Cfr $100,000 jobs in New Jersey

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Sr Scientist
Mondelez International - 1,101 reviews - Parsippany, NJ 07054
Proficiency in understanding and application of fundamental and basic FDA - CFR regulations that impact Biscuit and Confectionary products to apply to...
Sponsored by Mondelēz International
Associate Director, Clinical Supplies Management
Allergan - 470 reviews - Jersey City, NJ
Willingness and ability to follow SOPs and applicable regulations from CFR. The Associate Director, Global Clinical Supplies provides functional leadership to...
Sponsored
Vice President, Regulatory Affairs - Generics (SAN DIEGO)
San Diego Pharmaceuticals - Monmouth Junction, NJ
Thorough understanding of the CFR, FDA/ICH guidelines and cGMP’s, as they pertain to parenteral pharmaceuticals. Company Sponsored Relocation to San Diego \*\*....
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Sponsored

Sr Scientist

Mondelez International - 1,101 reviews - East Hanover, NJ 07936
Proficiency in understanding and application of fundamental and basic FDA - CFR regulations that impact Biscuit and Confectionary products to apply to...

Consultant- Medical Devices Reporting

Maven Workforce LLC - Bridgewater, NJ
Reportability in accordance with 21 CFR 803 and to ensure timely submission of reports to the.  In-depth Knowledge of the Medical Device Reporting process and...
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Validation Engineer

ITvorks - Somerset, NJ 08873
$55 an hour
\*\*21 CFR Part 11 assessment. 11-12 Years experience in Life sciences, CSV....
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Principal Scientist

Bristol-Myers Squibb - 537 reviews - Princeton, NJ 08540
Knowledge of GLPs, 21 CFR Part 58, Bioanalytical Guidance (FDA, EMA), Immunogenicity Guidance (FDA, EMA) is desirable....

Packaging Engineer

Bristol-Myers Squibb - 537 reviews - New Brunswick, NJ
Strong understanding of packaging materials testing and performance requirements defined by ASTM, ISTA, CFR and FDA Guidance’s....

MANAGER, Q-CSV

Johnson & Johnson Services Inc. - 1,753 reviews - Bridgewater, NJ
Thorough knowledge required of cGMP regulations related to CSV, including 21 CFR Part 11, Part 210, Part 211 and Part 820....

Tech Expert

Bayer - 1,436 reviews - Whippany, NJ
Your tasks and responsibilities The primary responsibilities of this role, Technical Expert, are to: Establish implementation strategy for software,...

Program/ Project Manager - Life Sciences

Cambridge Semantics - New Jersey
Strong understanding of Life Science quality management practices including GxP validation and 21 CFR Part 11....

Staff Quality Engineer

Orthoclinical - Raritan, NJ
Job ID 2016-3773 # of Openings 1 Job Locations US - NJ - Raritan Posted Date 12/1/2016 Category Quality Assurance & Quality Compliance More...

Quality Engineer - Devices

Teva Pharmaceuticals - 265 reviews - Ewing, NJ
FDA 21 CFR Part 820, 21 CFR Part 4, ISO 13485 ) Identify gaps and recommend remediation. Working experience with medical device GMP Quality Systems and related...
Sr. Quality Auditor
CFR 210/211, ISO 13485; Knowledge of Good Manufacturing Practices (GMPs), Quality System standards and regulatory requirements such as 21 CFR 820;...
Sponsored
Regulatory Affairs Manager
Strong knowledge of quality system requirements specifcially ISO 13485 and FDA’s 21 CFR Part 820. Regulatory Affairs Manager....
Sponsored by Kavo Kerr Group

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