PET Radiochemistry QC Chemist - Method Dev & GMP QC

Perceptive; Greater London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A pharmaceutical company is seeking a full-time QC professional to perform method development and analysis of PET radiotracers in a GMP environment. The role involves routine QC support for clinical studies and ensuring compliance with regulations. Candidates should have a degree in Chemistry, at least 2 years of experience in a QC laboratory, and expertise in HPLC. This position is vital for supporting both clinical and pre-clinical studies, making it essential for maintaining high standards in the lab.

Benefits

25 days holiday

Private Healthcare

Company Pension Scheme

Annual staff bonus scheme

Cycle to Work scheme

Qualifications

• Minimum 2 years experience in a QC laboratory.
• Experience in HPLC.
• Experience in aGMP environment.

Responsibilities

• Perform QC of assigned radiotracers according to project distribution.
• Implement QC for newly assigned radiotracers: development, validation, documentation.
• Provide routine QC support for clinical and pre‑clinical studies.
• Support analytical chemistry for radiotracer characterization.
• Data processing including HPLC and GC.
• Document QC records for compliance with cGMP.
• Raise and investigate Out Of Specification (OOS) results within QMS.
• Present technical QC issues for internal and external audits.
• Train and educate others in your area of expertise.
• Maintain relevant procedures and keep up-to-date with new techniques.
• Present results to internal and external audiences.
• Ensure adequate stocks of laboratory supplies.
• Complete routine laboratory tasks such as preparing HPLC buffers.

Skills

HPLC experience

Minimum 2 years experience in a QC laboratory

Experience in aGMP environment

Education

Undergraduate degree in Chemistry or a related scientific discipline

Job description

A pharmaceutical company is seeking a full-time QC professional to perform method development and analysis of PET radiotracers in a GMP environment. The role involves routine QC support for clinical studies and ensuring compliance with regulations. Candidates should have a degree in Chemistry, at least 2 years of experience in a QC laboratory, and expertise in HPLC. This position is vital for supporting both clinical and pre-clinical studies, making it essential for maintaining high standards in the lab.