Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals.

Location/Division Specific Information

This position supports the quality control team for our Biologics Division in St. Louis, MO.

How will you make an impact?

The QC Analytical Supervisor will lead a sub-set of the Bioassay team of laboratory analysts and data reviewers. This position offers the chance to lead at rapidly growing site, surrounded by collaborative colleagues and supported by an exceptional organizational strategy.

• Handle scheduling for both analytical testing and data review.
• Author, review, and approve laboratory raw data, Laboratory Incidents (Invalid Assays), Deviations, OOS and OOT investigations.
• Support the engineering and validation teams' tasks to assist with equipment commissioning and decommissioning actions, including change controls.
• Perform or schedule laboratory walkthroughs focused on compliance, safety, and efficiency.
• Provide leadership to assigned staff by performing the following: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed, meeting their personal career goals while also achieving departmental goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement and creating a climate where staff are motivated to do their best.

• Author and/or revise internal procedures, test methods, specifications, and other QC documents.
• Review and approve Certificate of Testing, validation reports, and other analytical reports.
• Provide support to site Safety initiatives.
• Other job duties as assigned.

• Bachelor's Degree in a Biological Science related field.

• 5+ years of working in a GMP facility and in a Quality Control Role preferred
• Previous performance of analytical testing on pharmaceutical product(s).
• At least one year experience with analytical method lifecycle (development, qualification, transfer, and/or validation)

• Routine use of MS Excel, MS PowerPoint, MS Teams, and MS Word
• Understanding of requirements related to Quality control, including processes and equipment.
• A passion for excellent customer experiences and process improvements
• Strong problem solving avility in analytical laboratory.
• Outstanding technical writing skills.
• Strong communication including actively listening, conflict resolution and the ability to effectively influence diverse collaborators for positive outcome.
• Highly organized with attention to detail.

• An inspiring demeanor that will encourage innovation, collaboration, clarity and team effectiveness.