i-Pharm Consulting
Jobid=A.0.174
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.
