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

Catalent Pharma Solutions•Madison, WI

4d•Onsite

About The Position

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 our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent. 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.

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.

Nice To Haves

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.

Responsibilities

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.