Scientist - LCMS/MS

Instruct-ERIC; Macclesfield; On-site; GBP 32,000 - 52,000; Full time

Job summary

Synexa Life Sciences is seeking a Scientist to support bioanalytical studies using LC/MS/MS in a GLP/GCP/GMP environment. The successful candidate will maintain instruments, document work in accordance with SOPs, and contribute to method development and project delivery.

Requirements include a master’s degree in a scientific field (or 2–3 years of equivalent experience), hands-on LC/MS experience, and strong teamwork and English communication skills.

Qualifications

• Master’s degree in a scientific field or 2–3 years of equivalent industry experience.
• Hands-on experience with LC/MS and routine analytical techniques.
• Familiarity with GLP/GxP regulatory environments is a plus.

Responsibilities

• Perform bioanalytical analyses using LC/MS in line with GLP, GCP, GMP, and SOPs.
• Maintain and operate laboratory instruments and the LIMS records.
• Prepare project-related documentation, including reports and SOPs.
• Ensure regulatory compliance and contribute to method development.
• Train new personnel and support study delivery.

Skills

English proficiency

Teamwork

Negotiation skills

Pipette handling & lab techniques

Education

Master’s degree in a scientific field

2–3 years of equivalent industry experience

Tools

LC/MS

Job description

Jobs in Structural Biology and Related Fields

Scientist - LCMS/MS

Macclesfield, Cheshire, United Kingdom

Synexa Life Sciences is a biomarker and bioanalytical lab contract research organisation (CRO), specialising in the development, validation and delivery of a wide range of complex and custom-designed assays.

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.

The role:

• 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.
• 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.