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Exceptional opportunity - Senior Regulatory CMC Manager

This job is no longer available

Employer
SEC Recruitment
Posted
Friday, August 17, 2012
Closes
Sunday, September 16, 2012
Ref
ND0041.1307.sbn
Contact
Nikolay Dimitrov
Location
Switzerland
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Salary
Salary + Excellent relocation package + Benefits

Further information

Senior Regulatory CMC Manager, Small Molecules - Switzerland

My client, a large pharmaceutical company is looking for a Senior Regulatory CMC Manager to join the Regulatory CMC team in one of their sites located in Switzerland. To find out more about the role and company please call Nikolay on +41 (0)44 580 3717 / +49 (0)69 222 22 888 or send your CV to Nikolay.dimitrov@secpharma.com

As a Senior Regulatory CMC Manager you will provide strategic and operational global CMC regulatory direction for assigned projects through development, registration and life cycle management of chemical medicinal products (small molecules).

Responsibilities:
-Formulate, lead and drive global CMC regulatory strategy for assigned development projects and/or marketed products
-Proactively communicate CMC regulatory strategy to interdisciplinary project teams and to appropriate management level
-Lead and implement all global CMC submission activities while applying the global strategy into submissions
-Author high-quality CMC documentation for Health Authority submission
-Single point of contact with internal and external partners for all communication on development and/or marketed products
-Initiate and lead Health Authority interactions and negotiations
-Lead cross-functional Health Authority Response Teams
-Represent Reg CMC in interdisciplinary regulatory and technical project teams
-Act as a mentor/coach to all members of the RegCMC team.

Minimum Requirements:
-Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology, Cell Biology). PhD is preferred!
-4-6 years in Regulatory Affairs preferred, and experience in small molecules
-Working knowledge/experience in regulatory submission and approval processes for New Chemical Entities (NCE) and product life cycle management
-Proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements
-Proven track record of successfully working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects
-Demonstrated ability for strategic thinking, maintaining awareness of business impact
-Demonstrated ability for risk assessment and mitigation
-Strong interpersonal, communication, negotiation and problem solving skills
-Fluent English required (oral & written)

Nikolay Dimitrov
Pharmaceutical Division
Tel:
+44 (0)20 7255 6665
+33 (0)170807489
+49 (0)69 222 22 888
+41 (0)44 580 3717

Email: Nikolay.Dimitrov@secpharma.com
Web: www.secrecruitment.com


(Regulatory affairs, regulatory affairs manager, regulatory affairs, regulatory affairs, regulatory affairs, regulatory affairs manager)

SEC Recruitment

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