Average salary: $130,000 /yearly
More stats ...application is true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs or related field plus...
Suggested
Full time
Remote job
...Responsibilities:
ROLE AND RESPONSIBILITIES:
Manage Lupins existing REMS programs and help in the development of new... ...operations
Responsible for maintaining and updating various regulatory databases to ensure accuracy of information
Any additional responsibilities...
Suggested
...the Best Workplaces in Biopharma™, Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.
Overview
The Manager, Regulatory Operations will be responsible for functional activities related to US/Ex-US regulatory submissions. In addition, this individual...
Suggested
Holiday work
Temporary work
Flexible hours
...therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Regulatory Data Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence function, responsible for driving data...
Suggested
PwC
PLS Regulatory Senior Manager
Florham Park ,
New Jersey
Apply Now
Specialty/Competency:
Conduct and Compliance
Industry/Sector:
Pharma and Life Sciences
Time Type:
Full time
Travel Requirements:
Up to 40%
A career within Regulatory Risk and Compliance services...
Suggested
Full time
H1b
...our journey!
To learn more about ADC Therapeutics, please visit us at and follow us on LinkedIn .
What You'll Do :
As the Manager, Regulatory Operations and Submissions Management, this position will lead regulatory operations activities and support and manage US and...
Suggested
Full time
Remote job
Worldwide
Flexible hours
...employment application is true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA with the following requirements: Bachelor’s degree in a scientific...
Suggested
Full time
Remote job
Worldwide
...Manage Lupin's existing REMS programs and help in the development of new REMS programs (as needed) with the support of the supervisor... ...REMS and other patient safety programs. Works closely with Phar Regulatory Affairs, Manager, Regulatory, Operations, Product Development,...
Suggested
...The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development...
Suggested
Local area
...communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including... ...regulatory strategies for in-line products through life cycle management programs.
Contribute A&P expertise to the development of...
Suggested
Work experience placement
Summary
This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation... ...to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory...
Suggested
Contract work
...sustainable, clean energy future through our subsidiary, Suburban Renewables!
We have an exciting opportunity for a Regulatory Compliance Manager Renewable Natural Gas (RNG), who will be responsible for developing, maintaining, and enforcing company compliance policies...
Suggested
Temporary work
Local area
Immediate start
...novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Manager, Regulatory Affairs – Regulatory Project Management (RPM) provides planning and coordination supports for global and US regulatory...
Suggested
Work experience placement
...employment application is true to the best of my knowledge.
Job Description Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs, Marketed Products in Cambridge, MA with the following requirements: Bachelor degree in Pharmacy, Pharmaceutical...
Suggested
Full time
Remote job
Management Expert
Contribute to the development of PSRs, when applicable, with the support of GSO or LSO
Track the actual implementation... ...policy
Maintain and update the local quality documents
PV Regulatory Intelligence
Ensure appropriate implementation and monitoring...
Suggested
Local area
Remote job
..., please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
Senior Manager, Global Regulatory Strategy, US & Canada, AbbVie Inc., Madison / Florham Park (Morris County) New Jersey
Responsible for the development...
Holiday work
Temporary work
...UDI related master data for submission to UDI databases.
Complete UDI database submissions (e.g. US GUDID)
Support and advise on regulatory requirements for UDI direct part marking compliance
Assign and maintain the EU Basic UDI for Client portfolio
Provide the regulatory...
...:
We are seeking a life-sciences professional with healthcare regulatory experience to serve as the Director of Regulatory Affairs within... ...The Director of Regulatory Affairs plays a vital role in the management of clients, billable projects, and staff. This position is...
Holiday work
Temporary work
Work experience placement
Flexible hours
...space (e.g.,
Houston, TX )
J&J Family of Companies
Director, Regulatory Affairs
in
Raritan ,
New Jersey
Director, Regulatory Affairs... ...strategies, PMR fulfillments, and other US-related issues. Manage routine maintenance submissions. Manage and track NA post-approval...
Holiday work
Full time
Temporary work
Remote job
...protocols, changes requests, gap & root cause analysis, risk management plans, traceability matrix, summary reports for facilities, equipment... ...& submission of documentation for quality compliance & regulatory authorities. Skills required: EU MDR, ISO 13485, cGmp, IQ/OQ/PQ...
