What are the responsibilities and job description for the Associate I, Quality Control position at Sentry BioPharma Services, Inc.?
Description
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
Requirements
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.
- Prior experience in a quality control laboratory, preferably within the pharmaceutical industry.
- Knowledge of laboratory safety protocols and good laboratory practices (GLP).
- Proficiency in operating laboratory equipment such as pipettes, balances, and analytical instruments.
- 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.
- Ability to follow standard operating procedures (SOPs) and regulatory guidelines.
Requirements
- Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field.
- Preferred experience working in an analytical laboratory. Experience with pharmaceutical analyses, and/or analysis of large molecules, a plus.