Regulatory Affairs Specialist -CMC

Sector:
Pharmaceutical
Location:
Switzerland
Sub-location:
Any
Currency:
CHF
Job Type:
Any
Salary Description:
excellent
Posted:
13/06/2019
Ref No:
122182

Major Activities:
Author CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle.
Prepare CMC responses to health authority questions during development, registration and product lifecycle.
Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
Identify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible.
Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.
Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.
Establish and maintain sound working relationships with partners and customers.
Assume activities in support of the general department such as annual and product renewal writing coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).


Ideal Background

Education:
Minimum: Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
Desirable: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent.

Experience/Professional requirement:

Regulatory experience in drug/biopharmaceutical products
Working knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines.
Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable.
Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload.
Effective planning, organizational and interpersonal skills.

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

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