Descripción de la oferta
Overview
QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Cleaning validation.
What you’ll be doing
You learn to develop and implement validation strategies following internal procedures and industry regulations.
Drafting and executing cleaning validations protocols (IQ, OQ, PQ) for manufacturing equipment (reactors, mixers, tanks, filling lines, autoclaves, refrigerators, incubators, etc).
Reporting on validation results and preparing summary reports.
Contribute to risk assessments related to cleaning procedures and equipment design.
Identify, document and investigate deviations; support the definition and follow-up of corrective and preventive actions (CAPAs).
Participate in periodic reviews and revalidation activities for cleaning procedures.
You provide support during internal and external audits, gaining valuable exposure to industry best practices.
Uphold a culture of knowledge sharing and continuous learning within the validation team.
What you bring
Education: Technical background (Chemistry, Engineering, Biotechnology, etc.)
Experience: At least 1 year of experience in qualification and validation.
Languages: Good level of English to draft and interpret technical documentation.
Who you are
You’re resilient and tackle challenges with a positive mindset.
You’re curious and always up for learning something new.
You have a no non-sense approach, honest, clear, respectful.
You’re innovative and bring ideas, not just opinions.
And above all, you’re serious about your work, but not too serious about yourself.
Send us your CV and motivation letter. You could be the next one to join the QbD family.
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