Job Description:
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
Follow VRS Recruitment on LinkedIn to view all our latest vacancies!
Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
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
Follow VRS Recruitment on LinkedIn to view all our latest vacancies!
Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.
Job number 1412333
metapel
Company Details:
VRS
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