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Adryan

The Netherlands / Global

Process Validation Engineer- MSAT

Job 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.

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