Summary
Paul Bonijol is a Pharm.D. and biomedical engineer with 11 years' experience specializing in qualification, commissioning and validation of sterile injectable manufacturing and cleanroom systems across pharma and radiopharma sites. Based in Sierre, Switzerland, he has led CQV programs for complex aseptic equipment — from robotic bottle fillers and RABS to shockfreezers and depyrogenation tunnels — and coordinated multidisciplinary suppliers, software changes and regulatory audits. His background as a production pharmacist and vaccines batch release qualified person gives him rare cross-functional fluency between GMP quality, laboratory analytics and engineering. He has managed teams, updated validation strategies for regulatory compliance, and implemented image-analysis and automation proofs-of-concept in Python/ImageJ earlier in his career. Known for practical problem-solving under night-shift production constraints, he combines hands-on technical commissioning with strong documentation and audit readiness.
11 years of coding experience
3 years of employment as a software developer
Engineer's degree, Biomedical engineering, Obtained, Engineer's degree, Biomedical engineering, Obtained at Polytech'Lyon (École Polytechnique Universitaire de Lyon)
First year Master's (BSc) degree in biomedical research, Engineering for medicine and healthcare, Obtained, First year Master's (BSc) degree in biomedical research, Engineering for medicine and healthcare, Obtained at Université Claude Bernard (Lyon I)
French, english (toeic : 965/990, 2014 ; toefl ibt : 99/120, 2016), German