GMP Radiopharmaceutical Process Scientist

Cardinal Health, Inc.; New Augusta (IN); On-site; USD 92,000 - 118,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off plan

Health savings account (HSA)

401k savings plan

Access to wages before pay day with my

Flexible spending accounts (FSAs)

Disability coverage

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Job summary

Cardinal Health, Inc. in Indianapolis manages nuclear manufacturing for time-sensitive radiopharmaceuticals in a highly regulated setting. You will produce clinical trial materials, support technology transfer, and ensure adherence to GMP, safety and quality standards.

The role emphasizes data integrity, documentation, and collaboration across teams, with potential off-shift hours to align with production schedules. Anticipated salary range is disclosed and benefits are extensive.

Qualifications

• 4-8 years of experience, preferred
• Bachelor's degree in life sciences or engineering with at least four years of experience in a GMP manufacturing environment
• Background in product research and development preferred
• Experience in working in a clean room environment with EH&S regulation

Responsibilities

• Perform and execute production for client drug products, including routine clinical trial manufacturing and developmental studies.
• Evaluate and transfer testing procedures for radiopharmaceutical manufacturing facilities.
• Assist on creation of protocols and documentation for technology transfer and qualification.
• Lead investigations and document deviations during technology transfer and routine production.
• Train facility personnel on new procedures and support after transfer.
• Facilitate operation, maintenance and repair of manufacturing equipment.
• Communicate safety, quality and compliance issues to leadership.
• Create and modify SOPs and relevant maintenance documentation.
• Provide input to product development regarding sponsor product manufacturing.

Skills

GMP manufacturing experience

Data integrity

Documentation practices

Team collaboration

Safety compliance

Education

Bachelor's degree in life sciences or engineering

Bachelor’s degree in related field or equivalent

Job description

Cardinal Health, Inc. in Indianapolis manages nuclear manufacturing for time-sensitive radiopharmaceuticals in a highly regulated setting. You will produce clinical trial materials, support technology transfer, and ensure adherence to GMP, safety and quality standards.

The role emphasizes data integrity, documentation, and collaboration across teams, with potential off-shift hours to align with production schedules. Anticipated salary range is disclosed and benefits are extensive.