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CAREERBUILDER APPLY
1w
1 week ago

Full-Time

Regulatory Affairs I/II/III (All Shifts) Leading pharmaceutical company in rapid growth mode is currently seeking Regulatory Affairs candidates at ALL LEVELS and SHIFTS to work within Regulatory Operations, Labeling, Packaging and CMC. New Grads and Exper...

Novato, CA

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CAREERBUILDER APPLY
3d
3 days ago

Full-Time

Vaco has an exciting new client that has an immediate opportunity for a Regulatory Affairs Specialist in Memphis, TN. In this role you will be responsible for maintaining the company's quality system and ensuring compliance with ISO 13485 and FDA regulati...

Germantown, TN

CAREERBUILDER APPLY

Full-Time

In March 2016, we spun off from our previous parent company and became our own publicly traded company called Nuvectra! We're a medical device company specializing in the neuromodulation / pain management space. We have some very exciting things taking pl...

10675 Naples Street Northeast
Minneapolis, MN

CAREERBUILDER APPLY

Full-Time | Pay: $65k - $75k/year

Are you an organized senior-level tech writer with working knowledge of regulatory requirements? The Regulatory Affairs Technical Writer position is a direct-hire opportunity with one of our clients in RTP, NC. Target salary range is $65,000 - $75,000 wit...

Morrisville, NC

CAREERBUILDER APPLY
2d
2 days ago

Full-Time

Regulatory Affairs Associate at MAGNUS Personnel Corporation Empower Your People… Magnus Personnel partners with the World’s most respected and intelligent companies to help them identify talented, smart people like you. We build the careers of high perfo...

Magnus

Orange County, CA

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CAREERBUILDER APPLY

Full-Time

My client, an foreign pharmaceutical establishing US presence, is seeking a Regulatory Affairs Consultant on a contract-to-hire basis. This Regulatory Consultant will be their first hire in Regulatory, and will be supported/working with two Clinical Proje...

Princeton, NJ

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CAREERBUILDER APPLY
2w
2 weeks ago

Full-Time

Summary: Provide quality systems, regulatory and technical product support for internal and external customer requests. Ensure that company products comply with all of the government regulations and laws and religious dietary laws pertaining to the manufa...

Kalamazoo, MI

CAREERBUILDER APPLY

Full-Time | Pay: $175k - $225k/year

This position is open as of 4/27/2017. Director, Regulatory Affairs - Help Cure Cancer! Based in the bustling environment of New York City, we are a publicly traded pharmaceutical company that is revolutionizing the therapeutic world. Utilizing the newest...

Princeton, NJ

Full-Time | Pay: $60k - $100k/year

Regulatory Affairs Specialist- The Regulatory Affairs Senior Specialist executes the pharmaceutical regulatory strategies for assigned products. Supports the Regulatory Affairs Senior Manager with regard to submissions and other product development and su...

Bridgewater, NJ

CAREERBUILDER APPLY

Full-Time

Main purpose of the Senior Regulatory Affairs Specialist: This position provides support in the company ensuring compliance with all applicable regulatory requirements with specific focus on product listings, site registrations, state licensing, and marke...

San Antonio, TX

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Full-Time

Overview: The Company Kemin Industries Inc. is a global company headquartered in Des Moines, Iowa, USA. Kemin (www.kemin.com) provides “inspired molecular solutions” specifically developed to provide nutrition and health benefits for humans and animals. C...

Des Moines, IA

CAREERBUILDER APPLY

Full-Time

Specialist, Regulatory Affairs in Rensselaer, NY Albany Molecular Research Inc. provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Regulatory Affairs Specialist is a member of the Regulator...

Rensselaer, NY

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Full-Time | Pay: $120k/year

Our client is currently seeking a Regulatory Affairs Manager. Salary/Hourly Rate: Up to $120K DOE Responsibilities: The Manger, Regulator Affairs, will review and manage submitting eCTD submissions for generic and new drug development projects and markete...

New Providence, NJ

CAREERBUILDER APPLY

Full-Time

First Quality Enterprises, Inc. (FQE), founded in 1988, is a global multi-billion dollar privately held company with nearly 5,000 employees. FQE's corporate offices are located in Great Neck, New York, with manufacturing facilities and offices in Pennsylv...

Lock Haven, PA

CAREERBUILDER APPLY

Full-Time

Job Title: Regulatory Affairs Associate This position may be structured under a consulting or independent contractor status or an as needed arrangement. Job Description: The Regulatory Affairs Associate will be responsible for research and opinion on regu...

10 Westbury Parkway
Bluffton, SC

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CAREERBUILDER APPLY

Full-Time

Description: The client is seeking an experienced Regulatory Affairs professional with a solid understanding of the regulatory submissions and drug development processes. IND/NDA submissions experience is critical for this FT, Princeton-based position. Ca...

Princeton, NJ

CAREERBUILDER APPLY

Full-Time

Kelly Services is looking for a Senior level Regulatory Affairs Specialist in Mounds View, MN POSITION DESCRIPTION : The Principal Regulatory Affairs Specialist is responsible for coordinating and preparing submissions related to our medical devices inclu...

Mounds View, MN

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Full-Time

Regulatory Affairs, Group Manager The Group Manager, US Regulatory, is responsible for preparing, filing and gaining approval of 510(k), IDE, and PMA submissions to the U.S. Food and Drug Administration (FDA) for class II and class III products. This posi...

Valley Forge Business Center
Audubon, PA

CAREERBUILDER APPLY

Full-Time

Job Req # 521375 Global Pharmaceutical Company is looking for: POSITION: Regulatory Affairs Associate LOCATION: West Caldwell, New Jersey DEGREE: Required EXPERIENCE: 2+ Years experience in Pharmaceutical regulatory affairs including writing ANDA, NDA, an...

West Caldwell, NJ

CAREERBUILDER APPLY

Full-Time

Empower Your People… Magnus Personnel partners with the World’s most respected and intelligent companies to help them identify talented, smart people like you. We build the careers of high performance professionals over the long term with North America's...

Magnus

Pomona, CA

CAREERBUILDER APPLY

Full-Time

Associate Manager Regulatory Affairs Irvine, CA Permanent The Associate Manager Regulatory Affairs will focus on supporting US and EU clinical and commercialization strategies and submissions. Looking for a diligent RA professional who works well across f...

Irvine, CA

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CAREERBUILDER APPLY

Full-Time

Apex Life Sciences has an immediate Direct Hire opening for a Director of Regulatory Affairs for a leading client in the Greater Philadelphia Region! Reporting to the Executive Director (ED), the Director of Regulatory Affairs (DRA) performs the following...

philadelphia, PA

CAREERBUILDER APPLY

Full-Time | Pay: $70k - $85k/year

Our growing pharmaceutical client is currently seeking Regulatory Affairs Associates! Job Title: Regulatory Affairs Associate Location: West Caldwell, NJ Duration: PERMANENT Responsibilities include: Independently prepares, reviews and submits high qualit...

West Caldwell, NJ

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CAREERBUILDER APPLY

Contractor

Regulatory Affairs- You will play an integral role in bringing new products to market. Once marketed, the products must be maintained in full compliance to local regulations. Regulatory Affairs has a key role to play in ensuring that Our Clients products...

Glenview, IL

Full-Time

Regulatory Affairs Technician PURPOSE OF THE POSITION The primary purpose for this position is to support key areas of vast and expanding regulatory affairs needs in Post Approval product maintenance and approvability. KEY RESPONSIBILITIES Maintains curre...

Bimeda Inc

Le Sueur, MN

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