Senior Manager Regulatory Affairs

JR United Kingdom; Stockport; On-site; GBP 50,000 - 75,000; Full time

Job summary

A leading pharmaceutical company is seeking a Senior Manager Regulatory Affairs for a 12-month contract in Stockport. This strategic role involves shaping regional regulatory strategy, leading submissions, and ensuring compliance. The ideal candidate will have a degree and over five years of relevant experience.

Qualifications

• Degree required, preferably in a relevant field.
• 5+ years of relevant experience in regulatory affairs.

Responsibilities

• Shape and implement regional regulatory strategy, ensuring compliance with local regulations.
• Lead regulatory submissions, ensuring successful engagement with health authorities.
• Monitor and interpret evolving regional regulations for product development.

Education

Degree

Job description

Senior Manager Regulatory Affairs, stockport

Client:

Planet Pharma

Location:

stockport, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

3

Posted:

31.05.2025

Expiry Date:

15.07.2025

Job Description:

Planet Pharma are partnered with a leading pharmaceutical company and we are actively seeking an experienced Senior Manager Regulatory Affairs to join the business on an initial 12 month contract basis.

Key Responsibilities:

• Shape and implement regional regulatory strategy by advising the Global Regulatory Team (GRT), ensuring regional requirements are fully integrated and aligned with global development goals.
• Lead regulatory submissions and agency interactions across clinical trial and marketing applications, ensuring compliance with local regulations and successful engagement with health authorities.
• Drive development of product labeling and regulatory documentation, negotiating with regional agencies and collaborating with global teams to align on commercial and scientific objectives.
• Monitor and interpret evolving regional regulations, providing strategic insights and risk assessments to support product development, compliance, and regulatory success.

Key Requirements:

• Degree
• 5+ years relevant experience

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com

Please click ‘apply’ or contact Harry Banks (Recruiter II) at Planet Pharma for more information:

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.

Bank or payment details should not be provided when applying for a job. Eurojobs.com is not responsible for any external website content. All applications should be made via the 'Apply now' button.

Created on 31/05/2025 by JR United Kingdom