Quality Control Senior Specialist (v343)

  • Contract Duration: 12+ months
  • Manufacturing
  • Boston, MA

Website Lenox Executive Search


Lenox Executive Search is seeking a Quality Control Sr. Specialist, for a 12 month contract position with one of our global pharmaceutical companies, working onsite in Boston, MA.

Key Responsibilities of a Quality Control Sr. Specialist:

  • Analysis of cGMP solid oral dosage samples utilizing various analytical techniques
  • Perform testing independently following established methodology, procedures and SOPs
  • Participate in executing method validations and/or method transfers
  • Troubleshoot analytical methods with the assistance of supervisor when necessary
  • Maintain accurate testing records and adhere to cGMP/GDP expectation
  • May be required to author and review data, SOPs, analytical methods, protocols and reports
  • Participates in compliance related teams working towards the goal of continuous improvement.

Minimum Qualifications of a Quality Control Sr. Specialist:

  • BS/MS and 4+ years of relevant work experience
  • Advanced knowledge of cGMP in a pharmaceutical setting
  • Proficient in basic analytical techniques in a QC/commercial setting (e.g. HPLC, dissolution, GC, KF, etc.), including method validation/transfer
  • Experience with both drug substance and drug product (oral solid dosage forms) testing
  • Must be a committed team player and collaborator

Additional Desired Skills of a Quality Control Sr. Specialist:

  • Experience with electronic notebooks
  • Experience with computerized Quality Management Systems
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– The Lenox Executive Search Team