Associate Scientist I - Quality Control

Catalent Pharma Solutions • Madison, WI

1d • Onsite

About The Position

Associate Scientist I - Quality Control Position Summary: Work Schedule: Sun- Wednesday 8am-6pm 100% on-site 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. The Associate Scientist I requires a variety of skills necessary for biotech company operations. The Associate Scientist I is an entry level laboratory role with the expectation that the candidate is able to be trained on 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

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.
• Performs solution preparations.
• Performs environmental monitoring 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.
• Other duties as assigned.

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
• Generous 401K match
• Medical, dental and vision benefits effective day one of employment
• 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
• Number of Employees: 5,001-10,000 employees