QC Microbiology Lab Technician

Kindeva Drug Delivery

Our Work Matters:

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make:

Working within our Microbiology Team you will be responsible for the testing of pharmaceutical raw materials (including components), intermediates and finished products for batch release, stability, development studies and customer complaints in line with site procedures.

You will be pivotal in the completion of site support activities including Environmental monitoring, water analysis and microbial identification analysis, and play a key part in representing the department with our external customers and regulators.

• Knowledge and application of current safety regulations (e.g., CoSHH) as applicable to laboratory functions.
• Work to appropriate laboratory systems, standards and procedures.
• Complete analytical documentation including the input of results onto the LIMS system.
• Awareness of current regulatory standards as applicable to laboratory functions.
• Work to GMP/GLP standards and principles and maintain good laboratory housekeeping.
• Perform microbiological testing using methods to meet scheduled timelines.
• Have a sound knowledge of pharmaceutical products and testing.
• Develop an understanding of the tests carried out and their impact on the products/materials worked on.
• Support continuous improvement activities within own group.
• Participate as a team member for Group CI projects as appropriate.
• Have a basic understanding of the resources required to perform laboratory-based activities.

Additional Information:

Working Hours: 37.5hrs per week

Location: Derby Road, Loughborough

• Ideally degree qualified in a relevant scientific discipline with practical laboratory elements.
• 1+ years' experience of working within a GMP laboratory environment is required or 2+ years' experience of working within a non-GMP laboratory is preferable.
• Previous hands-on experience of aseptic techniques is preferable.
• Knowledge of pharmaceutical testing requirements, testing equipment and current microbiological techniques is preferable.
• Previous experience working with GLP, GMP, Specifications and Test Methods is preferable.
• Computer literate, familiar with Microsoft Word and Excel.

Key Capabilities:

• Good organisational, interpersonal, and time management skills
• Enthusiastic, flexible, conscientious and proactive in approach
• Take a positive approach to own training and development
• Good problem-solving skills
• Strong verbal and numerical aptitude skills
• Good communication skills
• Strong team player with the ability to work independently