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May 25, 2018

Qa Supervisor


MSD PHARMACEUTICALS

... Quality Assurance. Demonstrated knowledge and understanding of current regulatory requirements for manufacture of licensed medicinal products. Problem solving and good communication skills. Technical report writing and database management. Knowledge of pharmaceutical manufacturing processes desirable. Responsibilities : Supports manufacturing operations on Quality issues. Responsible for reviewing technical and quality documents including: ...
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May 25, 2018

Medical Director


MSD PHARMACEUTICALS

... ensuring that functional groups (global clinical trial operations, regulatory affairs, pharmacovigilance and medical affairs) are collaboratively planning, ... the DPOC system. Building and managing relationships with regulatory and reimbursement authorities. Developing clinical trial strategy for ... ensuring that functional groups (global clinical trial operations, regulatory affairs, pharmacovigilance and medical affairs) are collaboratively planning, ...
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