QC Analyst II

Abingdon-On-Thames, England, United Kingdom

6/24/2025

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease.

 At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold and Innovative.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other .

People are at the center of everything we do, and when it comes to our employees , we make it personal .   With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to  contribute to the meaningful work we do which could impact the lives of patients .

Join us, as we reshape the future.

Job Summary:

This role will be responsible for performing the routine QC testing following Standard Operating Procedures (SOPs) and established test methods. They will also perform various laboratory-based activities such as reagent preparation, tissue culture, equipment maintenance, sample receipt and disposal etc. The role involves getting involved in other tasks such as maintaining sample/reagent/consumable inventory and ordering reagents, updating forms and SOPs and writing as well are reviewing QC documents.

This position is based in our Milton Park location and typically has a 5-day on-site expectation.

Responsibilities

The responsibilities of the QC Analyst II include, but are not limited, to the following:

• Perform QC testing of various samples according to Standard Operating Procedures (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 and troubleshooting 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 deviations and CAPAs/ Change controls and assist with investigations and other documentation as required.
• Assist with internal and regulatory agency audits / inspections.
  
  

Qualifications

Education:  

• Degree in Chemistry/Biochemistry/ other related science  
  
  

Required Experience:

• 1-3 years of experience working in GMP/GLP environment or similar set up
• Competent analytical skills and attention for details.
• Understanding of GMP requirements preferred
• Computer literacy
• Ability to work independently and with others in a team