Associate Director, Analytical Development- CA The position is responsible for managing contract partners in their analytical method development, method validation, release testing, and stability testing of APIs and drug products for all of the company's global development programs, from first-in-man to commercial registration. This role will also support of drug development from Phase 1 to commercialization. The incumbent will also be accountable for overseeing the scientific rigor and quality of analytical work by contract partners as well as a member of the CMC teams and report to the Program Director of Analytical Development.
Director, Regulatory Affairs- PA 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- NJ Our 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.
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. Manager, Associate Director Medical Affairs- MA 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.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 50 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.
Also currently recruiting for:
Sr. Scientist, Analytical Development- Late Phase Development- NJ
Sr. Research Associate, Analytical R&D-CA
Principal Scientist, Formulation Development- OSD-NJ
Sr. Regulatory Affairs Specialist- NDA- PA
Sr. Regulatory Affairs Specialist- ANDA-PA
Director, Regulatory Affairs- PA 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- NJ Our 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.
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. Manager, Associate Director Medical Affairs- MA 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.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 50 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.
Also currently recruiting for:
Sr. Scientist, Analytical Development- Late Phase Development- NJ
Sr. Research Associate, Analytical R&D-CA
Principal Scientist, Formulation Development- OSD-NJ
Sr. Regulatory Affairs Specialist- NDA- PA
Sr. Regulatory Affairs Specialist- ANDA-PA
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Copyright 2017-2019