Senior Associate - Quality Assurance Operations, Floor
Listed on 2026-06-06
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Quality Assurance - QA/QC
Quality Engineering, Data Analyst -
Manufacturing / Production
Quality Engineering
Senior Associate I - Quality Assurance Operations Position Summary
Work Schedule:
Mon-Fri 8am-5pm. 100% on-site.
Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer’s.
The Role- Accountable for execution of the QA on the Floor program.
- Performs routine walkthroughs of the Manufacturing Area partnering with manufacturing on Quality best practice implementation and troubleshooting when problems arise.
- Provides direct quality support for routine manufacturing operations.
- Responsible issuance of controlled documents for production, including Batch Production Records, Product Labels and forms.
- Responsible for review of documentation, including batch records, test data, environmental monitoring data, and logbooks, for production of solutions and columns used in the manufacture of bulk drug substance.
- Performs release of produced solutions and columns.
- Assists with inspection of final product containers
- Supports shipment of finished products.
- Responsible for review of facility and equipment records in support of GMP operations.
- Accountable for control and management of Cell Bank inventory
- Notifies Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.
- Perform or support any other tasks necessary to maintain the product quality and site CGMP compliance.
- Files and maintains controlled documents.
- Other duties as assigned.
- Master’s degree in STEM discipline with minimum of 0 years related experience.
- Bachelor's Degree in STEM discipline with minimum of 3 years related experience.
- Associates Degree in STEM discipline with minimum of 6 years related experience.
- High School Diploma with a minimum of 7 years related experience.
- Defined career path and annual performance review and feedback process
- Diverse, inclusive culture
- Positive working environment focusing on continually improving processes to remain innovative
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
- 152 hours of PTO + 8 paid holidays
- Generous 401K match
- Medical, dental and vision benefits effective day one of employment
- Tuition Reimbursement - Let us help you finish your degree or start a new degree!
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to Disabili
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