Regulatory / Regulatory Affairs Associate Director Global CMC - M4 Corridor

Reference: TM240120C

Expiry Date: 24-12-2020

Category Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
Maidenhead
Windsor and Maidenhead
United Kingdom

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Job Description

Regulatory / Regulatory Affairs Associate Director Global CMC - M4 Corridor

“Due to further planned expansion my client is seeking an Associate Director Regulatory CMC GRL for a for an exciting brand/portfolio leadership role with matrix reporting based in the South-East, M4 Corridor.”

My client is a global SME pharmaceutical company with a strong development pipeline and a number of Blockbuster marketed products.  Although considered medium in size, their spend on R&D make them competitive at the highest level and sales have continued to rise and rise year on year. With 5 major product launches planned over the next 3-4 years they are hitting impressive levels of growth and achievement.

For Regulatory Affairs CMC, they offer roles at EU and Global levels from their global head office based in the South-East/M4 Corridor and have gained a great reputation for giving regulatory professionals real career progression including direct people management.

The Role:

This is a global regulatory CMC leadership role (covering EU, US, LatAm, MENA, AP, EEU) where you will be responsible for a successful Brand/Portfolio including marketed products and late phase development candidates (small molecules). You will be leading and co-ordinating CMC regulatory and related change control activities for these projects and matrix leading EU and US RA CMC liaisons on Regulatory Sub Teams, Global CMC Development Teams and Regulatory/QA liaison team for marketed products advising on Regulatory CMC issues. The US offices are also on the East Coast, and with the Global HQ in Europe there are no late-evening US calls.

Experience need:

Ideally you will offer extensive CMC regulatory project management and leadership experience, having working closely with manufacturing sites, R&D and regional regulatory colleagues, with an enthusiastic, positive, and proactive approach, with a determination to succeed. You will have at least 10 years in Regulatory Affairs CMC and have experience of European & International CMC regulatory submissions, requirements and procedures.

Remuneration:

The package on offer is excellent and includes a full and comprehensive benefits package with full medical coverage for you and your family. The salary, bonus and car allowance are very competitive and you will receive a yearly stock options package. There is great flexibility around home working and time spent in the office, which offers a very nice work-life balance. 

Location:

Based in the M4 Corridor, my client is easily commutable from Maidenhead, Slough, High Wycombe, West London and Oxford. Parking is available.

To Apply!

To apply for this role, please press the red “Apply for position” button, or contact Theo Moore on +44 (0)207 801 3384 or Oli Dimitrov on +44 (0)207 801 3388 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.

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