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CAREERBUILDER APPLY

Full-Time | Pay: $62k - $86k/year

We have a great opportunityfor an experienced and talented Senior Regulatory Affairs Specialist to leadour international product registration projects. $62K-86K/year DOE This opportunity is perfect for you if: · YOU areRegulatory Specialist with respon...

Confidential

Signal Hill, CA

CAREERBUILDER APPLY

Full-Time | Pay: $50k - $60k/year

Safety / Regulatory Affairs Specialist Safety / Regulatory Affairs Specialist Safety / Regulatory Affairs Specialist A manufacturing company in Bristol is looking for a full-time Safety/Regulatory Specialist to oversee compliance of all safety and /or reg...

Bristol, PA

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 | Pay: $110k - $130k/year

A permanent, direct-hire Principal Regulatory Affairs Specialist job is available in San Diego, CA via Real Staffing. In this role you will participate in the review and approval process, gain insight into current FDA and international agency thinking, an...

San Diego, CA

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CAREERBUILDER APPLY

Contractor

Ref ID: 04861-9500570048 Classification: Account Executive/Staffing Manager Compensation: DOE There is an immediate opportunity for a Regulatory Affairs Specialist to support the Goleta, CA , location of a global leader in medical technology solutions. Th...

Oxnard, CA

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Full-Time

COOK MYOSITE INCORPORATED, a division of Cook Incorporated, is a growing, forward-thinking biotechnology organization seeking a full time, Regulatory Affairs Specialist to join our team. The Regulatory Affairs Specialist will provide support and knowledge...

Pittsburgh, PA

CAREERBUILDER APPLY

Full-Time | Pay: 60k - 70k /year

Regulatory Affairs Specialist (Pharmaceutical) – Irvine, CA Exciting opportunity for a Regulatory Affairs Specialist with a fully-integrated cGMP pharmaceutical development organization providing complete turn-key drug development services. Reporting into...

Irvine, CA

CAREERBUILDER APPLY

Full-Time

Position: Regulatory Affairs Specialist Location: Indianapolis, IN. Hours: 1 st shift (Monday - Friday) Summary Apex Life Sciences is searching for a Regulatory Affairs Specialist in the Indianapolis, IN. area. This is a 1 st shift full time Direct Hire o...

INDIANAPOLIS, IN

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CAREERBUILDER APPLY

Full-Time

DJO Global, Inc. is a leading global provider of high-quality, orthopedic devices, with a broad range of products used for rehabilitation, pain management and physical therapy. We also develop, manufacture and distribute a broad range of surgical reconstr...

Vista, CA

CAREERBUILDER APPLY

Full-Time

Safety/Regulatory Affairs Specialist World leading manufacturing company headquartered in Bristol, PA is seeking to fill a full-time position of Safety/Regulatory Affairs Specialist. The Safety/Regulatory Affairs Specialist will oversee compliance of all...

UCT Inc.

2731 Bartram Road
Bristol, PA

CAREERBUILDER APPLY

Contractor

Job Number: 448271 Regulatory Affairs Specialist OVERVIEW We are currently searching for a skilled professional to join a well-known client's team as a Regulatory Affairs Specialist in Swiftwater, Pennsylvania. The Regulatory Affairs Specialist will autho...

Swiftwater, PA

CAREERBUILDER APPLY

Contractor

Title: CMC-Regulatory Affairs Specialist Duration: 10 Months Contract (W2-Onsite) Location: Northbrook, IL 60062 Client: A leading pharmaceutical company Qualifications required: Bachelor’s degree in science 1-2 years in regulatory affairs CMC Good techni...

Northbrook, IL

Full-Time

The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails develop...

Globus Medical

Valley Forge Business Center
2560 General Armistead Ave.
Audubon, PA

Full-Time

A strong Scientific and technological pioneering spirit drives bioMérieux development since its creation in 1963. We design innovative in vitro diagnostic solutions for our customers that initiate new forms of scientific partnerships to be at the forefron...

St. Louis, MO

Full-Time

Requisition ID: 35501 Title: Regulatory Affairs Specialist Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports Regulatory Affairs activities for Arthrex, Inc. Essential Duties and Responsibilities: With minimal supervi...

Naples, FL

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CAREERBUILDER APPLY

Contractor

Job Title : Regulatory Affairs Specialist Location: Tewksbury, MA Duration : 1 Year Purpose of Position: Regulatory Affairs Specialist provides necessary support to regulatory affairs department in many areas including new product review, regulatory filin...

Tewksbury, MA

Full-Time

Responsibilities/Duties: • Position provides regulatory support for the SmithsMedical site based in St. Paul, Minnesota. Incumbent develop and prepareregulatory submissions, i.e., 510(k) Premarket Notification, PMA, DesignDossier, and CE Technical File...

6000 Nathan Lane North
Plymouth, MN

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CAREERBUILDER APPLY

Full-Time

Title : Regulatory Affairs Specialist Location : Barrington, IL Duration : 12 months Job Description: Regulatory Affairs Support needed as business removes artificial colors, flavors, preservatives from portfolio. Assist Regulatory Affairs team with ingre...

Barrington, IL

Full-Time

Oscor Inc. is a global US based medical device company headquartered in Palm Harbor, Florida. Oscor designs, manufactures and sells a variety of highly specialized implantable cardiac pacing leads, venous access systems and diagnostic catheters with sales...

Oscor Inc.

Palm Harbor, FL

Full-Time | Pay: $19.00 - $24.00/hour

REGULATORY AFFAIRS SPECIALIST NEEDED! Positions: 1 Position Type: Contract to Hire Pay: $19-24/hr Description: Coordinates timely preparation of requests for Certificates to Foreign Government, Certificates of manufacture, Free Sale, and Certificates of E...

Dallas, TX

CAREERBUILDER APPLY

Full-Time | Pay: $25.00 - $35.00/hour

Title: Regulatory Affairs Specialist Location: Parsippany, NJ, 07054 Duration: 06 months Responsibilities: ● Want CPG experience ● MSDS experience is always a big plus. ● Labels and operational work. ● Entry level regulatory affairs background ● Chemistry...

Parsippany-Troy Hills, NJ

CAREERBUILDER APPLY

Full-Time | Pay: 20.00 - 24.00 /hour

Kelly Services has provided outstanding employment opportunities to the most talented professionals in the marketplace. Today, we are proud to offer an excellent contract opportunity for a Regulatory Affairs Specialist with our client, a leader in the med...

Rochester, NY

Full-Time

MicroAireis a manufacturer and distributor of powered surgical instruments,sterile-packaged disposable orthopaedic accessories, SmartRelease-ECTR, PALpower-assisted liposuction, LipoFilter and Endotine bioabsorbable implants.MicroAire is a team dedica...

MicroAire Surgical Instruments, LLC

Charlottesville, VA

CAREERBUILDER APPLY

Contractor

Job Description: . Create and deliver strategic regulatory guidance for assigned projects/products. Strategies should be in alignment with global/regional positions, commercial goals, and key stakeholders/partner lines. . Manage regulatory aspects of proj...

New York, NY

CAREERBUILDER APPLY

Full-Time

This person needs to have Generic Pharmaceutical labeling experience within regulatory. JOB SUMMARY The Regulatory Affairs Associate is responsible for the generation, maintenance of Abbreviated New Drug Applications for new pharmaceutical products. This...

Somerset, NJ

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