Regulatory Affairs Associate: salario promedio en San Jose, CA in 2024

Prepare and coordinate the compilation and/or submission of documents to regulatory agencies in supp. ...

A Bachelor’s degree in a scientific field, preferably Chemistry or Pharmacy, with 1-3 years of experience, or a Master’s Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regul...

Regulatory Affairs Associate I. A Master's Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. Coordinate and track workflows for regulatory submissions. ...

Bachelor’s degree in a scientific field (Chemistry or Pharmacy preferred) with 1-3 years of experience, or a Master’s degree in Regulatory Affairs with a minimum of 3 months of internship experience. Prepare and coordinate regulatory submissions, including amendments, supplements, annual reports, an...

The Associate Regulatory Affairs Manager will be responsible for completing the regulatory work for the Health and Biosciences business and applicable joint ventures, with a focus on food applications, for the U. The The Associate Regulatory Affairs Manager is responsible for regulatory document dev...

The Associate Regulatory Affairs Manager will be responsible for completing the regulatory work for the Health and Biosciences business and applicable joint ventures, with a focus on food applications, for the U. Associate Regulatory Affairs Manager. Update Registration List to communicate the statu...

The Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Must have an extensive knowledge of regulatory requirements, including ICH and regional requirements, and have an understanding o...

The Associate Regulatory Affairs Manager will be responsible for completing the regulatory work for the Health and Biosciences business and applicable joint ventures, with a focus on food applications, for the U. The The Associate Regulatory Affairs Manager is responsible for regulatory document dev...

The Associate Regulatory Affairs Manager will be responsible for completing the regulatory work for the Health and Biosciences business and applicable joint ventures, with a focus on food applications, for the U. The Associate Regulatory Affairs Manager is responsible for regulatory document develop...

Regulatory Affairs Associate I. A Master’s Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. Coordinate and track workflows for regulatory submissions. ...

A Bachelor’s degree in a scientific field, preferably Chemistry or Pharmacy, with - years of experience, or a Master’s Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulator...

Assist in preparing product dossiers for regulatory submission to regulatory. Prepare and coordinate the compilation and/or submission of documents to regulatory agencies in support of maintenance and compliance requirements as well as development projects. You will be the primary contact and provid...

Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Degree in Regulatory Affairs with a minimum of months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulatory activities. ...

Bachelor’s degree in a scientific field, preferably Chemistry or Pharmacy, with 1-3 years of experience, or a Master’s Degree in Regulatory Affairs with a minimum of 3 months of regulatory experience (internship) is required. Help determine regulatory strategies for manufacturing changes and regulat...

The Associate Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines. Must have an extensive knowledge of regulatory requirements, including ICH and regional requirements, and have an under...

Plan and manage breakthroughs, feature interdependencies, project schedule, and overall quality of our product work you're doing. Assess, evaluate risks, and implement project work you're doing with urgency required to deliver business value. ...

Responsible for overseeing and managing facility-related projects from inception to completion. The ideal candidate will bring maturity and expertise to our project management process. ...

Vice President or Senior Vice President, Regulatory Affairs & Quality Assurance. Lead Regulatory Affairs and Quality Assurance functions. Meet has engaged on a search for a confidential search for a VP/SVP of Regulatory and Quality with one of our biotech clients. Manage all aspects of Regulatory su...

Liaise with colleagues in Regulatory Affairs therapeutics teams, local Affiliates, Regulatory Operations, Regulatory Project Management and third-party local agents to develop filing plans and deliver submissions to agreed priorities and timelines. Senior Manager, CMC Regulatory Affairs, Biologics. ...

The Senior Manager in Regulatory Affairs is responsible for developing and managing regulatory strategies to ensure compliance with U. Extensive knowledge of regulatory requirements, including ICH and regional guidelines, and an understanding of current global and regional trends in regulatory affai...

Senior Manager, Regulatory Affairs (Clinical). Meet has partnered with an exciting late-stage oncology biotech that is looking for a Senior Manager of Regulatory Affairs to join their team. You will support the preparation of major regulatory submissions (IND's, NDA's, BLA's). You will serve as the ...

The Executive Director/Senior Director of Regulatory Affairs will also oversee the preparation of all regulatory documents and submissions, mentor junior team members, and stay updated on changes in FDA and EU regulations. Executive Director/Senior Director of Regulatory Affairs. If you or someone y...

They are looking to bring on a Senior Director, Regulatory Affairs to the team. Provide strategic and operational leadership in regulatory affairs, including regulatory strategies, clinical study requirements, and marketing approvals in various regions. Utilize deep knowledge of regulatory requireme...

Senior Regulatory Affairs Specialist. Draft, edit, and compile technical documentation and design dossiers to support CE mark/UKCA mark regulatory filings. Prepare regulatory submissions for FDA 510(k) clearance and A2F submissions. Research regulatory requirements from FDA, CMDR, MDR, IVDR, and UK ...

This position manages the various employee benefits programs, this position does not have any direct reports. Attracts and retains employees by researching and explaining benefit programs. Recommends revisions and additions to the employee benefits program by examining and evaluating interest, estim...