Lead PET Lab Supervisor - Nuclear Medicine

Pharmalogic Holdings; Austin (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

PharmaLogic is hiring a PET Laboratory Supervisor in Austin, TX to oversee day-to-day operations of the laboratory, ensuring safe, compliant production of radiopharmaceuticals and leading a team of technicians and chemists.

You will partner with the PET Facility Manager to maintain cGMP compliance, manage production schedules and budgets, and drive continuous improvement in quality and safety within a fast-paced radiopharmaceutical environment.

Qualifications

• Bachelor’s degree in chemistry or related technical field preferred.
• Two years of PET manufacturing experience or equivalent preferred.
• Strong communication skills are required.
• Familiarity with GMP manufacturing environment and FDA cGMP regulations required.
• Experience with radiochemistry techniques and analytical equipment troubleshooting highly preferred.

Responsibilities

• Supervise and assist in the preparation of PET isotopes and radiopharmaceuticals, including packaging and shipping of radioisotopes.
• Support manager in meeting all financial goals and objectives by ensuring the facility operates within budget and manages costs.
• Assist PET Facility Manager in managing a team of PET Production Technicians and PET Chemists.
• Facilitate a strong communication channel between site QA and production personnel.
• Follow SOP guidelines for QC release testing of radiopharmaceutical products and ensure regulatory compliance.

Skills

Strong communication skills

Multi-tasking

Team collaboration

Adaptability

Education

Bachelor’s degree in chemistry or related field

Tools

HPLC

GC

TLC

Radiochemistry equipment

Job description

PharmaLogic is hiring a PET Laboratory Supervisor in Austin, TX to oversee day-to-day operations of the laboratory, ensuring safe, compliant production of radiopharmaceuticals and leading a team of technicians and chemists.

You will partner with the PET Facility Manager to maintain cGMP compliance, manage production schedules and budgets, and drive continuous improvement in quality and safety within a fast-paced radiopharmaceutical environment.