Regulatory Specialist Jobs in Old Bridge, New Jersey | ComplianceCrossing.com
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Regulatory Specialist Jobs in Old Bridge






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SPONSOREDJOB
Location
Bridgewater, NJ
Posted Date
Nov 21,17
Source
Employer   
Total Views
2

regulatory specialist in Bridgewater New Jersey Responsibilities ... New Jersey Responsibilities JOB TITLE: regulatory specialist LOCATION: Bridgewater, NJ REPORTS TO: ... Senior Manager, Product Assurance and regulatory Affairs (PARA) Ingredion..

 
Location
Kenilworth, NJ
Posted Date
Sep 06, 17
Info Source
Employer  - Full-Time   
Total Views
42

Senior Specialist, Global Trade Compliance-COM000539 DESCRIPTION Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified ..

 
Location
Kenilworth, NJ
Posted Date
Sep 20, 17
Info Source
Employer  - Full-Time   
Total Views
31

Global Trade Compliance Specialist - Trade Data-COM000540 DESCRIPTION Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with ..

 
Location
New Brunswick, NJ
Posted Date
Nov 07, 17
Info Source
Recruiter  - Full-Time  
Total Views
2

Job Title: Compliance Specialist Work Location: New Brunswick, NJ Length of Assignment: 6 Months Client: A Big Pharmaceutical Company Job Description: • Managing and coordinating activities related to cGMP Enterprise Electronic ..

 
Company
Location
New Brunswick, NJ
Posted Date
Nov 10, 17
Info Source
Recruiter  - Full-Time   
Total Views
4

Summary Managing and coordinating activities related to cGMP Enterprise Electronic Systems. Duties include leading, developing, and maintaining compliance activities across IT Enterprise Services supported regulated GPS applications. Responsible for developing policies ..

 
Location
Bridgewater, NJ
Posted Date
Nov 14, 17
Info Source
Employer  - Full-Time   
Total Views
1

Job Description: Experience in GDUFA pharmaceutical/biopharmaceutical industry or related industry/cGMP environment. Good understanding of scope and requirements for Module 3 content as well as drug and drug substance manufacturing change controls ..

 
Location
Bridgewater, NJ
Posted Date
Nov 14, 17
Info Source
Recruiter  - Full-Time  
Total Views
5

Job Title: Regulatory Affairs Specialist III Duration: 13 months Location: Bridgewater, NJ Client : A Big Pharmaceutical Client Duties: Experience in GDUFA pharmaceutical/biopharmaceutical industry or related industry/cGMP environment. Good understanding of ..

 
Company
Location
Bridgewater, NJ
Posted Date
Nov 14, 17
Info Source
Recruiter  - Full-Time   
Total Views
3

Experience in GDUFA pharmaceutical/biopharmaceutical industry or related industry/cGMP environment. Good understanding of scope and requirements for Module 3 content as well as drug and drug substance manufacturing change controls to be ..

 
Location
Bridgewater, NJ
Posted Date
Nov 21, 17
Info Source
Employer  - Full-Time   
Total Views
2

Regulatory Specialist in Bridgewater New Jersey Responsibilities ... New Jersey Responsibilities JOB TITLE: Regulatory Specialist LOCATION: Bridgewater, NJ REPORTS TO: ... Senior Manager, Product Assurance and Regulatory Affairs (PARA) Ingredion..

 
Location
Summit, NJ
Posted Date
Nov 19, 17
Info Source
Employer  - Full-Time   
Total Views
2

Duties: Author technical documents in internal Documentum system. Perform technical writing and authoring CMC documents following ICH and GMP guidelines Expected to stay well-organized, work with minimal management, and meet aggressive ..

 
Location
Plainsboro, NJ
Posted Date
Nov 21, 17
Info Source
Employer  - Contract     
Total Views
2

NCS has been helping enterprises staff and deliver business-critical projects for over 30 years. We are business and technology consultants who understand what works when aligning the resources needed for success. ..

 
Location
Basking Ridge, NJ
Posted Date
Nov 23, 17
Info Source
Recruiter  - Full-Time  

... is in search of multiple Regulatory Affairs Specialists and Associates. If ... field preferred Experience working with regulatory documentation and submitting to external ... regulations SUMMARY OF POSITION: The..

 
Company
EPM Scientific
Location
Bedminster, NJ
Posted Date
Nov 22,2017
Info Source

Experience with ex-US regulatory authorities Company Description EPM Scientific is a global specialist recruitment company working exclusively in the Life Sciences industry. As an industry expert we .....

 
Company
Chenoa Information Services
Location
Bridgewater, NJ
Posted Date
Nov 21,2017
Info Source

Thorough understanding and familiarity with GMP Regulation, including 21 CFR 210 & 211, ICH Guidelines, FDA Guidance Documents and DEA Regulations, Empower, ELN and LIMS.MAIN RESPONSIBILITESReview .....

 
Company
Scientific Search
Location
Princeton, NJ
Posted Date
Nov 14,2017
Info Source

Regulatory Affairs Associate (Job# JB2-12490) The individual selected for this position will be responsible for the following listing of duties to assure compliance with applicable regulatory .....

 
Company
EPM Scientific
Location
Edison, NJ
Posted Date
Nov 09,2017
Info Source

Senior Regulatory Publisher (contract) My client in New Jersey is looking to bring a Senior ... Company Description EPM Scientific is a global specialist recruitment company working exclusively .....

 
Company
eclaro
Location
New Brunswick, NJ
Posted Date
Nov 08,2017
Info Source

Ensures compliance with all Company policies and procedures, including safety rules and regulations.Partners with IT Validation to ensure risk assessments, incident management and oversight are .....

 
Company
Abel HR
Location
Cranbury, NJ
Posted Date
Oct 31,2017
Info Source

... regulations, as well as internal policies and procedures, the Quality Control Specialist will evaluate consumer/ home equity loan products to ensure compliance with lending guidelines/ policies .....

 
Company
Rochester Regional Health
Location
newark, New Jersey
Posted Date
Oct 08,2017
Info Source

SUMMARYAs a Clinical Regulator Compliance - RN you will provide and supports regulatory, accreditation and certification activities to achieve and sustain..

 
Company
Raritan Pharmaceuticals
Location
East Brunswick, NJ
Posted Date
Oct 07,2017
Info Source

Compile, prepare, and submit routine regulatory documents and provide support for various regulatory activities related to cGMPs, FDA and audit firms. * Interact with Research & Development, Quality .....

 
Company
Whitman
Location
Cranbury Township, NJ
Posted Date
May 23,2016
Info Source

Whitman is currently seeking a Due Diligence Specialist / Senior Environmental Scientist to join ... Interaction and coordination with clients, subcontractors, and regulatory agency staff..

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