standards. Qualifications: Minimum of a Bachelor's degree in Engineering or related technical field. Proven experience as a CQV Engineer in the pharmaceutical or biotechnology industry. Strong understanding of industry regulations and guidelines. Excellent technical writing and communication skills. Ability to work independently as well as part of a team. more »
Cheshire, Chester, North West Hybrid / WFH Options
Real Staffing
embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across 3-5 days Location: Wilmslow - hybrid working Length - 6 months IR35 - Outside Please more »
to ISO or FDA regulatory standards is desirable Experience in calibration and/or maintenance support is ideal for a pharmaceutical, medical device, or biotech manufacturing company, or equivalent, with demonstrated skills in writing complex calibration SOPs and technical operating procedures Good planning skills to produce project timelines, good with more »
