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Sciences Manager jobs in Bridgewater, NJ

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Manager, Regulatory Affairs-CMC
Bridgewater, NJ
Overview **MEMBERS ONLY**SIGN UP NOW***, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance.  Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard ..

Last verified - 1 day(s) 15 hour(s) ago



Manager, Regulatory Affairs-CMC
Bridgewater, NJ
Overview Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance.  Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard ..

Last verified - 1 day(s) 12 hour(s) ago



Sales Operations Manager
Bridgewater, NJ
Overview The Manager, Sales Operations is responsible for management, oversight and delivery of all Sales Operations activities for the B L Pharma & WHC Business Units.  The Manager has a key role in managing the relationship and is the primary operations contact for various defined Specialty Pharma and Field Sales Teams as it ..

Last verified - 1 day(s) 12 hour(s) ago



Sr. Manager, Regulatory Affairs-Surgical
Bridgewater, NJ
Overview The Surgical Regulatory Affairs Sr Manager handles all regulatory development aspects of surgical devices. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due ..

Last verified - 1 day(s) 15 hour(s) ago



Sr. Manager, Regulatory Affairs (CMC)
Bridgewater, NJ
Overview The Regulatory Affairs \u2013 CMC Associate Director independently manages all regulatory CMC aspects of Valeant\u2019s Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Associate Director is responsible for the regulatory CMC strategies of all submissions for products under his/her responsibility as well as ..

Last verified - 1 day(s) 12 hour(s) ago


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Manager, Global Pharmacovigilance & Risk Mgmt (Aggregate Reporting)
Bridgewater, NJ
Overview - Preparation, distribution, and quality review of Aggregate reports- Oversight of vendor(s) for aggregate reports writing- Submission of Aggregate reports in collaboration with Regulatory Affairs- Provide training on aggregate reports or for other departments on pharmacovigilance related aspects- Provide coordination and support for the internal Pharmacovigilance activities within **MEMBERS ONLY**SIGN UP NOW***- ..

Last verified - 1 day(s) 15 hour(s) ago



Clinical Trial Manager
Bridgewater, NJ
SUMMARY: The Clinical Trial Manager is responsible for the overall management and oversight of phase I-IV clinical trials from start up through CSR, including but not limited to: development of project documentation, training project staff, monitoring study progress, assessing protocol adherence, administration and oversight of study budgets, management of third-party vendors ..

Last verified - 1 day(s) 7 hour(s) ago



Manager/Sr. Manager/Associate Director Regulatory Affairs CMC
Bridgewater, NJ
Overview The Regulatory Affairs \u2013 CMC Associate Director independently manages all regulatory CMC aspects of Valeant\u2019s Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Associate Director is responsible for the regulatory CMC strategies of all submissions for products under his/her responsibility as well as ..

Last verified - 1 day(s) 15 hour(s) ago



Sr. Manager, Regulatory Affairs-Surgical
Bridgewater, NJ
Overview The Surgical Regulatory Affairs Sr Manager handles all regulatory development aspects of surgical devices. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due ..

Last verified - 1 day(s) 12 hour(s) ago



Sr. Manager, Regulatory Affairs (CMC)
Bridgewater, NJ
Overview The Regulatory Affairs \u2013 CMC Associate Director independently manages all regulatory CMC aspects of Valeant\u2019s Pharmaceuticals products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Associate Director is responsible for the regulatory CMC strategies of all submissions for products under his/her responsibility as well as ..

Last verified - 1 day(s) 15 hour(s) ago


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