Scientist - Quality Control, AQC

Scientist I, Quality Control

Position Summary:

Work Schedule:

M-F 8am-5pm, 100% on-site. The Quality Control (QC) team is responsible for testing products, raw materials, and the manufacturing environment to ensure the Safety, Quality, Identity, Purity, and Potency produced by the Catalent Madison Biologics facility. The position requires routine testing of process samples, raw materials, finished products, and stability samples while adhering to SOPs and working in a cGMP compliant environment.

The role includes analyzing and interpreting results, supporting preventive maintenance, data review/archiving, database entry/review, and contributing to process improvement initiatives.

• Independently executes and properly documents cGMP Quality Control testing.
• Independently operates basic and moderately complex cGMP Quality Control equipment.
• Assists in authoring technical documents such as SOPs and reports.
• Performs self-review of analytical data for accuracy and consistency with SOP.
• Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
• Performs general lab housekeeping in adherence to 5S standards.
• Initiates and assists with records in Trackwise.
• Accurately completes routine and preventive maintenance on basic to moderately complex equipment.
• Actively participates in team meetings and/or training sessions.
• Other duties as assigned.

• Master’s Degree in Biology, Biotechnology, Chemistry or related life sciences field.
• Bachelor’s Degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 3 years of industry experience.
• Associate Degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 6 years of industry experience.
• High School Diploma or equivalent with a minimum of 7 years of industry experience.
• Strong understanding of analytical chemistry and simple and moderately complex lab equipment.
• Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
• cGMP, Good Documentation Practices (GDP) or Good Laboratory Practices (GLP) knowledge.
• General laboratory equipment experience, including micropipettes.

• Defined career path and annual performance review and feedback process.
• Diverse, inclusive culture.
• Positive working environment focusing on continually improving processes.
• Potential for career growth on an expanding team.
• 152 hours of PTO + 8 paid holidays.
• Generous 401(k) match.
• Medical, dental and vision benefits effective day one of employment.
• Tuition Reimbursement.

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 email to Disabili