Associate Scientist - Quality Control, AQC

Associate Scientist I
- Quality Control, AQC Position Summary

Work Schedule:

M-F 8am-5pm

100% on-site

Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist I
- Quality Control, Raw Materials. This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained in technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.

• 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 lift and/or move up to 10 pounds and occasional lifting and/or moving 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.

• 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:
  Basic understanding of analytical chemistry and simple lab equipment.
• Preferred:
  Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
• Preferred: cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge.
• Preferred:
  Experience following standard operating procedures (SOP).
• Preferred:
  General laboratory equipment experience, including micropipettes.

• 152 hours of PTO + 8 paid holidays.

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, confirming your request for an accommodation and including the job number, title and location to Disabili This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.