistry.
- Experience in UK and EU pharmaceutical regulatory affairs.
- Experience of line management and/or leading a regulatory team.
- Good IT skills including MS Word, Excel and PowerPoint.
- Highly organized, with strong attention to detail.
- Strong problem-solving skills and ability to work independently.
- Strong communication skills, written and verbal.
If you are having difficulty in applying or if you have any questions, please contact Jaeme Pawl at j.pawl@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
Related jobs
Highly Competitive
Karlsruhe, Germany
Gestalten Sie die Zukunft medizinischer Innovationen - werden Sie Regulatory Affairs Specialist und übernehmen Sie die globale Compliance ab Karlsruhe!
US$220000.00 - US$265000 per annum + Highly Competitive Salary
Parsippany-Troy Hills, USA
We're hiring a senior regulatory leader to own clinical stage strategy across multiple programs.