Validation Specialist
3 weken geleden
Are you a skilled validation engineer looking for a new challenge in a company that values individual growth and effort? We are seeking a talented professional to join our team at Oxford Global Resources in Tilburg.
Job Description:As a validation engineer, you will be responsible for performing process, cleaning, equipment validation, and Continuous Process Verification (CPV) tasks. You will also support critical projects for the organization.
Key Responsibilities:- Co-draft User Requirement Specifications (URS) within a multifunctional team and with suppliers
- Design and implement protocols for C&Q/IQ/OQ/PQ covering equipment, utilities, processes, cleaning, and computer validation
- Write protocols for PPQ, cleaning validation, and Continued Process Verification (CPV)
- Provide validation technical support within other departments
- Draft, review, and implement procedures and other controlled documents
- Stay informed of current developments and regulations for the pharmaceutical industry
- Validation of SMEs for internal and external audits
- Ensure the validated status of all cGMP-critical automated process applications and quality systems
- Bachelor's or university degree in a relevant field (e.g., technology, science, or 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
- Year contract via Oxford Global Resources, with intention to extend/convert
- Salary €4500 - €5500
- Good secondary benefits
Please note that visa sponsorship is not possible for this role. Only candidates with a working permit to live and work in the Netherlands should apply.
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