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GMP Jobs

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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Quality Assurance Manager

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

2/17/2015  Cambridge, MA  Save This Job

Associate Director, Facility Compliance

Sagent Pharmaceuticals

Location: Schaumburg, Illinois Associate Director Facility Compliance Department: Quality Assurance & Facility Compliance Reports To: Corporate Vice President, Global Quality Assurance & Facility Compliance Job Summary / Overview: Ensure Sagent has a robust FDA defendable

3/12/2015  Schaumburg, UT  Save This Job

Quality Assurance Senior Specialist, Exceptions Coordinator

KBI Biopharma

Location: North Carolina Job Description: Works directly with Manufacturing and other departments responsible for GMP activities to resolve production related deviations and other compliance issues in a timely manner. Generates metrics, trends an project specific status updates

2/23/2015  Durham, NC  Save This Job

Quality Assurance Specialist

Sagent Pharmaceuticals

Application Deadline: March 31, 2015 Location: Schaumburg, IL, USA Department: Quality Assurance & Facility Compliance Reports To: Director Quality Assurance or Quality Assurance Supervisor Job Summary / Overview: Responsible for the support and guidance of new product

3/12/2015  Schaumburg, IL  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

3/4/2015  East Windsor, NJ  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

2/23/2015  Durham, NC  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

2/23/2015  Durham, NC  Save This Job

Manufacturing Associate

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

2/17/2015  Cambridge, MA  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

2/17/2015  Cambridge, MA  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

3/25/2015  Lexington, MA  Save This Job

QA Documentation Specialist

Merrimack Pharmaceuticals

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 cancer. Merrimack seeks to gain a deeper understanding of

3/19/2015  Cambridge, MA  Save This Job

Staff Scientist I, Quality Control

Relypsa

SUMMARY: Work as part of a team in the identification and resolution of CMC method related issues. Evaluate, and implement novel and viable analytical technologies for characterization of polymers. Conduct method transfer between contract service providers. Assist in protocol

3/16/2015  Redwood City, CA  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

3/4/2015  San Francisco, CA  Save This Job

Sr. Scientist

Aprecia Pharmaceuticals

Job ID39 OverviewConduct the pre-formulation, formulation, and process development aspects of pharmaceutical dosage form development projects (as either an individual contributor or technical leader of junior scientists) using Aprecia?s proprietary technology. May supervise and

3/4/2015  East Windsor, NJ  Save This Job

Process Engineer/Product Development Scientist

Aprecia Pharmaceuticals

Job ID38 OverviewThe Sr Product Development Scientist will perform tech transfer, troubleshooting and act as a liaison to the Tech Sending Group, in addition to responsibilities in pre-formulation, formulation, and process development aspects of pharmaceutical dosage form

3/4/2015  East Windsor, NJ  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,

3/4/2015  Durham, NC  Save This Job

QC Analyst (Environmental Monitoring) (15-902)

MacroGenics

Job Code: 15-902 Location: Rockville, MD Applicants must meet the following requirements: Bachelors/Masters Degree in scientific discipline or equivalent. 1 to 2 years related experience with a Bachelors Degree or no experience with a Masters Degree. Working knowledge of

2/25/2015  Rockville, MD  Save This Job

Senior Quality Assurance Specialist, Facilities

KBI Biopharma

Location: North Carolina Job Description: Manages the change control system. Works directly with functional areas to review and approve change controls. Works to continuously improve and streamline the change control system. Supports Facility Engineering. Performs review and

2/23/2015  Durham, NC  Save This Job

Quality Systems Manager

Prolacta Bioscience

Department(s) Quality Management Reports to Director of Quality Company Prolacta is the pioneer in human milk-based nutritional products for premature infants in the neonatal intensive care unit (NICU). Prolacta believes that there is no adequate replacement for human breast milk

2/23/2015  City of Industry, CA  Save This Job

Research Associate III/ Senior Research Associate

Relypsa

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a

2/14/2015  Redwood City, CA  Save This Job