Process Validation Engineer- MSAT
Adryan
Role description
Duration: 1 year with extension possibility
Adryan 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.
About the role
We are looking for an Engineer – MSAT Validation to support validation and continuous improvement activities within a GMP manufacturing environment.
Key Responsibilities
- Execute and coordinate validation activities including cleaning, mixing, sterilization, and hold‑time studies.
- Author and review validation protocols, reports, and risk assessments.
- Support process improvements, technology transfers, and new technology implementations.
- Collaborate with Manufacturing, Quality, Engineering, and Project teams.
- Support investigations, CAPAs, change controls, and inspection readiness activities.
Requirements
- Bachelor's degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related field.
- 2+ years of experience in pharmaceutical, biotech, or biologics manufacturing.
- Experience with validation, CQV, process validation, or equipment qualification (IQ/OQ/PQ).
- Knowledge of GMP and pharmaceutical regulatory requirements.
- Strong communication, problem-solving, and technical writing skills.
Preferred Qualifications
- Experience in MSAT, technology transfer, biologics, vaccines, cell & gene therapy, or sterile manufacturing.
- Lean/Six Sigma or continuous improvement experience.
