Radiopharmaceutical Manufacturing Specialist (3rd shift)

Execute various aspects of radiopharmaceutical manufacturing

• Pre-production set-up
• Manufacturing processes
• Post-production activities
• Waste stream management

Assist in record preparation and completion

• Batch Records
• Forms
• Logbooks

Review and document production

• Production Work Orders
• cGMP documentations (BPR, SOP, WI, Production Checklists)

Perform safety checks and inspections

• Production processing equipment
• Control systems
• Consumables
• Cleanrooms

Maintain inventory and equipment traceability

• Materials
• Consumables
• Under direction of the leader

Contribute to cross-functional projects

• Production scale-up
• Continuous process improvement

Qualifications

• Associate’s Degree (AS) in a STEM discipline and minimum two (2) years of cGMP experience
• Equivalent combination of education and experience
• Bachelor’s Degree (BS) in a STEM discipline and minimum two (2) years of cGMP experience preferred
• CDMO/CMO experience
• Chemistry experience and knowledge of aseptic processes (cleanroom environment) and equipment qualification preferred