Quality Control Analyst I – Impactful Biotech QC

Replimune; United Kingdom; Remote; GBP 28,000 - 38,000; Full time

Job summary

Replimune is seeking a QC Technician to perform routine quality control testing in our Milton Park facility. You will follow SOPs, prepare reagents, maintain equipment and support inventory management while ensuring compliant documentation.

Working on-site five days a week, you will review data, assist with audits, and contribute to continuous improvement of QC processes under cGMP and GDP guidelines. A chemistry/biochemistry degree and meticulous attention to detail are essential.

Qualifications

• Degree in Chemistry/Biochemistry or related science.
• Competent analytical skills and attention to detail.
• Understanding of GMP requirements preferred.
• Computer literacy.
• Ability to work independently and with others in a team.

Responsibilities

• Perform QC testing of samples according to SOPs.
• Maintain various cell lines 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 current Good Manufacturing Practices (cGMP) and Good Documentation practices (GDP).
• General lab tasks such as housekeeping, inventory of supplies, order supplies etc.
• Write QC documents and assist with investigations and other documentation as required.
• Assist with internal and regulatory agency audits / inspections.

Skills

Analytical skills

Attention to detail

Computer literacy

Teamwork

Education

BSc Chemistry/Biochemistry or related

Tools

LIMS

MS Office

Job description

Replimune is seeking a QC Technician to perform routine quality control testing in our Milton Park facility. You will follow SOPs, prepare reagents, maintain equipment and support inventory management while ensuring compliant documentation.

Working on-site five days a week, you will review data, assist with audits, and contribute to continuous improvement of QC processes under cGMP and GDP guidelines. A chemistry/biochemistry degree and meticulous attention to detail are essential.