Supervisor, QC Analytical (Fri-Mon)

Thermo Fisher Scientific•St. Louis, MO

19h•Onsite

About The Position

This position supports the QC Analytical team for our Biologics Division in St. Louis, MO. The QC Analytical Supervisor will be responsible for managing the weekend (Fri-Mon) team of laboratory analyst and data reviewers. This position offers the chance to lead a newer developed team within a rapidly growing site, surrounded by collaborative colleagues and supported by an exceptional organizational strategy.

Requirements

Bachelor’s Degree in a Biological Science related field.
At least five years of experience working in a GMP facility and/or regulated environment and in a Quality Control Role.
At least three years’ experience working in a role performing 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 is essential.
Ability to understand customer requirements related to Quality control, including processes and equipment.
Ability to perform structured problem-solving techniques in an analytical laboratory.
Outstanding technical writing skills.
Strong interpersonal skills including actively listening, conflict resolution and the ability to effectively influence diverse stakeholders for positive outcome.
Highly organized with attention to detail.
Ability to drive functional, technical and operational excellence.
Ability to inspire and foster innovation, collaboration, transparency and team effectiveness.
Must be able to cover Friday-Monday, 10 hr shifts.
Ability to lift up to 25 lbs independently, with occasional heavier objects of up to 50lbs with assistance.
Must be able to wear gloves and other PPE to handle samples.
Must be able to stand for extended periods of time, as needed.

Responsibilities

Manage Weekends (Fri-Mon) 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 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.
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.