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수평: Entry level
직업 종류: Full-time
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작업 내용
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there is no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be a part of.We are looking for a QA Specialist CSV and Data Integrity for our Visp location.Key Responsibilities- Ensure compliance with regulatory and company requirements and quality standards for the validation of computerized systems at the Visp site
- Ensure that internal policies comply with regulatory guidelines
- Coordinate validation activities of computerized systems with other departments
- Ensure proper application of change control procedures in validation activities
- Ensure and maintain validation status of computerized systems
- Participate in audits and inspections
- Review and approve deviation reports, change requests and CAPAs in the CSV environment
- Participate in risk assessment in the CSV environment
- Creation, review and management of SOPs
- Bachelor’s degree in biotechnology, chemistry or related field or equivalent apprenticeship
- Experience in the pharmaceutical industry, preferably in the quality area
- Experience in a GMP regulated environment in the pharmaceutical industry
- Verbal and written skills in German and English
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마감 시간: 09-06-2024
무료 후보 신청 클릭
작업 보고
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