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Senior Director CMC Regulatory Affairs - Hampshire

Business Type: Pharmaceutical Company
Job Type: Regulatory Affairs
Job Level: Not Specified
Position: Full Time
Salary: Competitive
Location: South East
Reference: 17762/001
Closing Date: 09/07/12
Our client is a leading global biopharmaceutical company. They are seeking a Senior CMC Regulatory Affairs Director for their offices in the South East
The Senior Director will be responsible for driving and ensuring a coordinated strategic global approach to CMC throughout all phases of development and registration (pre-IND to market support). Part of this role will include responsibility for the potential in-licensing assets as part of the business development process and for all regulatory agency interactions on CMC aspects, globally.

Leading, building, motivating and develop a team of CMC regulators
Ensuring a global coordinated consistent approach to CMC for all products at all phases of development and registration
Leading the regulatory aspects related to chemistry, manufacturing and controls, for new and existing products/projects
Ensuring the development of robust, global CMC strategies to ensure identification of key issues. Leads the development of risk assessment and mitigation plans
Providing regulatory senior leadership to the CMC regulators, setting a clear vision

M.Sc / Ph.D.
Solid Experience in regulatory CMC
Proven experience of leading a team at senior level and working and influencing remotely
Ideally a balance of experience in development and commercial CMC regulatory activities in the US, EU and other key markets
Excellent communications skills
Availability to travel internationally
BENEFITS: This company is seeking talented, motivated and team oriented individuals who are keen to make a difference. They offer highly competitive salaries and comprehensive benefits which include: pension, health, company relocation, stock options on joining, and annual bonus.

Fforde is acting as a recruitment agency/business.

To apply please email your CV to: or speak to our specialist consultant, Nicky Quinn on +44 (0)20 3627 8305. Visit our website and see all our job opportunities at
KEY WORDS: Regulatory Affairs, Director, Strategy, CMC, Regulatory, Drug Development, Drug Safety, Chemistry, Project Development, Project Management, Pharmaceutical, CRO, UK

Posted: 11/06/2012 | NPJ Ref: 83029
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