Scientist - LCMS/MS

Synexa Group; Macclesfield; Hybrid; GBP 36,000 - 60,000; Full time

Job summary

Synexa Life Sciences (Pty) Ltd. is seeking a Scientist to support bioanalytical studies by performing analyses, maintaining instruments, and preparing documentation in line with GxP and SOPs.

The role includes contributing to method development, ensuring regulatory compliance, and supporting training and project delivery as a study-specific analyst.

Qualifications

• Hands-on experience with LC/MS and routine lab practices.
• MSc in a scientific field or 2–3 years of equivalent industry experience.
• Fluent English with strong teamwork and communication skills.

Responsibilities

• Perform bioanalytical methods in line with GLP, GCP, GMP and SOPs.
• Maintain lab instruments and environment per SOPs.
• Prepare documentation, reports and study manuals.
• Write and review SOPs and support method documentation.
• Train new personnel as needed.
• Record tasks and time in the logging system.
• Ensure regulatory compliance and staff training.

Skills

LC/MS experience

Pipette handling

Analytical techniques

Teamwork

English communication

Education

MSc in a scientific field

2–3 years industry experience

Tools

LC/MS

Job description

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 & 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.

Desirable:

• Practical experience in GxP/GCLP-accredited environments.