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

Catalent Pharma Solutions; Madison (WI); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

152 hours of PTO

8 paid holidays

Career growth opportunities

Job summary

Catalent Biologics in Madison, WI seeks an Associate Scientist I - Quality Control to execute and document cGMP QC testing on 2nd shift, 11am-7pm, on-site. The role supports our biomanufacturing and analytical services teams, with responsibilities including equipment operation, data entry into LIMS, and ensuring accuracy of results.

The ideal candidate holds a Bachelor's in biology/chemistry or an associated degree with industry experience; strong documentation, SOP adherence, and familiarity

Qualifications

• 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, GDP, or GLP knowledge.
• Preferred: Experience following SOPs.
• Preferred: 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.

Education

Bachelor’s Degree in Biology, Biotechnology, Chemistry, or related life sciences field

Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field

High School Diploma or equivalent

Tools

LIMS

Job description

Associate Scientist I - Quality Control, AQC

Work Schedule: M-F 11am-7pm (2nd shift) 100% on-site

Position Summary

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.

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 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.

The Candidate

• 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.

Why you should join Catalent

• 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
• Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities.

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, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. 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.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time-tested experience in development sciences, delivery technologies, and multi‑modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.