GMP QC Specialist – Radiopharmaceuticals

Telix Pharmaceuticals Limited; Angleton (TX); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive salaries

Performance-based bonuses

Learning and development support

Generous vacation and wellness days

Job summary

Telix Pharmaceuticals Limited is seeking a QC Specialist to support GMP operations at their Angleton site. The ideal candidate will have a Bachelor’s degree and at least 3 years in a GMP lab. Responsibilities include executing QC testing, ensuring compliance with GMP, and managing quality investigations. The position emphasizes collaboration and a commitment to safety in handling radioactive materials. Competitive salary, bonuses, and professional development opportunities are offered within a supportive environment.

Qualifications

• Minimum of 3 years of experience in a laboratory role within a GMP environment.
• Experience in GxP manufacturing operations is preferred.
• Willingness to work with radioactive materials.

Responsibilities

• Execute lab operations to ensure compliance with GMP principles.
• Review QC testing data for accuracy to support batch release.
• Participate in writing and updating Quality Control procedures.

Skills

Analytical testing

GMP compliance

Collaboration

Aseptic technique

Problem-solving

Education

Bachelor’s degree in chemistry, biochemistry, biology, or related field

Tools

HPLC

GC

TLC

Elisa

CE-SDS

Job description

Telix Pharmaceuticals Limited is seeking a QC Specialist to support GMP operations at their Angleton site. The ideal candidate will have a Bachelor’s degree and at least 3 years in a GMP lab. Responsibilities include executing QC testing, ensuring compliance with GMP, and managing quality investigations. The position emphasizes collaboration and a commitment to safety in handling radioactive materials. Competitive salary, bonuses, and professional development opportunities are offered within a supportive environment.