Jobs: drug regulatory associate

K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. Seeking a Principal Regulatory Affairs Specialistto support the Kindeva business in maintaining regulatory compliance of existing manufactured products for customers on a global...

19901 Nordhoff St, Northridge, CA 91324, USA Job Description Posted Tuesday, March 19, 2024 at 4:00 AM K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world....

19901 Nordhoff St, Northridge, CA 91324, USA Job Description Posted Thursday, April 4, 2024 at 4:00 AM K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world....

19901 Nordhoff St, Northridge, CA 91324, USA Job Description Posted Thursday, April 4, 2024 at 4:00 AM K indeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world....

Summary This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory agencies...

Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...

Job DescriptionJob DescriptionSummaryThis position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams to prepare, review and submit regulatory filing documents, manage documentation systems and maintain...

Associate Director, Regulatory AffairsThis position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associates and Senior Regulatory Associates managing,...

Associate Director, Regulatory Affairs This position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associates and Senior Regulatory Associates...

Our client is a clinical stage biopharmaceutical company dedicated to improving patients lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms. Title: Associate Director, Formulation and Drug Delivery Location: South San Francisco, California Salary: $175k - 215k Position Summary: We are seeking an experienced and...

Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and through strategic partnerships with manufactures from around the world.JOB SUMMARY:The Senior Associate, Regulatory Affairs is responsible for supporting...

Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the groups own R&D facilities and through strategic partnerships with manufactures from around the world. JOB SUMMARY: The Senior Associate, Regulatory Affairs is responsible for supporting...

Job DescriptionJob DescriptionBreckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and through strategic partnerships with manufactures from around the world.JOB SUMMARY:The Senior Associate, Regulatory Affairs is...

Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the group’s own R&D facilities and through strategic partnerships with manufactures from around the world.JOB SUMMARY:The Senior Associate, Regulatory Affairs is responsible for supporting...

Our client is a clinical stage biopharmaceutical company dedicated to improving patients’ lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms.Title: Associate Director, Formulation and Drug DeliveryLocation: South San Francisco, California Salary: $175k - 215kPosition Summary:We are seeking an experienced and...

Our client is a clinical stage biopharmaceutical company dedicated to improving patients’ lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms.Title: Associate Director, Formulation and Drug DeliveryLocation: South San Francisco, California Salary: $175k - 215kPosition Summary:We are seeking an experienced and...

Our client is a clinical stage biopharmaceutical company dedicated to improving patients’ lives. They develop multiple precision medicines targeting hallmark cancer resistance mechanisms.Title: Associate Director, Formulation and Drug DeliveryLocation: South San Francisco, California Salary: $175k - 215kPosition Summary:We are seeking an experienced and...

Associate Director, Regulatory Affairs - Boston, MA - PermanentProclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA. Primary Responsibilities:The primary focus of this role is to work with internal and external stakeholders to ensure the timely release of finished products and...

Overview Celldex is a high growth clinical-stage biotechnology company focused on the development of immunotherapies for the treatment of inflammatory diseases and cancer. Celldex has validated pipeline programs, an experienced management team who pioneered early antibody technologies, and support from leading healthcare investors. At Celldex, you’ll work...

The International Regulatory Lead (Sr. Associate) is assigned to one or more Amgen products and may support an IRL or lead a program under the supervision of an experienced regulatory lead.Execute the international regulatory strategy and regulatory plans.Prepare supportive documentation for regulatory deliverables.Support regulatory product compliance (e.g....