Work Schedule
10 hr shift/nights
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Supervisor, Quality Control
When you're part of the team at Thermo Fisher Scientific (TFS), 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
We have industry leading sterile injectable facilities providing solutions to take product from Pre-Clinical to the market. Pharmaceutical products come in many different dose forms including inhalations, oral dose, and injectables.
Hours
This is a third shift role, 10 hour shifts Tues-Fri 6pm-4am (this includes on call support on rotating basis over weekend).
How to make an impact on the TFS team
Provide technical leadership and Quality oversight in association with specific aspects of Environmental Monitoring (EM) to ensure compliance with regulations that govern pharmaceuticals. Establish actions and implement systems to achieve process improvements and efficiencies to address shortcomings. As Supervisor, offer assistance in problem-solving, failure analysis, and quality or process system design activities. Implement approved changes to policies and procedures in collaboration with labs, production, regulatory, quality, and clients. Engage your team in keeping safety in forefront. Thermo Fisher is an equal opportunity employer.
How to contribute to the team
Independently review and audit EM documentation and investigation report discrepancies and coordinate corrections/revisions. Coordinate your staff on day-to-day operations of multiple quality operations and assist with audits and regulatory inspections.
Conduct risk assessments with a cross-functional team and take appropriate actions to ensure adequate controls in relation to the level of product quality, safety, and business risks.
Provide oversight in the review/approval of EM records and data, as well as helping to meet goals for batch dispositions, assessment, investigations and validation projects. Evaluate protocols, procedures, and results for scientific and/or business merit.
How will you get here?
Education/Experience
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