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Sr. Manager QA/Contract Manufacturing
Cameron Craig Group - Plainsboro, NJ
$110,000 - $160,000 a year
Demonstrated knowledge of regulations including FDA 21 CFR 820, 1270 and 1271, AATB requirements, ISO 9001, ISO 13485, CMDR, Medical Device Directive Regulation...
Easily apply
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Director - Clinical Data Management
Job Juncture - Princeton, NJ
$120,000 - $160,000 a year
Demonstrated knowledge of GCPs, ICH guidelines, CFR Part 11 and computer systems validation. Our client, a well established international contract research...
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Director, Clinical Development Gastrointestinal
Job Juncture - Madison, NJ
$215,000 - $230,000 a year
ICH, PhRMA and CFR guidelines, as well as Company’s policies, SOPs and Work Instructions. As a result the percentage of time spent across the roles for which...
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Director QA Compliance

The Getinge Group - 11 reviews - New Jersey
Must be competent with 21 CFR 820, 801, 803, 806 and any other applicable federal regulations, and Quality standards (As applicable to your job function)....

Vice President, Regulatory Affairs (ANDA) - SAN DIEGO

San Diego Pharmaceuticals (Generics) - Elizabeth, NJ
Thorough understanding of the CFR, FDA/ICH guidelines and cGMP’s, as they pertain to parenteral pharmaceuticals....
Easily apply

Manager IT Portfolio Management

Otsuka Pharmaceutical - 13 reviews - Princeton, NJ
Knowledge of global computer system regulatory requirements as they relate to systems development, testing, and validation preferred including 21 CFR Part 11...

Staff Regulatory Affairs Specialist (Trauma)

Stryker - 455 reviews - Mahwah, NJ
Extensive knowledge of FDA Quality System Regulations (21 CFR), EU Medical Device Directives (MDD), applicable guidance documents, and additional international...

Corporate Risk – External Regulatory Risk Reporting - Analys...

JPMorgan Chase - 11,452 reviews - Jersey City, NJ
JPMC compliance with the 12 CFR regulations. Corporate Risk – External Regulatory Risk Reporting - Analyst....

Associate Director, Business Information Management

Allergan - 484 reviews - Rockaway, NJ
Understanding of compliance and regulatory standards e.g. ICH, 21 CFR Part 11, SDLC, GxP validation guidelines as well as all Allergan policies, and procedures....

Senior Manager, IT Regulatory Compliance

JANSSEN SUPPLY GROUP, LLC - Raritan, NJ
Expert knowledge of Quality System regulations, ISO, ICH, PIC/S, and cGMP regulations, including Annex 11, 21 CFR Part 11, Part 210, Part 211 and Part 820, and...

Validation Consultant

Supply Chain Wizard - Princeton, NJ 08540
Manage adherence with 21 CFR Part 11 for assigned validation consultancy systems. NY/NJ/PA Tri State Area....

IT Manager PLO Product Development – Consumer R&D Operating...

J & J Consumer Inc. - Skillman, NJ
Experience with software validation (21 CFR Part 11) in GxP regulated environments is required. Johnson & Johnson Consumer IT is recruiting for an IT Manager...

QA Lead-Full Time

CavalierIT - Wayne, NJ
$60 an hour
Thorough knowledge of cGMP regulations related to CSV including 21 CFR Part 11, and GAMP standards are required. Computer System Validation....
Easily apply
Sr. Manager QA/Contract Manufacturing
Hotclinicaljobs.com - Plainsboro, NJ
Demonstrated knowledge of regulations including FDA 21 CFR 820, 1270 and 1271, AATB requirements, ISO 9001, ISO 13485, CMDR, Medical Device Directive Regulation...
Easily apply
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Sr. Contract Manufacturing Manager - FDA Regulated Experienc...
Job Juncture - Plainsboro, NJ
$110,000 - $160,000 a year
Demonstrated knowledge of regulations including FDA 21 CFR 820, 1270 and 1271, AATB requirements, ISO 9001, ISO 13485, CMDR, Medical Device Directive Regulation...
Sponsored

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