GFR Analytical Services
Laboratory Analyst
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Company Description
GFR Analytical Services (UK) is an MHRA-approved contract testing laboratory serving the healthcare, Pharmaceutical, and food supplement sectors. The company provides analytical testing and consultancy services, with a strong focus on GMP QC batch release testing and method development and validation.
GFR Analytical Services also offers stability testing and storage in line with ICH guidelines, as well as raw material characterization and troubleshooting support. The team supports clients with prototype and lab-scale formulation preparation, and comprehensive Analytical CMC and QC services, creating a dynamic environment for laboratory professionals.
Role Description
The Laboratory Analyst is a full-time, on-site role based in Blackburn. This role is responsible for performing routine and non-routine analytical testing on a variety of samples in accordance with GMP, MHRA, and internal quality standards. Daily activities include:
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- Operating and maintaining laboratory equipment
- Preparing reagents and samples
- Documenting test results accurately
- Supporting method development, validation, and stability studies
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The Laboratory Analyst will contribute to QC batch release testing, assist in troubleshooting analytical issues, and collaborate with seniors to ensure timely, reliable data for client projects while adhering to safety procedures, participation in internal audits, and continuous improvement of laboratory processes.
Qualifications
- Strong analytical skills for data interpretation, problem-solving, and troubleshooting across a range of tests and methods.
- Hands-on experience with laboratory equipment, including setup, routine operation, maintenance, and basic calibration.
- Core laboratory skills, such as sample preparation, reagent handling, method execution, and compliance with safety and GMP practices, predominantly with HPLC.
- Relevant scientific degree (e.g., Chemistry, Pharmaceutical Sciences, Biochemistry) or equivalent laboratory experience in a GMP/ MHRA-regulated setting.
- Strong attention to detail, effective written and verbal communication, and the ability to follow SOPs and regulatory guidelines.
- Ability to work collaboratively in a cross-functional team, manage multiple tasks, and meet project timelines.
- Experience in pharmaceutical testing, and familiarity with ICH stability guidelines, is advantageous.
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