Validation Specialist (GMP) – Process & Cleaning Validation (Part-Time) | Mitarbeiter Validierung (GMP) – Prozess‑ & Reinigungsvalidierung (m/w/d), mind. 60%
WALA Heilmittel GmbH
Job Summary
This role involves joining the Validation team at WALA, a foundation-led company focusing on sustainable economics and a collaborative culture. The specialist will be crucial in ensuring safe and reliable pharmaceutical manufacturing processes by planning, coordinating, executing, and documenting process and cleaning validations across various production areas. Key responsibilities include ensuring timely and GMP-compliant implementation of all validation activities according to the Master Plan, evaluating process implementations, and conducting performance qualifications (PQ) for new machinery. The ideal candidate holds a natural science degree (e.g., Pharmacy, Pharmaceutical Technology) or a relevant technical/scientific qualification with professional experience in a GMP environment. This position requires strong analytical skills, precise documentation abilities, and the capacity to work independently within an interdisciplinary team, contributing directly to continuous process safety and quality assurance.
Required Skills
Education
Completed natural science degree (e.g., Pharmacy, Pharmaceutical Technology) or technical/scientific qualification (e.g., Pharmaceutical Technician, Chemical Technical Assistant, Pharmaceutical Technical Assistant)
Experience
- Professional experience in a GMP environment (required if educational background is a technical/scientific apprenticeship)
- Routine handling of GMP-compliant documentation
- Experience in planning, coordination, and execution of validation activities
Languages
Additional
- Temporary contract for a maternity and parental leave replacement (initially limited to one year); Minimum 60% working hours required; Ability to work remotely up to 40% of contracted working time.
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