Responsibilities of the Senior QC Analyst:

• Oversee sampling and storage of QC samples and maintain inventory.
• Perform routine/non-routine testing of in-process, final product, raw material samples in accordance with Standard Operating Procedures
• Responsible for protocol and report generation, as required.
• Perform sample management such as receipt, inventory, tracking
• Trend data and aid in compilation of trend reports.
• Complete documentation in accordance with current Good Manufacturing Practices (cGMP).
• Maintenance of laboratory equipment/instruments and systems to ensure compliance.

Requirements of the Senior QC Analyst:

• Bachelor’s degree in biology, chemistry or other life science and at least 1-5 years of relevant industry experience in Quality Control in a Pharmaceutical/Biotech GMP environment.
• Proven ability to work independently as well as to collaborate and communicate effectively and work effectively in a team-oriented environment.
• Working knowledge of current Good Laboratory Practices.