Quality Control Analyst Jobs

Specific Responsibilities:

• Perform daily cGMP quality control laboratory microbiological testing activities at the iCTC facility.

• Perform environmental monitoring of the cleanroom areas as scheduled.

• Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times.

• Perform all activities with respect to cGMP compliance.

• Support thorough cGMP investigations for out-of-specification test results.

• Support technical problem-solving.

• Support product stability programs, including execution of stability testing, stability data analysis, and final reporting of stability data.

• Operate at a consistent and exemplary efficiency level, producing high-quality and accurate results.

Education and Qualifications:

• Bachelor’s degree in a relevant discipline (biological sciences or equivalent).

• Minimum one (1) year of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus.

• Successfully interface with multi-disciplined teams.

• Extremely detail-oriented with strong technical skills.

• Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity.

• High level of ownership and accountability.

• Demonstrate a sense of urgency; ability to recognize time sensitivity.

Hours/Shifts: Monday to Friday, 4:30 pm - 1:30 am EST