Supervisor, QC - Weekends

at  Thermo Fisher Scientific

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.

INDUSTRY EXPERIENCE

• 5+ years of experience working in a GMP facility and/or regulated environment and in a Quality Control Role.
• 3+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)

KNOWLEDGE, SKILLS, ABILITIES

• 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.

DISCLAIMER:

This job description presents the general content and requirements for the performance of this job. The description is not to be construed as an extensive statement of work, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.
Nothing contained herein should be construed to describe an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully abide by all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
Thermo Fisher Scientific is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We strive to build an inclusionary work environment and prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

• 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.