Role: QC Specialist
Location: Boston, MA / Chicago, IL / San Jose, CA - Multiple sites
Duration: Long Term
**No C2C**
Job Summary: We are seeking a detail-oriented and experienced Quality Control (QC) Specialist to ensure the integrity and compliance of pharmaceutical products with regulatory standards. The QC Specialist will be responsible for testing raw materials, in-process samples, and finished products to ensure they meet established specifications and quality standards. This role will also support investigations, ensure accurate documentation, and maintain compliance with Good Manufacturing Practices (GMP) and industry regulations.
Key Responsibilities:
- Perform routine testing on raw materials, in-process samples, and finished products according to approved methods and SOPs.
- Conduct stability testing and ensure results meet required specifications.
- Document all analytical work accurately and ensure compliance with GMP and regulatory requirements.
- Support quality investigations, root cause analysis, and deviations to identify areas for improvement.
- Ensure proper calibration and maintenance of laboratory equipment.
- Review and approve test results, ensuring accurate and timely reporting.
- Participate in internal and external audits, ensuring inspection readiness.
- Collaborate with cross-functional teams to address quality concerns and ensure smooth workflow.
Qualifications:
- Bachelor’s degree in Chemistry, Biology, or related field.
- Minimum of 2-3 years of experience in a QC role within the pharmaceutical industry.
- Strong knowledge of GMP, GLP, and regulatory requirements.
- Hands-on experience with analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy.
If you are looking for any other roles in the Life Sciences Industry, feel free to share your resume to sai@premierlifesciences.com along with the role of your interest - we are happy to provide H1B sponsorship & H1T if required.
**No C2C enquiries please**