Highly rewarding opportunity for an experienced Quality professional!
Do you have 2-3 years’ experience working in a Quality role in the Pharmaceutical and/or Contract Research industries? Do you have a good understanding of ISO17025 and GCP regulations? Are you seeking a contract role in the Manchester area? Then this could be the role for you!
Using your previous experience, you will play a key role in development of the Quality system and identification of areas for Continuous Improvement and Corrective Actions. You will conduct compliance audits of complex information as well as leading and participating in internal and external audits as required. Using your excellent communication skills, you will lead Quality meetings and management reviews of the Quality system.
To be considered for this position you must have at least 2 years’ experience in a Quality role in the Pharmaceutical and/or Contract Research industry with a solid understanding of ISO17025 and GCP regulations.
Apply to VRS today to be considered for this fulfilling new role!
Key words: QA, quality assurance, auditor, specialist, quality management, continuous improvement, ISO17025, GCP, good clinical practice, Q-Pulse, Agile, CAPA, OOS, pharmaceutical, contract research, regulatory, regulations, validation, Manchester, Liverpool, North West, VRS5685LC
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