QA Validation Officer
Biotechnology Clinical Life Sciences Pharmaceuticals
An exciting opportunity has become available for Quality Assurance Officer within a leading biopharmaceutical organisation, based in the Midlands. The role involves a range of QA and validation activities and performing internal and external compliance audits in accordance with QMS and Standard Operating Procedures (SOPs).
The ideal candidate will have previous exposure of QA validation within an GMP, ISO 13485 or related pharmaceutical or medical devices QA environment. Experience of root cause analysis, QMS, CAPA, validation, deviations and calibration, and familiarity of electronic QMS systems would be highly desirable, particularly with FDA Part 820.
You’ll contribute to the development, implementation and maintenance of quality assurance and quality improvement systems and policies to ensure compliance with relevant regulatory requirements, as well as participating in QA aspects of corrective action and/or change control requests. Knowledge or a background from a QC laboratory setting is also highly desirable.
The company has easy access via road network and good public transport links, offering competitive benefits, and are looking for people who are keen to grow and develop within the organisation.