Associate I, Quality Control

Sentry BioPharma Services, Inc.

Edinburgh, IN0–2 yrs1h agovia LinkedIn

About the Role

Join our dynamic team at Sentry BioPharma Services as a Quality Control Associate, where you will play a vital role in ensuring the quality and safety of pharmaceutical materials. This position offers an excellent opportunity to contribute to a collaborative and innovative laboratory environment dedicated to maintaining the highest standards in pharmaceutical testing and analysis.

Key Responsibilities

  • Receive, label, and safely store samples to be tested, ensuring proper documentation and handling.
  • Perform aliquoting from bulk containers to obtain precise test samples.
  • Organize and store samples in compliance with safety protocols and regulatory requirements to protect personnel and sample integrity.
  • Prepare samples prior to testing, including proper labeling and handling.
  • Set up, calibrate, and troubleshoot laboratory equipment to ensure accurate and reliable testing results.
  • Prepare laboratory equipment and materials for upcoming analyses.
  • Conduct analytical tests on pharmaceutical materials, recording and analyzing results accurately.
  • Record test data meticulously and report findings in accordance with company and regulatory standards.
  • Maintain a clean, organized, and compliant laboratory environment.
  • Support other laboratory functions as needed to ensure smooth operations.

Requirements & Tech Stack

  • Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field.
  • Prior experience in a quality control laboratory, preferably within the pharmaceutical industry.
  • Preferred experience working in an analytical laboratory.
  • Experience with pharmaceutical analyses, and/or analysis of large molecules, a plus.
  • Knowledge of laboratory safety protocols and good laboratory practices (GLP).
  • Proficiency in operating laboratory equipment such as pipettes, balances, and analytical instruments.
  • Ability to follow standard operating procedures (SOPs) and regulatory guidelines.

Qualifications

  • Strong attention to detail and excellent organizational skills.
  • Ability to troubleshoot and resolve equipment issues efficiently.
  • Good documentation and record-keeping skills.
  • Effective communication skills and ability to work collaboratively within a team.

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