Sr. Manager, Associate Director Medical Affairs- Associate Director, Medical Affairs is responsible for the development and management of the clinical affairs function through in the support of the companies Interventional Surgery product development and overall business objectives. The Associate Director assures compliance with applicable regulations regarding all pre-market and post-market product clinical study activities as defined within company procedures. He/she will provide strategic direction for clinical evaluation of products in support of regulatory approval and marketing needs. This individual is subject-matter expert in clinical affairs management and execution.
Director, Regulatory Affairs-MA- The Director of Regulatory Affairs is responsible for developing and managing the regulatory strategy for current and future self-assembling material-based products to ensure the timely preparation of organized and scientifically valid regulatory submissions in various geographic jurisdictions. This individual is also responsible for all regulatory maintenance activities, including periodic reporting requirements for this class III device
Sr. SCIENTIST, ANALYTICAL R&D- CA- My client is a top 20 Global Pharmaceutical corporation. They are looking to hire a Principal Scientist to lead a team of chemists. Must have strong method development and validation experience preferably working with NCE's.
Sr. Research Associate CA- Specialty Pharmaceutical company looking for a Sr Research Associate Analytical R&D. Must be able to independently develop and validate analytical methods specifically working with small molecules. Must also be able to perform methods development and validation for in-process and final product analyses.
QA Manager CA- To ensure all operations are in full compliance with established Standard Test Methods, compendial methods, vendor methods and safety guidelines. Collaborate with QA and Supply Operations to forecast incoming raw materials that require testing. Incumbent must also manage both the raw material and reference standard programs including driving change controls and document change revisions for updates to specification documents as needed.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 20 Global Pharmaceutical corporation looking to hire a Sr. Principal Scientist to lead a team of scientists. Must have strong method development and validation experience preferably working with NCE's. Ph.D 8-10 years industry experience or MS 10-12 years of experience.
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Director, Regulatory Affairs-MA- The Director of Regulatory Affairs is responsible for developing and managing the regulatory strategy for current and future self-assembling material-based products to ensure the timely preparation of organized and scientifically valid regulatory submissions in various geographic jurisdictions. This individual is also responsible for all regulatory maintenance activities, including periodic reporting requirements for this class III device
Sr. SCIENTIST, ANALYTICAL R&D- CA- My client is a top 20 Global Pharmaceutical corporation. They are looking to hire a Principal Scientist to lead a team of chemists. Must have strong method development and validation experience preferably working with NCE's.
Sr. Research Associate CA- Specialty Pharmaceutical company looking for a Sr Research Associate Analytical R&D. Must be able to independently develop and validate analytical methods specifically working with small molecules. Must also be able to perform methods development and validation for in-process and final product analyses.
QA Manager CA- To ensure all operations are in full compliance with established Standard Test Methods, compendial methods, vendor methods and safety guidelines. Collaborate with QA and Supply Operations to forecast incoming raw materials that require testing. Incumbent must also manage both the raw material and reference standard programs including driving change controls and document change revisions for updates to specification documents as needed.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 20 Global Pharmaceutical corporation looking to hire a Sr. Principal Scientist to lead a team of scientists. Must have strong method development and validation experience preferably working with NCE's. Ph.D 8-10 years industry experience or MS 10-12 years of experience.
Other notable roles currently recruiting for:
Sr. Regulatory Affairs Specialist-PA, NDA
Sr. Regulatory Affairs Specialist-PA, ANDA
Principal Scientist, Formulation Development, MN OSD
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