Senior Validation Analyst
6-7 Month Contract (potential for permanent)
Bristol
Immediate requirement
We are seeking a Senior Validation Analystto join our team inBristolon an initial6-to-7-month contract. This will be a PAYE contract via LiCa Scientific and well be acting as an Employment Business.
This is an urgent role, and we are looking for someone begin as soon as possible i.e. during October and promptly take ownership of important analytical validation projects. If you are skilled in HPLC method validation within a regulated environment, and available on these timescales we want to hear from you.
What You'll Do:
This role is focussed on ensuring the integrity and compliance of analytical methods. Key responsibilities will include:
Performing and overseeingmethod validationactivities, with a primary focus onHPLC.
Taking the lead on generating crucial documentation, including writingProtocols, Reports, Test Methods, and SOPs.
Thoroughly reviewing technical documentation such as protocols, validation reports, laboratory notebooks (paper or electronic), and raw analytical data.
Applying your strong technical knowledge of HPLC and, ideally, other techniques such as GC, KF, and FTIR to support the team.
Ensuring all validation activities strictly comply withGMP requirementsand relevant regulatory guidelines.
Your background:
Significanthands on experience in method validation, specifically with High Performance Liquid Chromatography (HPLC).
Essential previous experience working in aregulated laboratory environment (GLP/GMP).
Strong theoretical and practical understanding of analytical techniques (HPLC is essential; GC, KF, and FTIR knowledge is a plus).
Exceptional ability to write and review complex technical documents (protocols, reports, and methods).
A highlyorganised and methodicalapproach to work, coupled with excellent verbal and written communication skills.
On this occasion, LiCa Scientific is acting as an employment business.
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