Engineer MSAT Validation

Supporting Technical Operations Leaders to Build High-Performing Biopharma Teams | Recruitment Consultant @ Panda

Job Description

The Manufacturing Science & Technology (MSAT) department is the leading partner in supporting process validation, technical product ownership, and a key driver of sophisticated technologies. You will drive technologies that enable high-value patient care at a growing biotherapeutic drug substance site.

In this role, you will focus on the validation of supporting processes (cleaning, mixing, sterilization, and holding time), while driving process improvements and new technology deployment. You will be responsible for planning and executing validation activities, maintaining compliance, and ensuring audit readiness through rigorous documentation and stakeholder communication.

Education:

Bachelor’s degree (or equivalent) in a Science, Engineering, or Technical subject.

Experience:

Minimum of 4 years of relevant experience in the (bio) pharmaceutical industry or related academic experience.

Core technical expertise:  Knowledge of regulatory requirements and industry guidelines (FDA, EMA, ICH, ASTM, ISO, ISPE, PDA).

Required hands‑on skills:  Writing and reviewing validation protocols/reports; planning and coordinating validation studies.

Required scientific/technical knowledge:  Understanding of risk management, root‑cause problem solving, and Good Documentation Practices (GDP).

Preferred Requirements

Additional experience:  Previous experience in a Manufacturing Science & Technology (MSAT) environment.

Advanced technical skills:  Proficiency in 6‑Sigma/Lean or similar continuous improvement methodologies.

Specific technologies or platforms:  Experience in cleaning validation, mixing validation, sterilization qualification, or holding time studies.

Industry or domain exposure:  

Experience with biotherapeutic drug substance manufacturing.

Soft skills or certifications:  Strong stakeholder management and communication skills.

Practicalities

Start Date:

January 1, 2026

Contract Duration:  12 Months

Location:

Leiden, the Netherlands

Additional:  40 hours per week; competitive hourly rate.

Interested?

Interviews and offers can move quickly. Send your CV to Oluali Titelman at  or call +31 (0) today to secure your spot in the process.

Seniority level:

Mid‑Senior level

Employment type:

Full‑time

Job function:

Manufacturing, Science, and Strategy/Planning

Industries:

Biotechnology Research and Pharmaceutical Manufacturing

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