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StartUpHire is the place to find GMP jobs. Review the list of GMP career opportunities to the left. These GMP jobs represent some of the most rewarding careers available.

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QA Compliance Specialist - Supplier QA/Materials QA

Merrimack Pharmaceuticals

QA Compliance Specialist - Supplier QA/Materials QA Quality Assurance Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of

4/28/2015  Cambridge, MA  Save This Job

Senior Director, Facilities & Engineering (15-907)

MacroGenics

Job Code: 15-907 Location: Rockville, MD Applicants must meet the following requirements: 15 years of facilities and engineering experience in a biotechnology company Previous experience with building and maintaining GMP facilities Previous experience with space planning for

4/7/2015  Rockville, MD  Save This Job

Quality Assurance Compliance Specialist- External Operations

Merrimack Pharmaceuticals

Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems

4/28/2015  Cambridge, MA  Save This Job

Pharmaceutical Quality Control Chemist

Aprecia Pharmaceuticals

Job ID40 Overview 1. Responsible for testing and release of finished products, stability samples, raw materials, registration, clinical and marketed products batches under GMP/GLP environment as per company's standard operating procedures and USP/FDA guidelines. 2. Performs

4/18/2015  East Windsor, NJ  Save This Job

Quality Assurance Specialist I, Release Coordinator

KBI Biopharma

Location: North Carolina Job Description: Responsible for release of materials for GMP manufacturing. Works directly with Warehouse personnel to release materials and resolve any compliance issues. Works directly with Manufacturing and other departments responsible for GMP

3/30/2015  Durham, NC  Save This Job

Quality Assurance Specialist I (temporary)

KBI Biopharma

Location: North Carolina Job Description: Performs compliance review for manufacturing records including batch records, solution records, equipment and part assembly records. Review manufacturing logbooks. Works directly with Manufacturing and other departments responsible for

3/30/2015  Durham, NC  Save This Job

Facilities Maintenance Technician

Merrimack Pharmaceuticals

Facilities Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of

5/28/2015  Cambridge, MA  Save This Job

Quality Control (QC) Stability Specialist

Merrimack Pharmaceuticals

Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of underlying cancer biology through its systems

5/28/2015  Cambridge, MA  Save This Job

Associate Scientist / Scientist - Upstream Cell Line Development

Merrimack Pharmaceuticals

Discovery Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding of

5/28/2015  Cambridge, MA  Save This Job

Quality Assurance Specialist, Change Control

Sagent Pharmaceuticals

Location: Schaumburg, IL, USA Department: Quality Assurance & Facility Compliance Reports To: Senior Director Quality Assurance Job Summary / Overview: Responsible for the support and approval of change controls for all internal, labeling and external changes involving our

5/21/2015  Schaumburg, IL  Save This Job

Purchasing & Materials Management Specialist (Job Code: 2015-5)

ViaCyte

Company Overview ViaCyte is a privately-held regenerative medicine company focused on developing a novel cell therapy for the treatment of diabetes. ViaCyte?s lead product candidate, the VC-01 combination product, is based on the production of pancreatic progenitor cells derived

5/20/2015  San Diego, CA  Save This Job

Scientist/Senior Scientist Product Development

Aprecia Pharmaceuticals

Job ID38 OverviewThe Sr Product Development Scientist will have a high degree of technical and mechanical insight, experience in troubleshooting and tech transfer, and act as a liaison to the Tech Sending Group. He/She will also be responsible for pre-formulation, formulation,

5/18/2015  East Windsor, NJ  Save This Job

Facilities Project Engineer

Aprecia Pharmaceuticals

Job ID50 OverviewThe Project Engineer position?s primary responsibility is the administrative operation and troubleshooting of the Building Automation System (BAS) and facility support systems at the Aprecia Blue Ash facility to comply with GXP standards and maintain the systems

5/18/2015  East Windsor, NJ  Save This Job

R&D Quality Assurance Manager

Corium International

Menlo Park, CA Major Responsibilities This position is primarily responsible for Quality Assurance activities to support R&D development projects - including clinical and preclinical studies. This position will mainly be focused in supporting cGMP activities and projects and may

5/14/2015  Menlo Park, CA  Save This Job

Supervisor, Manufacturing (External Control)

T2 Biosystems, Inc.

Stage 2: Product Development 

Tracking Code 117-093 Job Description The successful candidate will be responsible for supervising External Control and Verification Panel Manufacturing process from material receipts through shipments including, but not limited to: production scheduling, inventory control,

5/5/2015  Lexington, MA  Save This Job

Validation Engineer

Merrimack Pharmaceuticals

Validation Engineer Manufacturing Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper

4/28/2015  Cambridge, MA  Save This Job

Senior Validation Engineer

Argos Therapeutics

ARGOS IS GROWING! After having met several important milestones including exciting clinical data, we are poised for new strategic objectives which will require significant new resources. Those new resources include a well-qualified Senior Validation Engineer. SCOPE: Prepare,

4/18/2015  Durham, NC  Save This Job

Supply Chain Associate (14-177)

FibroGen

Job Location: San Francisco, CA Description: Supply Chain Associates are tasked with providing support to managers in transferring the Clinical Trial Material (CTM) from manufacturers to the Clinical Research Organization (CRO) and sites. The successful incumbent will plan and

4/15/2015  San Francisco, CA  Save This Job

QA Specialist II (15-519)

MacroGenics

Job Code: 15-519 Location: Rockville, MD Applicants must meet the following requirements: Bachelor?s degree with a minimum of two to five years experience working in a biotech GMP manufacturing facility - previous GMP and auditing experience required Must be able to solve

4/7/2015  Rockville, MD  Save This Job

Director Quality

Inotek Pharmaceuticals

Position Summary Reporting to the Chief Scientific Officer, this person is responsible for establishing and leading the strategic direction of Quality for the Company. The successful candidate will ensure that robust quality procedures and systems are developed and maintained to

3/30/2015  Lexington, MA  Save This Job