Specialist, QA Documentation

We are looking for a motivated and highly organized Specialist, QA Documentation to join Glaxo Smith Kline's Quality Assurance team. In this role, you will be responsible for developing and maintaining quality assurance documentation for GSK's products. You will work closely with other QA professionals to ensure that all documents are accurate and up-to-date.To be successful in this role, you must have a degree in a related field, such as Science or Engineering, and at least three years of experience in a Quality Assurance role. You must have an eye for detail and the ability to identify errors and discrepancies in documents. Additionally, you must be comfortable working in a fast-paced environment and be able to manage multiple tasks at once.If you're an experienced QA professional with a passion for accuracy and an eye for detail, we'd love to hear from you.

According to JobzMall, the average salary range for a Specialist, QA Documentation in Cambridge, UK is £35,000-£45,000. This range may vary depending on the individual's experience and qualifications.

GlaxoSmithKline plc is a British multinational pharmaceutical company headquartered in Brentford, London. Established in 2000 by a merger of Glaxo Wellcome and SmithKline Beecham, GSK was the world's sixth largest pharmaceutical company as of 2015, after Pfizer, Novartis, Merck, Hoffmann-La Roche and Sanofi.