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 Information
 
This position supports the Quality Control Analytical team for our Biologics Division in St. Louis, MO
 
 
How will you make an impact?
 
In this key role you will supervise the QC- analytical laboratory to assure the chemical quality of products and materials in our St. Louis facility.
 
 
What will you do?
 
 

• 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 organizational 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.
• Overall creation and coordination of work schedules for team.
• Revise/review specifications, SOPs, and other documents regarding QC-Analytical as well as HPLC testing and assay execution.
• Oversee HPLC testing program as subject matter expert.
• Train new hires on department processes, procedures and tools.
• Lead investigations in the case of deviations.
• Interact with auditors/clients during visits and tours.
• Oversee daily activities for the HPLC group to ensure appropriate quality output and maintenance of schedules.
• Review and approval of documentation generated by the group.
• Effectively communicate with peers, manufacturing, AD and QC staff, to resolve technical issues and direct activities.

• Minimum of 3 years’ experience in quality/analytical/pharmaceutical industry or similar experience.
• At least 2 years supervisory/ team lead experience within the pharmaceutical industry.
• At least 5 years of HPLC (High-performance liquid chromatography) experience in industry.
• Experience with advanced LC assays such as: Peptide map, Glycan analysis, Reverse Phase, SEC, Titer, CEX is a plus.
• Knowledge of QC chemistry techniques, with some experience with FDA Drug GMP regulations in cGMP manufacturing environment.

• Ability to drive functional, technical and operational excellence.
• Ability to inspire and foster innovation, collaboration, transparency and team effectiveness.
• Working knowledge of Empower is a plus.

 
 
 
 
This position has not been approved to provide relocation assistance
 
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com. 
 
 
 
 
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.