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Validation Engineer
2 maanden geleden
Job Summary
Oxford Global Resources is seeking a highly skilled Validation Engineer to join our team in Tilburg. As a Validation Engineer, you will play a critical role in ensuring the validation status of equipment, processes, and cleaning procedures within our client's organization.
Key Responsibilities
- Develop and implement validation protocols for equipment, utilities, processes, cleaning, and computer validation, including reports and advice on periodic assessment frequencies.
- Write and review protocols for Process Performance Qualification (PPQ), cleaning validation, and Continued Process Verification (CPV).
- Provide technical support to other departments and ensure the validated status of all cGMP-critical automated process applications and quality systems.
- Stay up-to-date with current developments and regulations in the pharmaceutical industry.
- Validate SMEs for internal and external audits.
Requirements
- Bachelor's or university degree in a relevant field, such as technology, science, or a related field.
- 1-7 years of experience as a validation engineer in a matrix organization.
- Solid background in one or more areas involved, such as validation, GMP, and pharmaceutical production.
Benefits
- Year contract with Oxford Global Resources, with intention to extend or convert.
- Salary €4500 - €5500.
- Good secondary benefits.
Language
English (en-US)
