Role Overview
The Scientist will support bioanalytical studies by performing analyses, maintaining lab instruments, and preparing documentation in compliance with GxP and SOPs. The role also includes contributing to method development, ensuring regulatory compliance, and supporting training and project delivery.

Main Areas of Responsibility

• Perform bioanalytical methods in line with GLP, GCP, GMP, and SOPs.
• Perform routine analyses and document all work according to GxP and SOP standards.
• Operate and maintain laboratory instruments and environment as per SOPs.
• Prepare project-related documentation, including lab manuals and reports.
• Write and review SOPs and support method documentation.
• Manage consumables, monitor stock levels, and maintain LIMS records.
• Ensure compliance with health and safety guidelines and regulatory standards.
• Act as Study specific analyst on assigned projects.
• Train new personnel within area of responsibility when needed.
• Record tasks and time accurately in time logging application.
• Ensure compliance with regulatory guidelines by maintaining SOPs, policies, and study documentation, and providing staff training and support.

Qualifications and Experience
Required:

• Hands-on experience with LC/MS
• Master's degree (MSc) in a scientific field, or 2–3 years of equivalent industry experience.
• Skilled in analytical techniques and routine lab practices, including pipette handling, protocol adherence, and use of basic lab equipment (centrifuges, biosafety cabinets, plate washers, incubators etc.).
• Proficient in written and spoken English, with strong teamwork and negotiation skills.

Desirable:

• Practical experience in GxP/GCLP-accredited environments.

Please ensure that your CV/resume is submitted in English.

Location: Macclesfield, Cheshire
Department: Study Delivery
Employment Type: Full-Time
Minimum Experience: Experienced

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