Analytical Lab Technician – Method Validation

Lonza; Slough; On-site; Confidential; Full time

Benefits offered by this job

Dynamic culture

Inclusive workplace

Benefits package

Job summary

Lonza in Slough is seeking a Lab Technician (Method Validation) to support laboratory scientists by maintaining stock of reagents, consumables and buffers, and by upholding high standards to ensure a safe, organised and compliant working environment.

In this hands-on role you will perform housekeeping, prepare buffers, manage inventory on the WMS, order supplies, handle deliveries, plan tasks to schedule, and contribute to 6S and IMS initiatives while complying with cGMP.

Qualifications

• College qualification in a quality-related discipline.
• Willingness to learn from experience and adapt to change.
• Able to view errors as learning opportunities and take on new challenges.
• Commitment to process improvement and problem solving.

Responsibilities

• Perform housekeeping, routine instrument maintenance, and monitor stock levels to ensure uninterrupted operations.
• Prepare analytical buffers following laboratory methods and processes.
• Manage consumables inventory and stock locations based on lifecycles.
• Order reagents via WMS or external suppliers to maintain stock levels.
• Process department deliveries with proper storage and notification to stakeholders.
• Plan and complete tasks within agreed timelines and quality standards.
• Support 6S and IMS initiatives for an organised, compliant lab.
• Maintain GMP training per defined plans.
• Adhere to cGMP standards and lab procedures.

Job description

Lonza in Slough is seeking a Lab Technician (Method Validation) to support laboratory scientists by maintaining stock of reagents, consumables and buffers, and by upholding high standards to ensure a safe, organised and compliant working environment.

In this hands-on role you will perform housekeeping, prepare buffers, manage inventory on the WMS, order supplies, handle deliveries, plan tasks to schedule, and contribute to 6S and IMS initiatives while complying with cGMP.