An exciting opportunity has arisen for an early career Scientist or Quality professional to join an expanding GMP pharmaceutical testing company!
You will work across multiple departments within a well-established facility, ensuring GMP compliance of laboratory studies and equipment. The role will involve creating and reviewing quality documents within the Quality Management System, monitoring validation protocols and routine checking of analytical data. You will work closely with different teams, utilising your excellent interpersonal skills to build rapport, facilitating seamless communication across the site.
Qualifications/Skills/Experience required:
* Minimum 12 months relevant experience in a GxP regulated environment
* Excellent communication skills and attention to detail is essential
* Ability to interpret technical documents (project plans, stability protocols, analytical methods)
* Experience in deviations, change control, audits and CAPA’s is desirable
Applications are also invited from Analytical chemists who have experience within a GMP laboratory, who are seeking a move into Quality Assurance.
Apply today to be considered!
Key words: quality, audit, quality management systems, auditing GxP, GMP, GCP, GLP, FDA, ISO, regulations, deviations, risk assessment, CAPA, Auditor, Cambridgeshire, East Anglia, South East, Hitchin, Letchworth Garden City, Bedford, Stanstead, Bishop’s Stortford, Cambridge, VRS8769AW
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