Senior Quality Control Supervisor
3 weeks ago
The Senior Quality Control Supervisor will lead the QC analytical team, ensuring the highest quality standards are met in the development and manufacturing of new treatments for patients worldwide. This role requires a strong understanding of cGMP practices and the ability to mentor direct reports on scientific and regulatory principles.
Key Responsibilities:
- Supervise the day-to-day operations of the QC department, ensuring staff are fully trained on cGMP manufacturing operations and documentation.
- Drive department process improvements to increase efficiency and compliance.
- Ensure department adherence to batch record, stability protocol timelines, and deliverable dates.
- Responsible for document writing, data interpretation, and statistical analysis.
- Build effective teams and drive engagement to create a culture where employees are motivated to do their best.
Requirements:
- Bachelor's degree in a Life Sciences discipline with 6-8 years of experience in a cGMP QC laboratory.
- Masters' degree in a Life Sciences discipline with 4-6 years of experience in a cGMP QC laboratory.
- Experience with ELISA, ddPCR, qPCR, and Empower 3 preferred but not required.
- Expert knowledge of QC analytical methods used for protein chemistry and molecular biology.
- Experience within the biologic, pharmaceutical, or medical device industry performing direct hands-on work in QC function with a strong familiarity of general GMP practices.
What We Offer:
- Competitive medical benefits and 401K.
- 152 hours PTO + 8 Paid Holidays.
- Dynamic, fast-paced work environment.
- Opportunity to work on Continuous Improvement Processes.
About Catalent:
Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. We are committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.
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