Regulatory Affairs Specialist Jobs in USA

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Regulatory Affairs Project Manager Nutrition Colum...

Abbott

profile Columbus - USA

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

17 days ago
Full Time

Director – Cmc Regulatory Affairs (gene Therapy)

Stark Pharma Solutions Inc

profile Piscataway - USA

Hi My name is Karthik Mutyala from Stark Pharma Solutions Inc we are hiring talents for our client. I am working on Director CMC Regulatory Affairs position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job descript...

17 days ago
Full Time

Principal Regulatory Affairs Specialist Pelvic Hea...

Medtronic

profile Minneapolis - USA

We anticipate the application window for this opening will close on - 25 Jul 2026Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put...

18 days ago
Full Time

Regulatory Affairs Project Manager

Colgate

profile Piscataway - USA

No Relocation Assistance OfferedJob Number#173814 - Piscataway New Jersey United StatesWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care Personal Care Home Care Skin Care and Pet Nutrition. Our products are trusted in...

18 days ago
Contract

Regulatory Affairs Strategy Manager (oncology)

Exelixis

profile Alameda - USA

SUMMARY/JOB PURPOSE: Responsible for managing and maintaining existing Investigational New Drug (IND) Clinical Trial Application (CTA) New Drug Application (NDA) and Biologics Licensing Application (BLA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates...

18 days ago
Full Time

Senior Program Director (commercial Regulatory Aff...

Dawar Consulting, Inc.

profile South San Francisco - USA

Our client a world leader in biotechnology and life sciences is seeking a "Senior Program Director Commercial Regulatory Affairs". Location: South San Francisco CA (Fully Remote)Duration: Long-Term Contract (Possibility Of Further Extension)Pay Rate: $120-$127/hr on W2Company Benefits: Medical Denta...

18 days ago
Full Time

Senior Manager Regulatory Affairs, Chemistry, Manu...

Abbvie

profile Waltham - USA

The Senior Manager Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics products to patients including mAb ADC and cell & gene therapies. Prepares CMC regulatory strategies that enable first pass...

19 days ago
Full Time

Senior Manager Regulatory Affairs, Chemistry, Manu...

Abbvie

profile North Chicago - USA

The Senior Manager Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics products to patients including mAb ADC and cell & gene therapies. Prepares CMC regulatory strategies that enable first pass...

19 days ago
Full Time

Community Affairs Specialist

Office Of The Illinois State Treasurer

profile Chicago - USA

JOB OPPORTUNITY ANNOUNCEMENTPosition: Community Affairs Specialist (2 vacancies) Division: Civic Engagement Union: Teamsters Local 916Location: Chicago IllinoisSalary: $50004 Annually Position Summary:Responsible for developing marketing initiatives and making presentations to promote the var...

19 days ago
Full Time

Government Affairs Specialist

Coinflip

profile Chicago - USA

Full-timeDescriptionCoinFlip is a global digital currency platform company focused on providing consumers with simple and secure access to buy and sell cryptocurrency. The company operates the worlds largest network ofcryptocurrencykiosks by transaction volume with more than 5500 kiosks across 49 U....

19 days ago
Full Time

Executive Director, Regulatory Affairs

Dyne Therapeutics

profile Waltham - USA

Company Overview:Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing c...

19 days ago
Full Time

Licensing And Regulatory Affairs Manager

Coinflip

profile Chicago - USA

Full-timeDescriptionCoinFlip is a global digital currency platform company focused on providing consumers with simple and secure access to buy and sell cryptocurrency. The company operates the worlds largest network of cryptocurrency kiosks by transaction volume with more than 5500 kiosks across 49...

19 days ago
Full Time

Regulatory Affairs Specialist 3 Multiport Da Vinci

Intuitive

profile Sunnyvale - USA

Primary Function of Position:Serve as the primary regulatory representative on project and product core teams. The Regulatory Affairs Specialist works across the organization in supporting design control activities US and Canada regulatory assessment and submissions and liaises with global regulator...

20 days ago
Full Time

Director, Regulatory Affairs And Compliance

Pilot Company

profile Knoxville - USA

This role leads and advances the enterprise compliance program strengthening the organizations culture of compliance and ensuring alignment across regulatory requirements business operations and risk management. The Director provides strategic oversight for compliance program design regulatory opera...

20 days ago
Full Time

Manager, Regulatory Affairs Strategy

Travere

profile San Diego - USA

Department:107000 RegulatoryLocation:San Diego USA- RemoteBe a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on...

21 days ago
Full Time

Head Of Global Regulatory Affairs, Oncology

Takeda

profile Boston - USA

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

21 days ago
Full Time

Senior Associate Regulatory Affairs Submission Man...

Abbvie

profile North Chicago - USA

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

22 days ago
Full Time

Senior Manager Regulatory Affairs, Global Reg Stra...

Abbvie

profile Florham Park - USA

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

22 days ago
Full Time

Senior Manager Regulatory Affairs, Global Reg Stra...

Abbvie

profile North Chicago - USA

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

22 days ago
Full Time

Remote Regulatory Affairs Contractor

Globalchannelmanagement

profile Atlanta - USA

Remote Regulatory Affairs contractor requires: Bachelors degree in engineering life sciences regulatory affairs legal or a related field 5-10 years of global medical device regulatory experience Proven experience preparing writing and submitting FDA 510k submissions (end to end) Experience with oph...

22 days ago
Full Time