Associate Scientist I - Quality Control, AQC (2nd shift)

Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients. The business includes proprietary GPEx cell line engineering, a state-of-the-art biomanufacturing facility in Madison, WI, and leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA.

About the role

• Executes and properly documents cGMP Quality Control testing with supervision.
• Operates basic cGMP Quality Control equipment.
• Performs self-review of analytical data for accuracy and consistency with SOP.
• Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
• Frequently lifts and/or moves up to 10 pounds and occasionally lifts and/or moves up to 50 pounds.
• Handles products using material handling equipment.
• Conducts inspections on inbound single-use manufacturing materials in a warehouse environment.
• Performs general lab housekeeping in adherence to 5S standards.
• Accurately completes routine and preventive maintenance on basic equipment.
• Actively participates in team meetings and/or training sessions.
• Other duties as assigned.

Requirements

• Bachelor’s Degree in Biology, Biotechnology, Chemistry, or related life sciences field.
• Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 1 year of industry experience.
• High School Diploma or equivalent with a minimum of 4 years of industry experience.

Preferred Qualifications

• Basic understanding of analytical chemistry and simple 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.
• Experience following standard operating procedures (SOP).
• General laboratory equipment experience, including micropipettes.

Benefits

• 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.

Schedule

Monday–Friday, 11:00 AM–7:00 PM (2nd shift), 100% on-site.