Validation Engineer

2 maanden geleden

Tilburg, Nederland Oxford Global Resources Voltijd

Are you an experienced validation engineer, looking for your next career adventure within a company that values individual effort and growth? Then apply now for this challenging position for our client in Tilburg

Job description

As validation engineer you will perform process, cleaning, equipment validation and Continuous Process Verification (CPV) tasks and will support critical projects for the organisation. The validation department plays a key role in this by coordinating, planning, completing and reporting equipment, cleaning and process validation work. This department works closely with the development, quality and production departments and ensures the validation status of both existing and new processes and equipment involved in all investment projects.

Responsibilities

  • Co-drafting 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, including reports and advice on periodic assessment frequencies
  • Write protocols for PPQ, cleaning validation and Continued Process Verification (CPV).
  • Write periodic validation reports for critical equipment/facilities/processes, including Continuous 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.


Profile

  • A bachelor's or university degree in one of the target areas for the position (e.g., technology, science, or related field)
  • 1-7 years of working as a validation engineer within a matrix organization
  • Solid background in one or more of the areas involved such as validation, GMP and pharmaceutical production.

Benefits

  • Year contract via Oxford Global Resources, with intention to extend/convert
  • Salary €4500 - €5500
  • Good secondary benefits
  • Region Tilburg
  • Vacaturenummer: 24230

IMPORTANT NOTE: Visa sponsorship is not possible for this role, please do not apply if you do not have a working permit to live and work in the Netherlands. Your application will not be processed.

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