Scientist, QC

We're hiring a Scientist, QC to support the stability team in Bloomington, Indiana!

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. 

Catalent Biologics in Bloomington, Indiana is a state-of-the art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.

The Scientist, QC is a part of the stability team which is responsible for analytical testing, data analysis, document writing, and data reporting to support of ICH stability studies to determine the stability of bulk drug substance and drug product. This is a full-time, salaried position and is 100% site based. The schedule is Monday – Friday, 1st shift.

The Role

• Independently executes and properly documents cGMP Quality Control testing.

• Independently operates basic and moderately complex cGMP Quality Control equipment.

• Assists in authoring technical documents such as SOPs and reports.

• Enters data into Laboratory Information Management System (LIMS) or laboratory reports.

• Performs general lab housekeeping in adherence to 5S standards.

• Initiates and assists with records in TrackWise.

• Other duties as assigned.

The Candidate

• Bachelor’s degree in science field with a minimum of 3 years of experience, including 1-year GMP experience or regulated industry; Master’s degree in science field, with 1-year GMP experience or regulated industry; PhD in science field, with GMP experience preferred.

• General laboratory equipment experience, including micropipettes.

• Prior experience in cGMP QC testing, highly preferred.

• Prior experience in cGMP stability testing, highly preferred.

• Experience using LIMS and Trackwise, highly preferred.

• Must be able to read and understand English-written job instructions and safety requirements.

Why you should join Catalent

• Medical, dental, vision, and wellness benefits are effective on the first day of employment.

• Potential for career growth on an expanding team and organization.

• 152 hours of paid time off annually plus 8 paid holidays.

• Community engagement and green initiatives.

• Engaging D&I Employee Resource Groups.

• Tuition reimbursement program.

• Generous 401K match.

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