Quality Control Lab Analyst I (On-Site GMP)

Replimune; Abingdon; On-site; GBP 26,000 - 38,000; Full time

Job summary

Replimune is seeking a QC technician to perform routine quality control testing in accordance with SOPs and established methods. You will handle reagent preparation, tissue culture, equipment maintenance, and sample receipt while maintaining accurate inventory and documentation.

This on-site role at Milton Park typically requires five days per week on site, with involvement in SOP updates and internal/regulatory audits to ensure GMP compliance.

Qualifications

• Competent analytical skills and attention for detail.
• Understanding of GMP requirements preferred.
• Computer literacy.
• Ability to work independently and with others in a team.

Responsibilities

• Perform QC testing of various samples according to SOPs.
• Maintain various cell lines on regular basis by revival and passaging at set intervals.
• Review testing data and records of other operators and data verification for reports.
• Perform QC sample and material receipt and maintain inventory.
• Routine equipment maintenance as required.
• Write or revise SOPs, protocols, forms and update as required.
• Participate in QC method transfers, qualification, and stability activities.
• Adhere to cGMP and GDP practices.
• General lab tasks such as housekeeping and inventory management.
• Write QC documents and assist with investigations and other documentation as required.
• Assist with internal and regulatory agency audits / inspections.

Skills

Analytical skills

GMP awareness

Computer literacy

Teamwork

Education

Degree in Chemistry/Biochemistry/ related science

Job description

Replimune is seeking a QC technician to perform routine quality control testing in accordance with SOPs and established methods. You will handle reagent preparation, tissue culture, equipment maintenance, and sample receipt while maintaining accurate inventory and documentation.

This on-site role at Milton Park typically requires five days per week on site, with involvement in SOP updates and internal/regulatory audits to ensure GMP compliance.