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Regulatory Affair Associate jobs in Piscataway, NJ

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ASSOCIATE DIRECTOR, REGULATORY AFFAIRS

Provide Regulatory support and guidance in the development, revision, review, and approval of labeling artwork for Health Authorities submissions, as well as any post marketing labeling changes. Responsible for post approval lifec...

CompanyBausch + Lomb
AddressBridgewater, NJ
CategoryInformation Technology
Job typeOther
Date Posted 4 weeks ago See detail

Associate Director, Regulatory Affairs

Bausch + Lomb

Bridgewater, NJ

Provide Regulatory support and guidance in the development, revision, review, and approval of labeling artwork for Health Authorities submissions, as well as any post marketing labeling changes. Responsible for post approval lifec...

4 weeks ago seen See more...

Associate Manager, Regulatory Affairs (Remote)

Iff Family Of Companies

Dayton, NJ

Responsible for overall management of the pet product portfolio. Draft submissions such as US feed GRAS, and US AAFCO submissions. Draft submissions and provide regulatory guidance to R&D groups for businesses such as Food Enzymes...

2 months ago seen See more...

Associate Director, Regulatory Affairs

Johnson And Johnson

Somerville, NJ

Bring innovative regulatory approaches, deeply rooted in science, to lead the team in discussions with FDA and Health Canada to find the best development strategies for novel therapies in the areas where no other precedents exist....

4 weeks ago seen See more...

Director, Regulatory Affairs Strategy, Hematology New

Biospace

Basking Ridge, NJ

Provide interpretation of regulatory authorities feedback, policies and guidelines. Lead the development of regulatory strategic plans either directly in conjunction with project teams or through your reports. Own the preparation...

14 hours ago seen See more...

Senior Administrative Associate - Regulatory Affairs

Merck Sharp & Dohme

Rahway, NJ

$78,700 - $123,800 a year

General secretarial/clerical tasks including scheduling of complex meetings, management of calendar, filing of monthly expense reports for multiple therapeutic area regulatory liaisons General support of the Rahwaybased staff, as...

2 months ago seen See more...

Associate Director, US Regulatory Affairs Strategy

Daiichi Sankyo, Inc.

Basking Ridge, NJ

Develop and implement US regulatory strategy for assigned project(s). Strategize and plan for FDA meetings for assigned product. Liaise, negotiate and orchestrate meetings with FDA. Prepare internal meeting minutes to capture the...

4 weeks ago seen See more...

Associate Director, Medical Affairs - Program Management

Merck

Rahway, NJ

Support the SRO Lead in the execution of extensive, global initiatives, ensuring the program objectives and timelines are consistently met.. Facilitate the creation and approval of all project deliverables, including maintaining d...

6 days ago seen See more...

Associate Manager, Regulatory Affairs

Kenvue

Skillman, NJ

Understand the Regulatory landscape for Consumer products and effectively manage regulatory priorities and timelines for marketed products and will support regulatory strategy for innovative projects across many regulatory classif...

4 weeks ago seen See more...

Associate Manager, Regulatory Affairs

Johnson & Johnson Consumer Inc.

Skillman, NJ

Understand the Regulatory landscape for Consumer products and effectively manage regulatory priorities and timelines for marketed products and will support regulatory strategy for innovative projects across many regulatory classif...

4 weeks ago seen See more...

Director, Global Regulatory Affairs (GRL)

Biospace

Basking Ridge, NJ

Manages, directs, and drives the strategy for all Regulatory activities associated with the registration and support of new and approved drug products. Seeks and incorporate regional and functional RA strategy into a global strate...

3 weeks ago seen See more...

Director, Regulatory Affairs Companion Diagnostics

Biospace

Basking Ridge, NJ

CDx development: Provide critical strategic and tactical regulatory guidance for CDx/IVD development and CDx submission plan for each country/region, both before and after CDx testing. At the time of implementation of a CDx study/...

3 weeks ago seen See more...

Regulatory Project Manager (RPM), Associate Director

Merck Sharp & Dohme

Rahway, NJ

$122,800 - $193,300 a year

Demonstrates strong project management skills in handling projects of significant complexity within the end-to-end regulatory drug development process. Proactively identifies areas that need Regulatory Project management support a...

a month ago seen See more...

Manager, Regulatory Affairs - Regulatory Project Manager

Daiichi Sankyo, Inc.

Basking Ridge, NJ

$117K - $148K a year

Plan, coordinate, and review US regulatory submissions in collaboration with USRL, Regulatory Operations (RO), and other key stakeholders (e.g. Protocol Amendments, Form 1572s, Information Amendments, Meeting Requests/Background M...

a month ago seen See more...

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What companies are hiring for Regulatory Affair Associate jobs in New Jersey?

The top companies hiring now for Regulatory Affair Associate jobs are Capleo Global,

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