LBA Scientist (Lab Analyst role)

Role Overview
We are seeking a Scientist (LBA) to perform bioanalytical and Ligand Binding Assay (LBA) activities in a regulated CRO environment. In this role, you will execute routine sample analysis, method validation, and laboratory activities in compliance with GxP requirements, SOPs, and applicable regulatory guidelines, while ensuring the generation of high-quality and reliable data.
As a study-specific analyst, you will operate and maintain laboratory equipment, prepare and review study documentation, manage laboratory consumables and LIMS records, and support assay troubleshooting and continuous improvement initiatives. You will also contribute to SOP authoring and review, maintain accurate task and time records, support the training of new staff, and ensure adherence to quality, health and safety, and regulatory requirements at all times.
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
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.

Employment type
Full-Time

Work arrangement
No