Join the team as a Cleaning Validation Engineer and play a crucial role in ensuring high-quality standards in pharmaceutical manufacturing. You will focus on preparing and updating cleaning validation documents, supporting audits, and facilitating the introduction of new products and equipment. Collaborate with cross-functional teams to improve compliance and operational excellence. Enjoy working in a dynamic environment where your communication and project management skills will shine. Read on to discover what challenges await you.

Over het bedrijf

Panda International

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Job Role: Cleaning Validation Engineer

About the Role:
We are seeking an experienced Cleaning Validation Engineer to join our Manufacturing Science and Technology (MSAT) team. This role focuses on cleaning validation in pharmaceutical manufacturing, ensuring processes meet strict quality and regulatory standards. You will manage validation activities, documentation, audits, and support the introduction of new products and equipment, contributing to compliance and operational excellence.

Key Responsibilities:

Prepare and update cleaning validation documentation, including protocols, reports, and studies.
Gatekeep proposed changes and prioritize cleaning validation projects.
Support audits and ensure timely responses to findings.
Facilitate the introduction of New Product Introductions (NPI) and new equipment in the validation program.
Report incidents, deviations, and propose solutions to improve compliance.
Collaborate with cross-functional teams, including manufacturing, quality, and engineering.

Key Competencies:

Strong expertise in API manufacturing processes and cleaning validation.
Solid understanding of validation principles and statistical methods.
Knowledge of Quality & Compliance/regulatory requirements (GMP) in cleaning validation.
Project management, planning, organization, and coordination skills.
Ability to manage complexity, deadlines, and competing priorities.
Excellent communication and interpersonal skills, able to interact at different organizational levels.
Familiarity with systems such as eLIMS, truVAULT, COMET, PRX, CRB, SAP, PASx, Minitab, CPV Automation (preferred).

Requirements:

Master’s Degree in (Bio)Sciences or Life Sciences.
Fluency in Dutch and English.
2–4 years of relevant work experience in pharmaceutical manufacturing or validation.

Practical’s:

Location: Geel, Belgium
Duration: 12+ months
Start Date: ASAP
Work Model: Full-time, On-site

Interested or know someone who might be?
Send your CV or inquiries to via de button "Solliciteer nu" op deze pagina. to apply or learn more.

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