Cleaning Validation Engineer
About the job:
Design, plan and execute cleaning and process validation activities in accordance with regulations and guidelines
Ensure the follow-up of the cleaning validation and the cleaning cycle development in a regulated environment
Participate in the creation and the implementation of the cleaning validation strategy
Execute cleaning validation tests in accordance with approved protocols, procedures and guidelines
Write process and cleaning validation final reports that offer conclusions based on test results
Analyze data and provide recommendations for improvements in cleaning / manufacturing process, and equipment Clean In Place (CIP)
Provide technical leadership for deviation investigations related to cleaning validation activities (residual product/detergent and microbial contamination issues)
Write technical cleaning evaluations as requested, including calculations, and deviations with root cause and impact assessment
Generate the closure and validation report for cleaning validation of various equipment systems
About you:
Degree in pharmaceutical sciences, chemical engineering, microbiology, or a related field
Minimum 3 years of experience in cleaning validation within a GMP-regulated environment
Strong understanding of cleaning chemistry, residue limits, analytical methods, and equipment design
Knowledge of applicable regulatory guidance (FDA, EMA, PIC/S, ISPE, etc.)
Experience with risk-based approaches and tools (e.g., FMEA, risk assessments)
Excellent technical writing and communication skills
Proficient in English and French. German is a plus
About us:
Human-sized company with great colleagues from a large diversity of cultural and professional backgrounds
We do care about our people, communicate openly and value feedback
Work as a team where every member is valued and appreciated
Opportunity to contribute to ambitious projects within an international and multicultural environment that fosters innovation, collaboration, and professional growth
Continuous learning and development opportunities via internal or external training and workshops
Competitive salary package in line with industry practice together with exceptional employment benefits
At GXP Consulting Switzerland everyone contributes to our joint success and grows individually!
If you also share the same passion and values, we will be glad to hear from you! Please send us your application.
By Mail Biopôle – Metio Batiment Route de la Corniche 2 CH-1066 Epalinges Switzerland Tel:+41 21 510 3157
Experts for Life Sciences industries.
Memberships and/or partnerships Contact us at contact@gxp-cs.com
#J-18808-Ljbffr
About the job:
Design, plan and execute cleaning and process validation activities in accordance with regulations and guidelines
Ensure the follow-up of the cleaning validation and the cleaning cycle development in a regulated environment
Participate in the creation and the implementation of the cleaning validation strategy
Execute cleaning validation tests in accordance with approved protocols, procedures and guidelines
Write process and cleaning validation final reports that offer conclusions based on test results
Analyze data and provide recommendations for improvements in cleaning / manufacturing process, and equipment Clean In Place (CIP)
Provide technical leadership for deviation investigations related to cleaning validation activities (residual product/detergent and microbial contamination issues)
Write technical cleaning evaluations as requested, including calculations, and deviations with root cause and impact assessment
Generate the closure and validation report for cleaning validation of various equipment systems
About you:
Degree in pharmaceutical sciences, chemical engineering, microbiology, or a related field
Minimum 3 years of experience in cleaning validation within a GMP-regulated environment
Strong understanding of cleaning chemistry, residue limits, analytical methods, and equipment design
Knowledge of applicable regulatory guidance (FDA, EMA, PIC/S, ISPE, etc.)
Experience with risk-based approaches and tools (e.g., FMEA, risk assessments)
Excellent technical writing and communication skills
Proficient in English and French. German is a plus
About us:
Human-sized company with great colleagues from a large diversity of cultural and professional backgrounds
We do care about our people, communicate openly and value feedback
Work as a team where every member is valued and appreciated
Opportunity to contribute to ambitious projects within an international and multicultural environment that fosters innovation, collaboration, and professional growth
Continuous learning and development opportunities via internal or external training and workshops
Competitive salary package in line with industry practice together with exceptional employment benefits
At GXP Consulting Switzerland everyone contributes to our joint success and grows individually!
If you also share the same passion and values, we will be glad to hear from you! Please send us your application.
By Mail Biopôle – Metio Batiment Route de la Corniche 2 CH-1066 Epalinges Switzerland Tel:+41 21 510 3157
Experts for Life Sciences industries.
Memberships and/or partnerships Contact us at contact@gxp-cs.com
#J-18808-Ljbffr
Cleaning Validation Engineer Arbeitgeber: Gxp Consulting Switzerland
GXP Consulting Switzerland ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern nicht nur ein wettbewerbsfähiges Gehalt bietet, sondern auch vielfältige Entwicklungsmöglichkeiten in einem dynamischen und kooperativen Umfeld. Unsere Unternehmenskultur fördert Teamarbeit und Innovation, was es Ihnen ermöglicht, Ihre Fähigkeiten als CSV Validation Engineer in der pharmazeutischen und biotechnologischen Branche weiterzuentwickeln und einen bedeutenden Beitrag zu leisten.
Kontaktdaten:
Gxp Consulting Switzerland Recruiting-Team
