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Supervisor, QC Analytical

United States, Bedford · Job Posted February 20, 2026
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Job Description

The QC Analytical Supervisor will have responsibility for supporting all activities in the Quality Control Laboratory including completing the majority of the peer review in the department and approving the majority of procedures used in the analytical department. The work includes the testing of in-process samples, finished product samples and raw materials. The QC Analytical Supervisor will communicate with clients regarding Out of Specification and other Quality System Events. The person in this position has knowledge of commonly-used analytic concepts, practices, and procedures within the field of his/her responsibilities. Also, must be familiar with cGMPs as they relate to analytical test methodologies and practices.

Job Responsibility

  • Prioritize and distribute work to the analysts working in the QC Analytical laboratory
  • Conduct OOS and customer complaint investigations
  • Complete peer review of work executed within the analytical laboratory
  • Train new Employees
  • Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing
  • Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation as required
  • Perform instrument calibrations and preventative maintenance as needed
  • Documents laboratory work using laboratory worksheets/notebooks. Documentation must be detailed and meet CGMP requirements
  • Write, review and revise SOPs as required
  • Other duties as assigned or required

Requirements

  • 5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
  • Experience working in a cGMP laboratory required
  • Experience working in a CMO (contact manufacturing/development organization) preferred
  • Prior leadership experience is preferred
  • Bachelor of Science in a scientific area of study
  • Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
  • Ability to prioritize tasks for staff
  • Ability to make informed decisions
  • Detail oriented
  • Strong oral and written communication skills
  • Excellent organization skills
  • Office Suite experience (Excel, Word, Access, and PowerPoint)
  • Excellent interpersonal skills and the ability to communicate well both orally and in in writing
  • Ability to multi-task in a dynamic environment with changing priorities
  • Resilient, can quickly move forward despite challenges
  • A drive to achieve results for self, and the team, and is cable of working with limited supervision
  • Positive attitude and strong team, cross team collaboration
  • Honesty, integrity, respect and courtesy with leadership and peers
  • Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services

Nice to have

  • Experience working in a CMO (contact manufacturing/development organization)
  • Prior leadership experience

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