Quality Assurance Specialist / Manager

☞ VRS UK

View: 104

Update day: 07-05-2024

Location: Ripon Yorkshire and the Humber

Category: Quality Assurance / Quality Control

Industry: Research Biotechnology Pharmaceuticals

Position: Entry level

Job type: Full-time

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Job content

An exciting opportunity to join a specialist CRO as QA Manager. The company conducts an expanding range of studies to develop regulatory data to support the registration of biopesticides and low-risk crop protection products. Key responsibilities will include auditing all aspects of the GLP studies to ensure compliance with the guidelines and the integrity of the generated data. This role would suit an experienced quality assurance professional who is looking to join an ambitious yet very friendly team at a company with an amazing future. They have an excellent reputation for quality work in a highly niche area that has huge growth potential. You will be working alongside a highly supportive management team who will empower you to do what you are good at – ensure the compliance of the studies being conducted. For a more detailed job description and information about the recruiting company, please contact John Sherratt at VRS Regulatory quoting job reference VRSREG1793. Key Skills: Quality, quality assurance, quality audits, GLP, regulated research/studies, compliance, reports, procedures, data, record keeping. VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors
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Deadline: 21-06-2024

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