About this role
Role Overview
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.
PLEASE ENSURE THAT YOUR CV/RESUME IS SUBMITTED IN ENGLISH.