Job offers: regulatory affairs specialist washington

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QC/QA Manager

The Judge Group :: South Bend, Indiana :: over 30 days ago

... RELOCATION: Relocation Assistance Available Manager provides servant leadership in all areas of food safety, quality and compliance. The manager is the liaison for regulatory personnel including onsite inspectors. The Manager provides management to all Quality and Food Safety Supervisors and technicians. DUTIES AND RESPONSIBILITIES Oversee ...

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Manufacturing Manager

The Judge Group :: La Grange, North Carolina :: over 30 days ago

... problems to ensure minimum cost and prevent operation delay. Manage product yield material usage and material loss data. Maintain compliance with company policies, regulatory requirements, quality specifications, safety standards and sanitation practices. Monitor and coordinate maintenance schedule as well as controlling costs of ...

Regulatory Affairs Project Manager

Cameron Craig :: Fort Lauderdale, Florida :: over 30 days ago

Established, growing pharmaceutical manufacturer is seeking a Regulatory Affairs Project Manager for their Fort Lauderdale area location. THE REGULATORY AFFAIRS PROJECT MANAGER POSITION IS OPEN DUE TO GROWTH AND RELOCATION ASSISTANCE TO SUNNY SOUTH FLORIDA IS AVAILABLE. The Regulatory Affairs Project Manager will be responsible for US Regulatory ...

Associate Director of Regulatory Affairs Strategy

Global Personnel Search Inc :: North Chicago, Illinois :: yesterday

_ASSOCIATE DIRECTOR OF REGULATORY AFFAIRS STRATEGY - GLOBAL / ONCOLOGY_ NORTH CHICAGO,ILLINOIS _POSITION SUMMARY:_ Accountable for the production of submission documents using electronic document management systems. Author, review, and submit new applications, supplements, reports and amendments, along with responses to Regulatory Agencies in the ...

Associate Director Regulatory Affairs, CMC Northeast

Cameron Craig :: New Jersey :: 10 days ago

ASSOCIATE DIRECTOR REGULATORY AFFAIRS, CMC NORTHEAST * Liaison between company and regulatory agencies for submissions and CMC issues * Develop submission strategies leading to approvals of applications. * Prepare, review, and create submissions and CMC sections for regulatory filings * Manage relationships with business stakeholders with ...

Sr. Mgr./Associate Director - Regulatory Affairs

Cameron Craig :: New Jersey :: yesterday

Our client, a major Pharmaceutical Company in the Central NJ area, is looking for a Sr. Mgr./Associate Director - Regulatory Affairs. The Sr. Mgr./Associate Director Regulatory Affairswill oversee a variety of projects (IND/NDA/BLA), and they will manage these projects through all phases of development as well as be involved with both post-approval ...

Associate Director, Regulatory Affairs - Global /

Elite Executive Search :: 9 days ago

ASSOCIATE DIRECTOR, REGULATORY AFFAIRS - GLOBAL / ONCOLOGY - MIDWEST * Responsible to write and file electronic submissions, manage projects and project deadlines * Create and implement regulatory strategy for North America * Be part of project decisions and as the Associate Director make the appropriate recommendations for project improvement * ...

Regulatory Affairs - Manager / Sr. Manager

Cameron Craig :: Paramus, New Jersey :: over 30 days ago

Our client, a Major Global Pharmaceutical Company, is actively expanding their operations in the ***. They are currently looking for a Manager/Sr. Manager, Regulatory Affairs. The Manager/Sr. Manager will be responsible for submissions (IND/NDA/BLA) from "Cradle to Grave" - as well as the developmentand execution of global regulatory ...

Regulatory Affairs Intern

Noven Pharmaceuticals :: New York, New York :: 2 days ago

Regulatory Affairs Intern - (952) Job Title Regulatory Affairs Intern Location New York Office - New York, NY 10118 US (Primary) Category R & D/Product Development Employment Status Intern Exemption Type Non-Exempt Shift Type First Shift Job Description Position: Paid Summer Internship - Pharmaceutical Industry. Company: Noven Pharmaceuticals, ...

Regulatory CMC Change Control Specialist (2511)

BioPoint :: Lexington, Massachusetts :: yesterday

BioPoint is seeking to hire a Regulatory CMC Change Control Specialist for a position in Lexington, MA. DESCRIPTION Global Regulatory Affairs Chemistry, Manufacturing and Controls (CMC) The incumbent will assist in the management of change controls for the CMC regulatory affairs group for all biological, plasma and/or small molecule products. This ...

Regulatory Affairs Manager

Cameron Craig :: Boston, Massachusetts :: over 30 days ago

Were currently working with a food manufacturing client to help the identify a Regulatory Affairs Manager. Our client is a fast-growing food manufacturer in the Boston area. This individual will have 1 direct report and sit within the Research and Development group. Theyll work directly with R&D and QA to develop ingredient statements, ...

Director, Regulatory Affairs

Cameron Craig :: Massachusetts :: 10 days ago

DIRECTOR, REGULATORY AFFAIRS / CMC A key leadership position in the therapeutic area of Oncology. Responsibilities include all development activities, marketed products, including CMC, labeling changes, and regulatory compliance of marketed products. Position requires a leader who can generate and effectively implement all strategic initiatives and ...

Regulatory Affairs Specialist

Piper Companies :: Durham, North Carolina :: over 30 days ago

Job Description: Regulatory Affairs Specialist Piper Clinical Solutions is actively seeking an entry- to mid-level Regulatory Affairs Specialist to work with an international medical device company in the Raleigh-Durham (RTP) area. The Regulatory Affairs Specialist will be working on a team that supports international submissions, and will be ...

Regulatory Affairs Manager

Two95 International Inc. :: Philadelphia, Pennsylvania :: over 30 days ago

Title: Regulatory Affairs Manager Location: Philadelphia, PA Duration: 6 month C2H Interview: Phone & F2F Start: 12/5/2016 Skills: * Bachelors degree, preferably in a science-related discipline * Minimum of five years experience in pharmaceutical regulatory affairs operations, with a good understanding of drug development * Recent direct line ...

Sr. Director, Regulatory Affairs

GTS :: Hayward, California :: 18 days ago

Join our exciting organization and work side by side with top industry experts from around the world! This is an exciting time for us and we are seeking a seasoned Regulatory Affairs professional to step into this executive level role! If you enjoy projects that are both challenging & rewarding we would love to meet you! Reporting directly to ...

Regulatory Affairs Associate (439031)

Advanced Clinical :: San Rafael, California :: over 30 days ago

Job Description: OVERVIEW:The Associate, Regulatory Affairs will be assisting the regulatory team in supporting clinical and/or nonclinical studies. RESPONSIBILITIES:Coordinate the preparation and submission of domestic and international regulatory submissions related to clinical and nonclinical aspects of 0product development, including the ...

Regulatory Affairs Associate (Pharmaceuticals) (4428)

BioPoint :: Lake Forest, Illinois :: 14 days ago

BioPoint is looking for a Regulatory Affairs Associate for a support role in Lake Forest, IL. PRIMARY FUNCTION: Provides regulatory affairs support and expertise supporting US and global registrations of infusion pumps and related accessories Provides regulatory support to assigned products/teams. Tracks and documents regulatory deliverables and ...

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