Process Validation Engineer- MSAT

ppbDuration: 1 year with extension possibility /b /p pAdryan is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the life sciences industry. We are specialised in the areas of project management, engineering, CQV and compliance. /p h3About the role /h3 pWe are looking for an Engineer – MSAT Validation to support validation and continuous improvement activities within a GMP manufacturing environment. /p h3Key Responsibilities /h3 ul liExecute and coordinate validation activities including cleaning, mixing, sterilization, and hold‑time studies. /li liAuthor and review validation protocols, reports, and risk assessments. /li liSupport process improvements, technology transfers, and new technology implementations. /li liCollaborate with Manufacturing, Quality, Engineering, and Project teams. /li liSupport investigations, CAPAs, change controls, and inspection readiness activities. /li /ul h3Requirements /h3 ul liBachelor's degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related field. /li li2+ years of experience in pharmaceutical, biotech, or biologics manufacturing. /li liExperience with validation, CQV, process validation, or equipment qualification (IQ/OQ/PQ). /li liKnowledge of GMP and pharmaceutical regulatory requirements. /li liStrong communication, problem-solving, and technical writing skills. /li /ul h3Preferred Qualifications /h3 ul liExperience in MSAT, technology transfer, biologics, vaccines, cell gene therapy, or sterile manufacturing. /li liLean/Six Sigma or continuous improvement experience. /li /ul /p #J-18808-Ljbffr