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Full-Time

Title: Manager, Global CMC Regulatory Affairs Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting for a Manager, Global CMC Regulatory Affairs. This position will be based in Titusville, NJ, Raritan, NJ or Spring House, PA....

Spring House, PA

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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

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Full-Time

Our client, working on a potential blockbuster for dementia patients is currently seeking a Director, CMC Regulatory Affairs This job will have the following responsibilities: Primarily will be responsible for managing the CMC activities and providing reg...

New York, NY

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Contractor

I. POSITION SUMMARY: The CMC Project Planner III is responsible for supporting CMC Teams by strategically developing and maintaining Pharmaceutical Science timelines, providing evaluations of potential risks and conflicts, supporting the team on proactive...

Jersey City, NJ

CAREERBUILDER APPLY

Contractor

1 year contract opportunity with a growing pharmaceutical company in Rockville, MD! Description: This is an entry level 12 month temporary assignment in regulatory affairs, CMC position. The successful candidate must possess strong computer, communication...

Rockville, MD

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CAREERBUILDER APPLY
2w
2 weeks ago

Contractor

Duties: Provide regulatory assessment of post-approval CMC changes for assigned FDA approved NDA drug products in accordance with current FDA regulations and guidance Author and compile CMC dossiers for NDA supplements, annual reports, phase IV IND, and D...

Bridgewater, NJ

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Full-Time | Pay: $45.00 - $50.00/hour

Title: Change Control and Quality System Specialist (CMC) Location: Cambridge, MA Contract Duration: 6 months+ Our client, a pharmaceutical firm with a global footprint, is looking for looking for a candidate with a background in CMC Regulatory Affairs an...

Cambridge, MA

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Full-Time

Manager Regulatory Affairs (CMC Biologics) San Diego, CA Permanent Responsibilities: Prepare and oversee submissions with an emphasis on, but not limited to, CMC, for investigational, marketing, and/or post-licensure regulatory submissions (including INDs...

San Diego, CA

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Full-Time

Senior Director Global Regulatory Affairs CMC East San Francisco Bay Area Permanent Responsibilities: Work closely with CMC colleagues to develop CMC regulatory submission strategies, review content, and maintain submission timelines to meet business obje...

Pleasanton, CA

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2w
2 weeks ago

Full-Time/Part-Time

Regulatory CMC Manager One of our global pharmaceutical clients is currently seeking a Regulatory CMC Manager! Although we work with offices nationwide, this position is based in the King of Prussia, PA area. This is a fantastic work opportunity with comp...

King of Prussia, PA

CAREERBUILDER APPLY

Contractor

Regulatory Affairs, CMC, Manager Bachelor's degree, Life/Health Sciences preferred. Minimum of 7 years in the Pharmaceutical Industry, and a minimum 5 years regulatory cCMC experience Direct and broad experience in cross-functional CMC biopharmaceutical p...

Boston, MA

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Full-Time

Job Title : CMC Manager, Regulatory Affairs Location : South San Francisco, CA Primary Function : This CMC Manager, Regulatory Affairs position is within the Pharmaceutical Operations (PSC) group and is focused on the project and documentation management...

inVentiv Health Clinical

South San Francisco, CA

CAREERBUILDER APPLY

Full-Time

We have an immediate opening for a Director of Chemistry, Manufacturing and Controls (CMC) who will be responsible for the company’s activities for its ongoing early- and late-stage clinical trials. The successful candidate will be responsible for evaluat...

confidential

Salt Lake City, UT

Full-Time

IMPORTANT NOTE: We are very pleased to announce the location of Daiichi Sankyo, Inc.’s new US headquarters where our Parsippany- and Edison-based teams will be co-located in a combined site in early to mid-2017. Our new headquarters will be in Basking Rid...

Bernards, NJ

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Contractor

Our client, a global leader in the biopharmaceutical industry, is seeking a qualified Regulatory Affairs Specialist to join their expanding team. Responsibilities will include, but are not limited to, the following: Responsible for the development of the...

San Diego, CA

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Full-Time

IMPORTANT NOTE: We are very pleased to announce the location of Daiichi Sankyo, Inc.’s new US headquarters where our Parsippany- and Edison-based teams will be co-located in a combined site in early to mid-2017. Our new headquarters will be in Basking Rid...

Bernards, NJ

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CAREERBUILDER APPLY
4w
4 weeks ago

Contractor

One of our top clients, a leading pharmaceutical manufacturing company has multiple opportunities for a Technical Writer, CMC working in a highly motivated group located in Lexington, MA office. These opportunities are renewable contract opportunities bas...

Lexington, MA

CAREERBUILDER APPLY
4w
4 weeks ago

Full-Time

Role and Responsibilities: Essential function(s) includes, but is not limited to: Reporting to the Associate Director, the Sr. Specialist is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with glo...

Short Hills, NJ

CAREERBUILDER APPLY

Full-Time

Seeking a Technical Writer for a 4 month assignment in Lexington, MA Pay Rate : $30-35/hr Technical writing, Regulatory submissions, and MS Word/Excel required 3-5 years of experience required Perform CMC technical writing and editing assignments related...

Lexington, MA

CAREERBUILDER APPLY
2w
2 weeks ago

Contractor

Duties: Author technical documents in internal Documentum system Utilize knowledge of bacterial biologics and regulations pertaining to pre and post licensure activities related to CMC. Perform all work following applicable GMPs Work with minimal manageme...

Swiftwater, PA

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Full-Time

Job Summary This position is a frontline service position communicating to Magellan’s members and providers Magellan programs, policies, and procedures. Responsibilities include answering incoming calls on eligibility, benefits, claims, and authorization...

San Diego, CA

CAREERBUILDER APPLY

Full-Time

Sunrise System Inc. is currently seeking Associate Director Global Regulatory Development in Cambridge, MA for one of our top clients. Title: Associate Director Global Regulatory Development Location Cambridge, MA Type: Contract W2 only Duration : 12+ mon...

Cambridge, MA

CAREERBUILDER APPLY

Full-Time | Pay: $14.00 - $16.00/hour

COMMERCIAL MAINTENANCE TECHNICIAN CMC Properties is looking for a motivated and energetic Commercial Maintenance Technician to join our team at The Turfway Office Center in Florence KY. ENJOY A CAREER THAT: • Provides you with a new challenge every day •...

CMC Properties

73 Cavalier Boulevard
Florence, KY

CAREERBUILDER APPLY

Full-Time | Pay: $14.00 - $16.00/hour

COMMERCIAL MAINTENANCE TECHNICIAN CMC Properties is looking for a motivated and energetic Commercial Maintenance Technician to join our team and to be a floater among our properties along the 275 loop for KY and OH. ENJOY A CAREER THAT: • Provides you wit...

CMC Properties

Reed Hartman Drive
Cincinnati, OH

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CAREERBUILDER APPLY

Full-Time | Pay: $17.00 - $18.00/hour

For over forty years, CMC Properties has successfully owned and managed thousands of apartments, offices, and retail stores. At CMC each employee is dedicated to our core mission of Simplifying the Lives of our Customers. Whether you are a tenant, client,...

CMC Properties

717 Martin Luther King Drive West
Cincinnati, OH

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