Overview
Validation Engineer Jobs in Limburg, Netherlands at i-Pharm Consulting
Title: Validation Engineer
Company: i-Pharm Consulting
Location: Limburg, Netherlands
Title: Validation Engineer
Contract Duration: 12 Months
Location: Netherlands
Are you looking for way to make real change? As a Validation Engineer, you will play a critical role in ensuring equipment, systems, and processes meet regulatory and quality standards.
You’ll be responsible for qualification, validation, and compliance activities, working closely with cross-functional teams to maintain operational excellence.
This is a great opportunity for an experienced validation professional with a background in pharmaceutical or food manufacturing, looking to apply their expertise in a fast-paced, high-performance environment.
Key Responsibilities
Develop and execute validation protocols (IQ, OQ, PQ) for equipment, systems, and processes.
Ensure compliance with industry regulations, including cGMP, FDA, and ISO standards.
Conduct risk assessments and gap analyses to identify and mitigate validation risks.
Document validation activities, maintaining accurate records and reports.
Support continuous improvement initiatives by optimizing validation processes and strategies.
Collaborate with engineering, production, and quality teams to ensure validation requirements are met.
Requirements
Experience in validation within a pharmaceutical manufacturing environment.
Strong knowledge of validation protocols, regulatory guidelines, and industry best practices.
Familiarity with cGMP, FDA, and ISO compliance requirements.
Hands-on approach with strong problem-solving and analytical skills.
Ability to work collaboratively in a fast-paced, regulated environment.
