22 Pharmaceutical Quality Control Jobs in Cambridge, MA
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Supervisor, Quality Control Operations Editas Medicine - Cambridge, MA, United States of Quality Control experience in the Biotech and/or Pharmaceutical industry, or Masters Degree with 5+ years in Biology or other science related filed. GMP experience a Must. The ideal candidate will be well 6 days ago
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Supervisor of QC Ops - 2481 Editas Medicine - Cambridge, Massachusetts of Quality Control experience in the Biotech and/or Pharmaceutical industry, or Masters Degree with 5+ years in Biology or other science related filed. GMP experience a Must. The ideal candidate will be well 8 days ago
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Program Manager Apex Systems - Lexington, MA, United States to pharmaceutical manufacturing regulations and quality assurance/control Master's degree or equivalent 4 days ago
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Director of Quality Assurance Life Sciences Recruitment - Lexington, MA, United States procedures for GMP manufacturing of clinical materials. Implementing quality systems such as deviation management, CAPA, and change control. Preparing for and managing regulatory inspections and external 21 days ago
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QC Microbiologist ProClinical - Cambridge, MA Quality Control experience in a cGMP organization with a focus in Microbiology. Knowledge of GMP, microbiology, aseptic technique, and general laboratory instrumentation is preferred. Experience in lab 7 days ago
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Molecular Biology Quality Control Analyst I Tandym Group - Woburn, MA, United States A leader in the pharmaceutical industry is seeking a Quality Control Analyst I to join their team. In this role, the Molecular Biology Quality Control Analyst I will be responsible for supporting 12 days ago
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System Administrator (Apps focused / Pharmaceutical Industry) Robert Half - Billerica, MA, United States -Focused Systems Administrator, you will play a pivotal role in managing day-to-day system administration, user support, and implementation of GxP Computerized Systems in their Quality Control Analytical Lab 8 days ago
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QC Microbiology Associate Yoh - Cambridge, MA in a relevant scientific discipline or 2-5 years Quality Control experience in a cGMP organization with a focus in Microbiology. Shift: Monday through Friday, 1st shift (9 am to 5 pm) ***PLEASE NOTE: PARKING 8 days ago
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Senior Validation Specialist (Contract) a Medical Device Equipment located in near Lexington, MA - Lexington, MA, United States validation input for quality systems such as CAPAs and change controls. Undertake other assigned duties and projects. Qualifications: Minimum 8-10 years of validation experience in pharmaceutical, medical 16 days ago
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Senior Validation Engineer a Medical Devices company in MA - Bedford, MA, United States calibration or validation. Initiating and/or providing validation input on quality systems such as CAPAs and change controls. Responsible for other duties and projects as assigned. RESPONSIBILITIES Minimum 8 15 days ago
Top locations
- Andover, MA (6)
- Tewksbury, MA (6)
- Worcester, MA (4)
- Framingham, MA (3)
- Lexington, MA (3)
- Bedford, MA (2)
- Billerica, MA (2)
- Boston, MA (2)
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