Associate Scientist I - Quality Control

Catalent • Madison, WI

6h • Onsite

About The Position

Associate Scientist I - Quality Control
Position Summary:
Work Schedule: Monday – Friday, core hours 8am-4pm
100% on-site (Madison, WI)
Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO). Located in Madison, WI, this facility features advanced mammalian cell line engineering and biomanufacturing capabilities using single-use systems to support scalable production. This 263,000 sq. ft. Good Manufacturing Practice (GMP) facility offers integrated formulation and analytical services to address complex development challenges in Biologics.
The Associate Scientist I in the Quality Control (QC) environmental monitoring team will be responsible for testing products, raw materials and the manufacturing environment to ensure Safety, Quality, Identity, Purity and Potency produced by the Catalent Madison Biologics facility. You will support evaluation of the effectiveness of microbial controls necessary to ensure that the manufacturing facility is maintained in a manner that prevents the ingress of microorganisms in low bioburden products by performing routine and investigational sampling of the manufacturing environment and associated facilities.

Requirements

• High School Diploma or equivalent with four (4) years of industry experience is required. We will also accept the following experience and education (Biology, Biotech, Chemistry, or related field) combinations: Associate’s Degree and one (1) year of experience, or a Bachelor’s without formal experience
• Must have ability to maintain batch records and/or laboratory notebook and complete all laboratory documentation in clear and accurate language and according to SOP
• Must be able to attend training and apply learning on routine operation, maintenance and theory or laboratory instrumentation, SOPs, and regulatory guidelines
• Ability to peer review data to ensure data is well organized with complete documentation. Must have strong use of Excel, Word, and other office systems. Ability to add, subtract, multiply, divide and to record, balance, and check results for accuracy
• Must be able to apply GMPs to everyday work with regard to documentation and instrument use
• Ability to apply regulatory authority and guidelines with training
• Physical requirements: Individual must be able to see, hear, read, and write clear English. Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities

Nice To Haves

• Preferred experience with writing technical documents, maintaining and troubleshooting Quality Control equipment, and familiarity with clean room procedure, aseptic technique, and general lab equipment experience

Responsibilities

• Performs solution preparations and facility monitoring of gas and water sampling. Log in samples into laboratory tracking software
• Perform routine Environmental Monitoring (EM) in manufacturing environment: active air sampling, non-viable particulate monitoring, surface and personnel sampling
• Performs general lab housekeeping in adherence to 5S standards
• Stages materials/components for use within cGMP Quality Control lab
• Accurately completes routine and preventive maintenance on basic equipment
• Actively participates in team meetings and/or training sessions
• Additional functions within the Quality Control department include technical data review, training, instrument maintenance, lead investigations, and laboratory information management system (LIMS) administration. These functions directly support the entire Quality Control department while performing their specific job functions
• Other duties as assigned

Benefits

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• 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
• Tuition Reimbursement - Let us help you finish your degree or start a new degree!

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED