The role

We have a full-time, Microbiologist role available based at our site in Alnwick. This is a pivotal role working in a busy team. As the Microbiologist, you will:

• Develop, validate, and apply microbiological methodologies.

• Apply microbiological methodologies during the quality control and stability evaluation of a range of materials.
• Environmental monitoring of the GMP manufacturing facility and during the manufacture of sterile products.
• To comply & adhere to GxP guidelines and regulations as required of this role.

Main tasks and responsibilities

• As guided/requested, develop, validate, and report microbiological methodology.
• Apply microbiological methodologies during the quality control and stability evaluation of a range of materials.
• Participate in environmental monitoring of the GMP manufacturing facility and during the manufacture of products.
• Prepare work protocols for approval, critically assess data generated and review data from peers.
• Prepare and review reports, quality documents and training documentation.
• Acquire/record data in a manner that complies with GxP and internal policies/procedures.
• Perform assigned roles such as equipment responsible operator, equipment hardware/software validation and the ordering of consumable items.
• Work with due regard to health and safety of self and others.
• Work flexibly across the site to meet business needs.

Qualifications and experience required for competent performance

• BSc or equivalent in a relevant scientific discipline

• Experience in the application of microbiological methodologies in a pharmaceutical environment is advantageous.
• Good written and oral communication skills.
• The ability to critically assess data.
• Have a flexible approach to new work challenges.