QC Chemistry Lead: Validate, Transfer & Improve Methods

225 Cardinal Health 414, LLC; Indianapolis (IN); On-site; USD 82,000 - 117,000; Full time

Benefits offered by this job

Medical/Dental/Vision

PTO

401k

MyFlexPay

FSAs

Disability

Work-Life resources

Parental leave

Wellness programs

Job summary

Cardinal Health, Inc. is seeking a Supervisor, Quality Control (Chemistry) to lead the QC Chemistry team at our Indianapolis facility.

You will supervise chemists and support staff, oversee method validation/verification, and ensure compliance with regulatory requirements. The role requires a Bachelor’s degree in chemistry or related field, 5+ years in FDA-regulated environments, and strong technical writing with experience in validation and technology transfer.

Qualifications

• Bachelor’s degree in chemistry or related science field.
• Experience in radiochemistry, nuclear pharmacy, or health physics preferred.
• 5+ years of relevant work experience with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device).
• Experience with equipment qualification, software validation, test method validation, and/or process validation.
• Strong technical writing skills; proficient with Microsoft Word and Excel.

Responsibilities

• Coordinate and supervise daily activities of chemists or staff in technology transfer, method validation/verification and optimization.
• Liaise between Cardinal Health QC and Client QC for technology transfer and validation/development.
• Lead QC Chemistry team and identify quality events for QA/QC management review.
• Oversee analysts and contractors operating analytical equipment and documenting results per SOPs.

Education

Bachelor’s degree in chemistry or related science field

Tools

Microsoft Word

Microsoft Excel

Job description

Cardinal Health, Inc. is seeking a Supervisor, Quality Control (Chemistry) to lead the QC Chemistry team at our Indianapolis facility.

You will supervise chemists and support staff, oversee method validation/verification, and ensure compliance with regulatory requirements. The role requires a Bachelor’s degree in chemistry or related field, 5+ years in FDA-regulated environments, and strong technical writing with experience in validation and technology transfer.