Did you ever want to work for a company placing human at the heart of its DNA? Are you ready to make a difference? Do you feel excited about the opportunity to collaborate and share your expertise with our industry leaders? YES? SO DO WE!
GXP CONSULTING Switzerland is a Swiss company with a passionate team of Life Sciences professionals. Since 2014 we deliver outstanding industry’s expertise and support to our clients in the complete range of product life cycle : R&D, Engineering, Quality Assurance, Qualification / Validation, Regulatory Affairs, Operational Excellence, Manufacturing, Maintenance and Project Management.
Are you passionate about quality and interested in GxP environments?
Join a team where your cleaning validation skills will make a real impact on patients' lives.
- Design, plan and execute cleaning and process validation activities in accordance with regulations and guidelines
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Ensure the follow-up of the cleaning validation and the cleaning cycle development in a regulated environment
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Participate in the creation and the implementation of the cleaning validation strategy
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Execute cleaning validation tests in accordance with approved protocols, procedures and guidelines
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Write process and cleaning validation final reports that offer conclusions based on test results
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Analyze data and provide recommendations for improvements in cleaning / manufacturing process, and equipment Clean In Place (CIP)
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Provide technical leadership for deviation investigations related to cleaning validation activities (residual product/detergent and microbial contamination issues)
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Write technical cleaning evaluations as requested, including calculations, and deviations with root cause and impact assessment
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Generate the closure and validation report for cleaning validation of various equipment systems
- Degree in pharmaceutical sciences, chemical engineering, microbiology, or a related field
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Minimum 3 years of experience in cleaning validation within a GMP-regulated environment
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Strong understanding of cleaning chemistry, residue limits, analytical methods, and equipment design
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Knowledge of applicable regulatory guidance (FDA, EMA, PIC/S, ISPE, etc.)
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Experience with risk-based approaches and tools (e.g. FMEA, risk assessments)
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Excellent technical writing and communication skills
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Proficient in English and French. German is a plus
- Human-sized company with great colleagues from a large diversity of cultural and professional backgrounds
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We do care about our people, communicate openly and value feedback
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Work as a team where every member is valued and appreciated
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Opportunity to contribute to ambitious projects within an international and multicultural environment that fosters innovation, collaboration, and professional growth.
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Continuous learning and development opportunities via internal or external training and workshops
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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.
