Assistant Analyst - GLP

Tetra Tech Europe; Bedford; On-site; GBP 30,000 - 45,000; Full time

Job summary

Tetra Tech Europe in Bedford is seeking an experienced scientist to join its GLP analytical team on a full-time, permanent basis. You will assist with regulated analytical studies, routine lab activities, sample preparation, record keeping and compliance with GLP standards.

You will handle samples, calibrate equipment, prepare reagents and contribute to data entry, method validation, and collaboration with study directors and QA staff. Monday–Friday, 9:00–17:00 in Bedford.

Qualifications

• Minimum two years’ commercial laboratory experience, preferably in a GxP/GLP environment.
• Strong attention to detail and accurate record-keeping.
• Familiarity with analytical platforms (LC-MS/MS, HPLC, GC) and laboratory procedures.

Responsibilities

• Perform routine laboratory activities and sample preparation.
• Record, label, store and track study samples; ensure accurate contemporaneous records.
• Operate, calibrate and maintain laboratory equipment; support data entry and analysis.
• Assist in deviation investigations and compliance with GLP standards.

Skills

Attention to detail

Written communication

Verbal communication

Team collaboration

Organisational skills

Education

Bachelor's degree in Chemistry or related discipline

Tools

LC-MS/MS

HPLC

GC

Job description

Build Your GLP Analytical Career with Tetra Tech in Bedford

Purpose and Scope of the Role

Tetra Tech is seeking an experienced and detail-oriented scientist to join our GLP analytical team in Bedford. This is a full-time, permanent role supporting the delivery of regulated analytical studies through routine laboratory activities, study sample preparation, accurate record keeping and compliance with Good Laboratory Practice standards. You will receive, record, label, store and track study samples, prepare reagents, standards and quality control samples, and conduct routine laboratory procedures with a high degree of accuracy. You will also operate, calibrate and maintain laboratory equipment, support basic troubleshooting, process analytical results for entry into data spreadsheets, and work collaboratively with analysts, study directors and quality assurance personnel.

Your Impact in this Position

You will play an important role in ensuring regulated studies are delivered accurately, efficiently and in line with study protocols, SOPs and GLP requirements. You will help maintain high-quality laboratory records, support data completeness and compliance, and assist in the investigation of laboratory deviations and non-conformances. As you develop, you may support method validation, method transfer and study activities, including sample analysis by LC-MS/MS, GC-MS or other analytical platforms.

Core Capabilities

• GLP Laboratory Practice Perform sample preparation, extraction and routine laboratory activities in accordance with study protocols, SOPs and GLP requirements.
• Sample and Data Management Receive, record, label, store and track study samples, process analytical results and maintain accurate, contemporaneous records.
• Analytical Equipment and Techniques Operate, calibrate and maintain laboratory equipment, prepare reagents and standards, and support sample analysis using LC-MS/MS, GC-MS or other platforms.
• Quality, Compliance and Safety Review laboratory data and documentation, support deviation investigations, maintain housekeeping standards and follow health and safety requirements.
• Collaboration and Organisation Work independently and as part of a team, prioritising tasks, meeting deadlines and communicating effectively with laboratory, study and quality assurance colleagues.

Skills, Qualifications And Experience

You will have a BSc degree, or equivalent, in Chemistry, Analytical Chemistry, Biochemistry or a related scientific discipline, with a minimum of two years’ commercial laboratory experience, preferably within a GxP environment. You will have experience following laboratory procedures, maintaining accurate scientific records, strong attention to detail and good written and verbal communication skills. Knowledge of GLP, hands‑on sample preparation and extraction techniques, and familiarity with LC-MS/MS, HPLC, GC or similar platforms would be desirable.

Work Patterns and Location

This is a full-time, permanent role based at Tetra Tech’s Bedford laboratory working Monday – Friday, 9:00 – 17:00.

In alignment with the Equality Act 2010, we will make reasonable adjustments to support candidates and employees requiring additional arrangements. This could include adaptations to work schedules, training approaches, or the physical workspace. Please inform us if you need any accommodations during the recruitment process or in your day-to-day role.