Quality Control Supervisor
Location: Denver, CO
Working Situation: Hybrid
Level: Mid-Senior Level
We are working with a dynamic and forward-thinking pharmaceutical company dedicated to improving patient lives through innovation and excellence. With a commitment to quality and integrity, they specialize in developing and manufacturing high-quality pharmaceuticals that address critical medical needs. Our state-of-the-art facilities and cutting-edge technology enable us to deliver products with unparalleled precision and efficacy. We pride ourselves on fostering a collaborative and supportive work environment that drives professional growth and encourages innovation. Join us in our mission to make a meaningful difference in the world of medicine.
The Quality Control Supervisor will oversee a team of analysts engaged in the testing and release of products to ensure manufacturing timelines are met. This role involves supervising the testing of samples, raw materials, and stability samples, as well as leading the team to maintain compliance with FDA and cGMP regulations.
The Quality Control Supervisor will be responsible for:
- Supervise the testing and release processes for products, including cleaning samples, raw materials, and stability samples.
- Provide leadership and training to direct reports, ensuring timely completion of administrative tasks such as time entry, resource allocation, and workload balancing.
- Prioritize and manage projects to meet deadlines, oversee work schedules, and set sample priorities for reporting.
- Ensure all operations, including laboratory functions, comply with FDA and cGMP regulations, and that staff are properly trained.
- Utilize senior analysts for laboratory investigations and advanced technical issues.
- Review and approve technical reports, test methods, and procedural documents; generate Certificates of Analysis and validate analytical results; review stability reports.
- Participate in project teams, meetings, third-party audits, and regulatory audits.
- Monitor departmental expenditures to ensure adherence to the budget.
- Ensure compliance with departmental and regulatory timelines.
- Participate in required hazardous waste training and manage hazardous waste as per procedures.
The Quality Control Supervisor will have the following qualifications:
- Bachelor’s degree in Science, preferably in Chemistry or Biochemistry.
- At least six years of experience in an analytical laboratory environment, including two years in a pharmaceutical GMP setting.
- Previous experience in a supervisory or team lead role is preferred.
If you are interested in this Quality Control Supervisor opportunity, apply now!
