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Full-Time Global Regulatory Manager jobs in Summit, NJ

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SYSTEM MANAGEMENT & REGULATORY SPECIALIST

Ensure proper execution of technical controls associated with regulatory compliance programs including NERC CIP, SOX, BPU and FERC Affiliate Restrictions. Manage patching cycles for workstations and servers associated with Securit...

CompanyPseg
AddressNewark, NJ
CategoryInformation Technology
Job typeFull-Time
Date Posted 3 days ago See detail

System Management & Regulatory Specialist

Pseg

Newark, NJ

Ensure proper execution of technical controls associated with regulatory compliance programs including NERC CIP, SOX, BPU and FERC Affiliate Restrictions. Manage patching cycles for workstations and servers associated with Securit...

3 days ago seen See more...

Senior Director, Global Regulatory Intelligence & Policy

Biospace

Basking Ridge, NJ

Leads day-to-day a team of Regulatory Intelligence Policy professionals across all major regions, incl. mentorship, performance mgmt., etc. Supports the team in both Regulatory Intelligence (collection, interpretation and communic...

2 weeks ago seen See more...

Regulatory Associate Technical Manager

Givaudan

East Hanover, NJ

Manage the end-to-end lifecycle of electronic regulatory documentation templates. Identify enhancements of existing solutions with the intent support critical business needs. Build reusable tools to streamline the CoE operational...

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...

2 months ago seen See more...

Director, Global Project Management and Leadership - Disease Area Strategy

Biospace

Basking Ridge, NJ

Project Responsibilities: Independently manage or lead strategy development on Global Project Teams (GPT) for drug development projects in any phase of development. Develops and maintains a high performing team. Manages the GPT in...

2 weeks ago seen See more...

Executive Director, Global Clinical Operations Study Management Group Head

Biospace

Basking Ridge, NJ

With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medic...

3 weeks ago seen See more...

Regulatory Compliance Senior Manager - Parsippany, NJ

Teva Pharmaceuticals

Parsippany, NJ

Responsible to execute the formal market action decision as dictated by Senior Quality Unit Management and the Market Action Committee and author Product Recall Letter. Circulate draft Recall Letter to Quality Unit Management for...

3 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...

a month ago seen See more...

Clinical Trial Manager, Global Oncology Medical Affairs

Biospace

Basking Ridge, NJ

Support the preparation, set-up, and execution and reporting of all Global Oncology Medical Affairs operations Clinical Trial activities, ensuring adherence to timelines, budgets, project, and quality plans, and relevant ICH/GCP G...

3 weeks ago seen See more...

Sr. Director, Global Project Management

Biospace

Basking Ridge, NJ

Project ResponsibilitiesIndependently manage or lead strategy development for high complexity drug development projects/programs. Manages the Global Project Team(s) in partnership with the Global Team Leader to drive strategy deve...

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...

2 months ago seen See more...

Quality and Regulatory Manager Nutraceuticals

Ashland, Llc

Kearny, NJ

Develops, implements, monitors, and continuously improves programs to ensure compliance with industry standards for food and dietary supplements (cGMP, 21 CFR 111, 117, HACCP, FSMA, SQF, etc.). Supports customer & other regulator...

a month ago seen See more...

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