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Nodality, selected as the ?Most Promising Company? at the 2011 Personalized World Medicine Conference, is looking for an individual who is motivated to apply his/her bioinformatics and computer science skills to the high-impact area of personalized medicine. Our expertise in4/10/2013 San Francisco, CA Save This Job
Applicants must meet the following requirements: Bachelor?s or more advanced degree in biochemistry, chemical engineering or related scientific discipline; additional education in management a plus Ten years relevant industry experience in a process development or manufacturing4/9/2013 Rockville, MD Save This Job
OBJECTIVES: Effectively manage Contract Manufacturing and Quality Control testing laboratories in support of GMP manufacturing. This objective includes method and process transfer, validation, manufacturing, testing, release and distribution of vaccine products. Provide QA5/6/2013 Bozeman, MT Save This Job
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 several Manufacturing Associates. OVERVIEW: Argos Therapeutics,4/21/2013 Durham, NC Save This Job
Quality Assurance Compliance Specialist is responsible for conducting routine reviews and audits of documents and data to ensure compliance with Standard Operating Procedures (SOPs), protocols, and applicable regulations, including current Good Manufacturing Practices, Good4/2/2013 Cranbury, NJ Save This Job
Reports To: President and CEO Description: This position is responsible for developing and carrying out Avid?s quality assurance and compliance programs in support of medical imaging drug development and of commercial manufacturing (USA and International). The individual works3/25/2013 Philadelphia, PA Save This Job
Description: FibroGen seeks a QA Director / Associate Director to support the manufacture of Drug Substance and Drug Products at Contract Manufacturing Organizations (CMOs) to ensure that FibroGen?s drugs are in compliance with Good Manufacturing Practices (GMP) and are of the4/16/2013 San Francisco, CA Save This Job
Merrimack Pharmaceuticals is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of serious diseases, with an initial focus on cancer. Merrimack applies Network Biology, its5/15/2013 Cambridge, MA Save This Job
Applicants must meet the following requirements: Bachelor?s or Masters degree in the life sciences or equivalent discipline Minimum 1 ? 5 years of GMP manufacturing or process development experience Working knowledge of GMP?s is strongly preferred, experience with laboratory5/9/2013 Rockville, MD Save This Job
The purpose of this position is to ensure that all purchased, in-process, and completed product is manufactured within specifications regarding configuration, dimension, aesthetics, contamination, surface finish, packaging/ labeling, and material properties to meet the company?s4/24/2013 Malvern, PA Save This Job
Shift Times: M-F Shift 1: 6am-2:30pm M-F Shift 2: 2pm-10:30pm M-F Shift 3: 10pm-6:30am Nanosys is looking for several Production Chemists who will be responsible for supporting the group?s production of quantum dots including performing distillations and synthetic chemistry4/22/2013 Palo Alto, CA Save This Job
Major Responsibilities Provide technical machine maintenance and leadership support to overall reliability of manufacturing equipment. Prepare and set up machinery for scheduled production runs. Provide expertise and guidance for equipment modifications, repairs, upgrades, and4/16/2013 Grand Rapids, MI Save This Job
Job Summary The ideal AD, Quality Assurance candidate is a technical savvy quality professional with prior management experience. This position is responsible for a number of key quality systems and close oversight of CMOs. The job requires up to 10% travel, excellent4/9/2013 Palo Alto, CA Save This Job
Tracking Code 1797 Job Description JOB OBJECTIVE: Manage and perform the Process Validation activities for all manufacturing facilities, equipment, processes, and critical utilities. ESSENTIAL DUTIES: 1. Work with the Operations Engineering and validation Team to produce3/30/2013 Madison, WI Save This Job
DEPARTMENT: Pharmaceutical Operations Relypsa will soon be located in Redwood City and we are hiring! We are seeking a reliable, self-motivated professional for the position for a Scientist level in the Analytical Development Group supporting late stage drug development3/25/2013 Santa Clara, CA Save This Job
The purpose of this position is to ensure that all purchased, in-process, and completed product is manufactured within specifications regarding configuration, dimension, aesthetics, contamination, surface finish, packaging/ labeling, and material properties to meet the company?s3/25/2013 Malvern, PA Save This Job
COMPANY DESCRIPTION Liquidia Technologies is a privately-held clinical stage company focused on advancing vaccines and therapeutics that leverage the PRINTtechnology for design and manufacture of engineered particles. The PRINTtechnology offers unprecedented control of particle3/23/2013 Research Triangle Park, NC Save This Job
Department: Regulatory Affairs Classification: Exempt Reports To: Associate Director Regulatory Affairs Job Summary / Overview: This role is primarily responsible for managing the development of labeling and managing key labeling systems and processes to support labeling3/19/2013 Schaumburg, IL Save This Job
OpGen, Inc. is a leading innovator in rapid, accurate genomic and DNA analysis systems and services. The company has developed a platform, The Argus Whole Genome Mapping System and also offers MapIt? Services that provide high resolution, whole genome restriction maps for3/18/2013 GAITHERSBURG, MD Save This Job
Job Summary: The Assembler is responsible for the assembly, inspection and test of Ikoniscope instruments in accordance with the quality goals, cost targets and the production schedule. Job Functions and Responsibilities Will assemble instruments in a timely manner to meet3/17/2013 New Haven, CT Save This Job