Analytical Development Scientist I, GMP & Methods

Replimune-2; Abingdon; On-site; GBP 42,000 - 65,000; Full time

Benefits offered by this job

Equal Opportunity Employer

Job summary

Replimune is seeking an Analytical Development Scientist I to join the Milton Park site on a five‑day on‑site basis. You will perform routine in‑house analytical testing (PCR, ELISA, chromatography, cell‑based assays) to support AD, PD, R&D and QC projects and contribute to method development and validation under GMP guidance.

With 4–5+ years in a cGMP environment, you will prepare reagents, maintain equipment, and help troubleshoot data while collaborating with cross‑functional teams.

Qualifications

• Bachelor’s degree in a biological science is required; MSc or PhD preferred.
• 4-5+ years industry experience, preferably in a cGMP Quality environment.
• Good time management and the ability to work both independently and in a small team.

Responsibilities

• Perform in-house in-process and stability testing (PCR, ELISA, chromatography and cell-based tests) to support PD, AD, R&D and QC testing.
• Provide support by performing analytical method development and product characterization projects.
• Prepare laboratory reagents and controls for routine testing and development projects.
• Support development of robust analytical test methods in line with regulatory requirements.
• Execute qualification and validation of analytical methods and technology transfer per ICH and other guidelines.
• Oversee equipment maintenance, calibration and verification and handle GMP documentation.

Skills

Time management

Independent worker

Communication

Analytical thinking

Statistical analysis

Education

Bachelor’s degree in biological science

MSc or PhD preferred

Tools

Microsoft Word

Excel

Outlook

Statistical analysis software

Job description

Replimune is seeking an Analytical Development Scientist I to join the Milton Park site on a five‑day on‑site basis. You will perform routine in‑house analytical testing (PCR, ELISA, chromatography, cell‑based assays) to support AD, PD, R&D and QC projects and contribute to method development and validation under GMP guidance.

With 4–5+ years in a cGMP environment, you will prepare reagents, maintain equipment, and help troubleshoot data while collaborating with cross‑functional teams.