Quality Control Analyst - Chemistry & Stability (GMP)

Moderna; Oxford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A biotechnology firm in Oxford is seeking a skilled Quality Control professional to support GMP-compliant stability and analytical testing. You'll manage cGMP documentation, perform various analytical techniques, and contribute to global health initiatives. The ideal candidate has a degree in Chemistry or Biology and substantial experience in a pharmaceutical quality control environment. This role offers a chance to work in a pioneering organization focusing on innovative medical solutions.

Benefits

Quality healthcare and insurance benefits

Generous paid time off

Free access to fitness and mindfulness classes

Qualifications

• 5-7 years in Quality Control Laboratory of a Pharmaceutical Company.
• Strong understanding of GxP regulations (GMP, GLP, etc.).
• Must be on-site full-time; not eligible for remote work.

Responsibilities

• Execute analytical chemistry and stability testing.
• Support cGMP documentation for analytical work.
• Conduct stability program operations and data management.

Skills

Analytical techniques

cGMP compliance

Data analysis

Laboratory operations

Education

BA/BSc in Chemistry or Biology

Tools

HPLC

LIMS (LabVantage)

Job description

A biotechnology firm in Oxford is seeking a skilled Quality Control professional to support GMP-compliant stability and analytical testing. You'll manage cGMP documentation, perform various analytical techniques, and contribute to global health initiatives. The ideal candidate has a degree in Chemistry or Biology and substantial experience in a pharmaceutical quality control environment. This role offers a chance to work in a pioneering organization focusing on innovative medical solutions.