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Senior Regulatory affairs specialist/Manager CMC

Michael Bailey Associates - Zurich

Posted on Aug 18, 2021 by Michael Bailey Associates - Zurich

Basel, Switzerland
1 Sep 2021
Annual Salary

New opportunity has been created for a Senior Regulatory Affairs Specialist/manager CMC in the global pharmaceutical company with HQ based in Basel. This is 12 months contract role with possibility of extension.

Major Activities
1. Authoring 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 life cycle.
2. Prepare CMC responses to health authority questions during development, registration and product life cycle.
3. Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.
4. 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.
5. Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.
6. Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.
7. Establish and maintain sound working relationships with partners and customers.
8. Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).

* Degree in Science (eg Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent
* 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 for small molecules
* 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.

Please send your CV

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

Reference: 1291058161

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