Scientist - LCMS/MS

Synexa Life Sciences; Macclesfield; On-site; GBP 32,000 - 44,000; Full time

Job summary

Synexa Life Sciences seeks a Scientist to support bioanalytical studies, perform analyses, and maintain lab instruments in compliance with GxP and SOPs. The role includes method development support, ensuring regulatory compliance and contributing to training and project delivery.

Key responsibilities include performing GLP/GCP/GMP-compliant analyses, documenting work according to SOP standards, and maintaining instruments and LIMS records.

Qualifications

• Hands-on LC/MS experience in a regulated setting.
• MSc in a scientific field or 2–3 years of equivalent industry experience.
• Experience with GxP/GCLP environments and SOP adherence.
• Proficient English, strong teamwork and negotiation skills.
• Experience with documentation, pipetting and basic lab equipment.

Responsibilities

• Perform bioanalytical methods in line with GLP, GCP, GMP and SOPs.
• Document all work according to GxP and SOP standards.
• Operate and maintain laboratory instruments and environment 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 & 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 and staff training.

Skills

LC/MS experience

English proficiency

Teamwork & negotiation

Education

MSc in a scientific field

Tools

Centrifuges

Biosafety cabinets

Plate washers

Incubators

Job description

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 & 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 & 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 & 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.
• Practical experience in GxP/GCLP-accredited environments.