Experience with capa and change management processes
Fluency in german and english languages
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Lonza Group is seeking a Compliance Engineer for their sterile manufacturing site in Stein, Switzerland, focusing on ensuring GMP compliance across systems and equipment. The role involves managing documentation, audits, and inspections, requiring strong experience in the pharmaceutical industry and fluency in both German and English.
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Job Summary
This role serves as a central point of contact for GMP-related topics at the sterile manufacturing site in Stein, Switzerland.
The position involves creating and reviewing critical GMP documentation including periodic reviews, qualification documents, and SOPs.
Candidates will lead the full lifecycle of CAPAs and changes while supporting internal and external regulatory inspections.
Matching Summary
Match Score: 75
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Lonza Group is seeking a Compliance Engineer for their sterile manufacturing site in Stein, Switzerland, focusing on ensuring GMP compliance across systems and equipment. The role involves managing documentation, audits, and inspections, requiring strong experience in the pharmaceutical industry and fluency in both German and English.
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Salary
Competitive salary; Numerous lifestyle, family, and leisure benefits; Relocation assistance available
Skills & Requirements
Must-have
Strong GMP knowledge in pharmaceutical industry
Experience with CAPA and change management processes
Fluency in German and English languages
Nice-to-have
Agile career development opportunities
Collaborative inclusive work culture
Structured detail-oriented working style
Key Requirements
Bachelor's degree in Pharmacy, Engineering, or related technical field
Strong experience in pharmaceutical industry with GMP focus