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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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Process Engineer, Cell Culture

Acceleron Pharma

Process Engineer, Cell Culture? Help Please fill in the information below and use the navigational buttons to continue. Warning: Using your browser's Back and Forward buttons may produce undesirable results. Process Engineer, Cell Culture About Acceleron: Acceleron is a

12/27/2016  Cambridge, MA  Save This Job

Associate Director, Quality Control

Argos Therapeutics

Description This is an exciting time to be joining Argos Therapeutics, an RTP-based biopharmaceutical company focused on the development and commercialization of individualized immunotherapies for the treatment of cancer and infectious diseases. This is a critical time for the

1/31/2017  Durham, NC  Save This Job

Experienced Scientist/Engineer

Acceleron Pharma

Experienced Scientist/Engineer, Purification Process Development? Help Please fill in the information below and use the navigational buttons to continue. Warning: Using your browser's Back and Forward buttons may produce undesirable results. Experienced Scientist/Engineer,

1/26/2017  Cambridge, MA  Save This Job

Director, Validation

T2 Biosystems, Inc.

Stage 2: Product Development 

Tracking Code 305-093 Job Description The Director, Validation will report directly to the Vice President, Manufacturing, and will provide hands-on technical support and leadership for the validation of manufacturing processes, equipment, infrastructure and systems.

1/23/2017  Lexington, MA  Save This Job

Specialist, Quality Systems

Sagent Pharmaceuticals

uApplication Deadline: February 28, 2017 Location: Schaumburg, Illinois, USA Job Overview: Provide Quality Assurance support for lifecycle management of products marketed by Sagent. Proactively support the existing quality systems as necessary including writing policies and

2/8/2017  Schaumburg, IL  Save This Job

Manufacturing Associate II

Argos Therapeutics

Description The individual will be primarily responsible for production of autologous cell-based immunotherapy products to support clinical and commercial operations. In addition, the individual will be responsible for clean room routines, operating equipment, recording and

1/31/2017  Durham, NC  Save This Job

Senior QC Analyst

FibroGen

FibroGen seeks a highly skilled Senior QC Analyst or QC Specialist to run primarily chromatographic assays (HPLC and GC) in our San Francisco GMP laboratory to support product release and on-going stability. Responsibilities: The incumbent will perform analytical testing of

1/30/2017  San Francisco, CA  Save This Job

Senior Director of Quality Assurance

Ardelyx

Quality Assurance Fremont, California Apply Description Sr. Director, Quality Assurance Ardelyx is building an integrated biopharmaceutical company with a gastrointestinal and cardio-renal focus. Our mission is to serve patients through the discovery, development and

1/16/2017  Fremont, CA  Save This Job

Sr. Engineer, Manufacturing Sciences-Upstream #562

KBI Biopharma

Location: North Carolina Job Description: The successful candidate will apply scientific and engineering principles to successfully enroll new biopharmaceutical processes into the cGMP manufacturing facility. The scope of this role includes: Acting as the technical transfer lead

12/21/2016  Durham, NC  Save This Job

Facilities Engineering Coordinator #204

KBI Biopharma

Location: Colorado Job Description: Coordinate routine and corrective work with the manufacturing operations Scheduler/Planner to support work within a GMP manufacturing environment. Manage work order work flow within ?Blue Mountain? KBI?s computerized maintenance management

12/21/2016  Boulder, CO  Save This Job

Sr. Engineer, Manufacturing Sciences #559

KBI Biopharma

Location: North Carolina Job Description: The successful candidate will apply scientific and engineering principles to successfully enroll new biopharmaceutical processes into the cGMP manufacturing facility. The scope of this role includes: Acting as the technical transfer lead

12/21/2016  Durham, NC  Save This Job

QA Specialist II #195

KBI Biopharma

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 development

12/21/2016  Boulder, CO  Save This Job

Manager/Sr. Manager Supply Chain

Ardelyx

CMC Fremont, California Apply Description Manager/Sr. Manager, Supply Chain Management Ardelyx is building an integrated biopharmaceutical company with a gastrointestinal and cardio-renal focus. Our mission is to serve patients through the discovery, development and

2/15/2017  Fremont, CA  Save This Job

Quality Control Inspector

K2M

Location: Corporate Office - Leesburg, VA Full Time Requisition Number: req339 Summary The purpose of this position is to ensure that all purchased, in-process, and completed product is manufactured within specifications regarding configuration, dimension, aesthetics,

2/9/2017  Leesburg, VA  Save This Job

Manager, Quality Assurance

Ardelyx

Quality Assurance Fremont, California Apply Description Manager, Quality Assurance Ardelyx is building an integrated biopharmaceutical company with a gastrointestinal and cardio-renal focus. Our mission is to serve patients through the discovery, development and

1/16/2017  Fremont, CA  Save This Job

Specialist, Quality

Sagent Pharmaceuticals

Application Deadline: October 31, 2016 Location: Schaumburg, Illinois, USA Job Summary / Overview: Responsible for the execution of batch record reviews and associated product quality issue resolution. Authorizes shipments from Sagent?s contract manufacturing organizations

1/9/2017  Schaumburg, IL  Save This Job

Associate Director/Director CMC, Regulatory Affairs

FibroGen

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.

12/31/2016  San Francisco, CA  Save This Job

Quality Assurance Associate

Acceleron Pharma

Quality Assurance Associate About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of innovative therapeutics to treat serious and rare diseases. Its pioneering research platform leverages the

12/27/2016  Cambridge, MA  Save This Job

Quality Control Associate -Temp to Perm

T2 Biosystems, Inc.

Stage 2: Product Development 

Tracking Code 285-093 Job Description We are seeking a talented and highly motivated individual to join our team as a Quality Control Associate. This position reports to the Senior Director, Quality Control and is a temp to perm position. Required Skills B.S. science related

12/24/2016  Lexington, MA  Save This Job

Quality Assurance Specialist III/Sr. Quality Assurance Specialist

MacroGenics

Requisition Number 17-902 Category Quality Assurance Job Location US-MD-Rockville Type Regular Full-Time More information about this job Overview MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based

1/25/2017  Rockville, MD  Save This Job