Lab Analyst - LCMS/MS

Synexa Life Sciences; Macclesfield; On-site; GBP 32,000 - 52,000; Full time

Job summary

Synexa Life Sciences is seeking a Lab Analyst (LC-MS/MS) to support bioanalytical studies and routine sample analysis in a regulated CRO setting. You will operate and maintain LC-MS/MS equipment, prepare study documentation, and ensure compliance with GxP/SOP requirements to deliver high-quality analytical data.

The role requires MSc in a scientific field (or 2–3 years in industry), hands-on LC/MS experience, and strong English communication for teamwork and study documentation.

Qualifications

• Hands-on experience with LC/MS.
• MSc in a scientific field, or 2–3 years of equivalent industry experience.
• Familiarity with advanced analytical instruments (e.g., LC/MS, microplate readers, flow cytometers, electrochemiluminescence analysers).
• Proficient in written and spoken English, with strong teamwork and negotiation skills.

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 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.
• Observe appropriate regulatory guidelines, SOPs, policies and study documentation.
• Work in accordance with SOPs by authoring, reviewing, and maintaining SOPs, guidance documents and policies, and providing training.

Skills

LC-MS/MS

Pipette handling

Lab techniques

Teamwork

English communication

Education

Master's degree in a scientific field

Tools

Centrifuges

Biosafety cabinets

Plate washers

Incubators

LIMS

Job description

We are seeking a Lab Analyst (LC-MS/MS) to support bioanalytical studies by performing routine sample analysis, sample preparation, and laboratory activities in a regulated CRO environment. The role involves operating and maintaining LC-MS/MS equipment, preparing study documentation, ensuring compliance with GxP and SOP requirements, and contributing to the delivery of high-quality, reliable analytical data.

Key Responsibilities

• 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.
• Observe appropriate regulatory guidelines, SOPs, policies and study documentation.
• Working in accordance with standard operating procedures (SOPs) by authoring, reviewing, and maintaining SOPs, guidance documents, and policies, as well as providing training and support to staff.

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.).
• Familiarity with advanced analytical instruments (e.g., LC/MS, microplate readers, flow cytometers, electrochemiluminescence analysers).
• Proficient in written and spoken English, with strong teamwork and negotiation skills.

Preferred

• Practical experience in GxP/GCLP-accredited environments.