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Pharmaceutical Regulatory Affairs Jobs in California

Below in the left colum are a few results based upon a basic search for Pharmaceutical Regulatory Affairs Jobs in California. Click the JOB TITLE to view detailed information, contact and application methods.

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In the right column are popular CareersInPharmaceutical.com searches specifc to Pharmaceutical Regulatory Affairs Industry employment. Clicking a link will display basic job search results for each term.

Job Search Results

SENIOR REGULATORY AFFAIRS SPECIALIST-

Santa Clara, California
Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based ...
Last Updated: 05/20/2013

Regulatory Affairs Specialist

California
  The Surgical Regulatory Affairs Specialist is responsible for US and EU registrations for surgical devices as assigned. Products include IOLs, Inserters, OVDs, Equipment, Instruments and S...
Last Updated: 05/20/2013

Regulatory Affairs Specialist: Operations

California
The Surgical Regulatory Affairs Specialist-Operations is responsible for supporting the Regulatory Affairs operations and process improvement activities under supervision of the Regulatory Affairs ...
Last Updated: 05/20/2013

Manager, Regulatory Affairs - Chemistry, Manufacturing and Controls

South San Francisco, California
  Responsible for coordination, gathering of information, and review of documents for CMC related documents for Regulatory submissions. Work closely with Regulatory and CMC staff...
Last Updated: 05/20/2013

Associate Director, Regulatory Affairs

South San Francisco, California
Essential/Primary Duties, Functions and Responsibilities Develop and implement strategies to facilitate the progress of Phase I through Phase IV development of drugs and biologics. Re...
Last Updated: 05/20/2013

Manager, Medical Writing

Foster City, California
The Medical Writing function resides organizationally within Regulatory Affairs at Gilead and provides scientific/regulatory writing services to support clinical trial reporting as well as a wide v...
Last Updated: 05/20/2013

Regulatory Affairs Mgr (Product Project Management)

Thousand Oaks, California
GPPM will be Responsible for: Providing project management support and coordinating achievement of deliverables for global regulatory, global safety, and regulatory CMC subfunction project ...
Last Updated: 05/20/2013

Regulatory Affairs Mgr (Product Project Management)

Thousand Oaks, California
GPPM will be Responsible for: Providing project management support and coordinating achievement of deliverables for global regulatory, global safety, and regulatory CMC subfunction project ...
Last Updated: 05/20/2013

Exec Dir Regulatory Promotion and Material Compliance Functional Head

Thousand Oaks, California
The Global Regulatory Affairs and Safety (GRAAS) US Regulatory organization is looking for an Executive Director, Regulatory Promotion and Material Compliance Functional Head. This position wi...
Last Updated: 05/20/2013

Regulatory Writing Mgr

Thousand Oaks, California
This position could be located in Thousand Oaks California, South San Francisco California, or at a remote home office. Job Summary: Write, rewrite, and edit and gain senior management ap...
Last Updated: 05/20/2013

Regulatory Writing Mgr

Thousand Oaks, California
Write, rewrite, and edit and gain senior management approval of scientific and regulatory documents that comply with global regulatory standards. Serve as functional area lead on product teams. T...
Last Updated: 05/20/2013

Sr Finance Manager, Regulatory, Quality & Compliance

South San Francisco, California
The Senior Finance Business Partner will support senior leaders in Technical Regulatory and Quality and Compliance (RQC).  Quality & Compliance, the broadest Functional Unit of the PT netw...
Last Updated: 05/20/2013

Associate Director, Technical Regulatory Team Program Management

South San Francisco, California
Technical Regulatory is a global function that supports strategic regulatory and submission activities for the Roche and Genentech product portfolio. Support of individual portfolio projects is man...
Last Updated: 05/20/2013

Regulatory Affairs Mgr (CMC Systems)

Thousand Oaks, California
The CMC Systems group is responsible for developing, maintaining and improving the practices and procedures used to streamline and coordinate investigational and marketing applications. This group ...
Last Updated: 05/20/2013

Program Director, Regulatory CNS/Metabolism

South San Francisco, California
Regulatory Program Management is part of the broader PDR organization that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and presen...
Last Updated: 05/20/2013

Sr Regulatory Product Manager/Scientist

South San Francisco, California
In the position of Senior Regulatory Product Manager in Technical Regulatory Affairs, you will be accountable for the preparation of regulatory submissions and strategies supporting the product&rsq...
Last Updated: 05/20/2013

Global Regulatory Leader (Oncology)

South San Francisco, California
Global Regulatory Leader   Accountable for regulatory management of a project(s) and leading a matrix team of regulatory professionals.   Primary Responsibilities and Acco...
Last Updated: 05/20/2013

Senior Regulatory Product Manager/ Reg. Scientist

South San Francisco, California
The Technical Regulatory Senior Product Manager will be responsible for developing global regulatory strategy, writing high quality dossiers, and leading teams for assigned projects to obtain timel...
Last Updated: 05/20/2013

Associate Program Director, Regulatory Small Molecule Development

South San Francisco, California
As a product manager, you will be responsible for supporting the preparation, assembly, and review of both product and facility-related Chemistry Manufacturing and Controls (CMC) regulatory submiss...
Last Updated: 05/20/2013

View All Pharmaceutical Regulatory Affairs Jobs

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