19 Pharmaceutical Quality Control Jobs in Burlington, MA
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Cleaning 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 5-8 years of validation experience in pharmaceutical, medical 6 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 23 days ago
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Quality Assurance Associate I Cambridge Isotope Laboratories, Inc. - Tewksbury, MA for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment. Responsibilities Maintenance and management of CIL’s change control 17 days ago
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QC Chemist TalentBurst, an Inc 5000 company - Framingham, MA, United States The Quality Control department supports the Seprafilm (medical device) and Sodium Hyaluronate (active pharmaceutical ingredient) GMP operations at the 74/76 NYA Manufacturing Facility. The department 8 days ago
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Sr. Cleaning 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 30 days ago
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Senior Quality Engineer I Werfen - Bedford, Massachusetts , including R&D, quality control, manufacturing and design engineering Understanding of the application of technical principles and engineering problem solving to resolve complex issues. ASQ Quality Engineering 16 days ago
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QA Head Sun Pharma - Billerica, Massachusetts, USA to us. Manage the development, establishment, and maintenance of Quality Systems, policies, processes, procedures and controls ensuring that performance and quality of cGMP documentation and records 29 days ago
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Quality Control Documentation Specialist Cambridge Isotope Laboratories, Inc. - Tewksbury, MA that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Documentation Specialist More than 30 days ago
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Senior Manager, Regulatory CMC Lead Biogen - Cambridge, Massachusetts at least 3 years of experience in Regulatory CMC and preferably 2 years professional experience in pharmaceutical manufacturing, analytical development, or quality assurance/control or related technical 9 days ago
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Quality Control Laboratory Support Technician Cambridge Isotope Laboratories, Inc. - Andover, MA that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Laboratory Support More than 30 days ago
Top locations
- Tewksbury, MA (5)
- Andover, MA (4)
- Boston, MA (4)
- Worcester, MA (4)
- Bedford, MA (3)
- Westborough, MA (3)
- Billerica, MA (2)
- Framingham, MA (2)
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