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The Pharmaceutical Development department at Calithera Biosciences is seeking a highly motivated individual to lead Drug Product development and manufacturing of small molecule oncologic agents. Candidates should have strong background in oral solid dose formulation development,7/5/2016 South San Francisco, CA Save This Job
Calithera Biosciences is seeking a highly motivated individual to support our clinical and pre-clinical small molecule oncology programs. Candidates should have strong analytical chemistry skills, with particular emphasis on HPLC method development and problem solving. Knowledge7/5/2016 South San Francisco, CA Save This Job
Application Deadline: August 31, 2016 Location: Schaumburg, IL Job Summary / Overview: Responsible for oversight of all labeling related systems and processes supporting the pre and post ANDA filing process and commercially marketed products, as well as manage track-and-track8/19/2016 Schaumburg, IL Save This Job
Requisition Number: 16-703 Job Title: QC Analyst II/III - Analytical City: Rockville State: MD QC Analyst II/III - Analytical Apply Now Email Description/Job Summary MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next8/3/2016 Rockville, MD Save This Job
Location: Colorado Job Description: Performs compliance review on the following records: batch record (includes on-the-floor review of records); release data. Reviews and approves Master Batch Records and Solution Records. Works directly with manufacturing, the laboratory and8/1/2016 Boulder, CO Save This Job
Location: Colorado Job Description: Performs compliance review on the following records: batch record/formulation record (includes on-the-floor review of records); release and stability data, method qualification/validation reports, stability protocols and development8/1/2016 Boulder, CO Save This Job
Location: North Carolina Job Description: Leads and directs the Quality Engineering group supporting GMP manufacturing of bulk drug substance (Biologics). Implements, improves, and functions as the owner of the QA-on-the-floor inspection program. Ensures QA oversight of on-going8/1/2016 Durham, NC Save This Job
Apply Now Email Description/Job Summary MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 200+ dedicated individuals is advancing a pipeline of product candidates to treat7/4/2016 Rockville, MD Save This Job
Company A R&D firm that produces purified human milk oligosaccharide treatment products, research milk bioactive compounds in human milk, such as stem cells, probiotics, and antibodies. Responsibilities ? Develop new methods using High Performance Anion Exchange with8/31/2016 City of Industry, CA Save This Job
Position Description: Responsible for leading the CMC RA function within the RA department, The Associate Director or Director will provide CMC regulatory guidance on CMC requirements for investigational l compounds in the development phase through marketing registration.8/10/2016 San Francisco, CA Save This Job
FibroGen seeks a highly qualified and motivated Senior QC Release Analyst for Document Review of our leading compound, Roxadustat. Roxadustat is a small molecule in Global Phase 3 studies for treatment of anemia in Chronic Kidney Disease (CKD). Primary duties include: The8/10/2016 San Francisco, CA Save This Job
COMPANY WORKING AT GENOCEAASSOC. DIRECTOR / DIRECTOR OF QUALITY ASSURANCE Position Summary The Associate Director/Director of Quality Assurance manages the development and oversight of our Quality Management System and supports the GCP, GLP and GMP activities (both internal and7/3/2016 Cambridge, MA Save This Job
Job Location Tucson, Arizona Essential Duties Provide technical leadership in manufacturing process development / improvement and sustaining Document manufacturing processes through Work Instructions Determine changes for Process / yield improvements Complete Failure Analysis7/2/2016 Tucson, AZ Save This Job
Associate Director of Quality Control About Us Associate Director of Quality Control Scope This is an exciting time to be joining Argos Therapeutics, an RTP-based biopharmaceutical company focused on the development and commercialization of individualized immunotherapies for8/11/2016 Durham, NC Save This Job
Prolacta Bioscience Inc. ? City of Industry, CA Posted 21 days ago Apply Now Email Job Save Job Job Snapshot Full-Time Experience - At least 1 year(s) Degree - High School Biotechnology Manufacturing 53 Applicants How Do You Compare to the Competition? Get facts about8/31/2016 City of Industry, CA Save This Job
About Enanta Enanta Pharmaceuticals is a research and development-focused biotechnology company that uses its robust chemistry-driven approach and drug discovery capabilities to create small molecule drugs for viral infections and liver diseases. Enanta?s research and development8/30/2016 Watertown, MA Save This Job
Location:Methuen, MA Job Code:QCIDT0816 Description The QC Inspector will be responsible for inspecting materials and products for conformance to specifications using fixed or pre-set measuring instruments. Ensures materials and products are in accordance with established8/25/2016 Methuen, MA Save This Job
Location:Methuen, MA Job Code:PTDT0816 Description The Production Technician is responsible for assembling electro-mechanical medical devices that are in compliance with applicable FDA, state, OSHA, and ISO regulations and standards. The job requires the individual to be a team8/25/2016 Methuen, MA Save This Job
Location:Methuen, MA Job Code:EMETDT0816 Description Our rapidly growing medical robotics division is searching for enthusiastic engineers wanting to make a difference. We develop medical robots by working with top surgeons and a cross-functional engineering team. This person8/25/2016 Methuen, MA Save This Job
Validation Engineer - CONTRACT 3-6 months Billerica, MA Apply View All Jobs Share This Job Job Description VALIDATION ENGINEERING PROJECT SUMMARY: The Validation Engineering CONTRACTOR will be responsible for creating and executing process and equipment validations.8/11/2016 Billerica, MA Save This Job