Prepare and check data accurately according to company, customer and regulatory requirements.
Verify the quality and accuracy of results for material to meet pre-defined acceptance criteria.
Take a lead role in the batch/job approval process.
Managing site Continuous Improvement (CI) and improvement initiatives.
Responsible for assigned items of Laboratory equipment and instrumentation or 5S standards (as an expert user, resolving issues and promoting best practice).
Take a lead role in provision of training for New Starters, and for Microbiologists in areas of expertise.
Responsible for the safety of self and others within the Laboratory.
Carry out testing using appropriate aseptic techniques.
About You:
This role would suit a motivated person who has strong experience of working in a GMP (Quality) environment. Strong people skills and a proven ability to work in a team (eg; flexible approach, good communication, planning and organizational skills) as well as good report writing skills. You should have knowledge/experience of microbiology laboratory testing techniques, ideally within a GMP environment (eg; knowledge of the microbiological requirements for non-sterile pharmaceutical manufacture). An excellent understanding and appreciation of the testing of raw materials and final product, as well as environmental and water testing is important. You will also have a strong continuous improvement mindset and a willingness to work towards standardised and lean working practices.