Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperienced
Visp
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TEten23 health
Experienced Qualification Engineer(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Leading CQV strategy for injectable medicine development and manufacturing. Master's degree or equivalent technical training with GMP plant qualification experience required. Flexible working arrangements, career development opportunity.
Requirements
- Master's/Bachelor's degree in mechanical engineering, pharmaceutical technology, medical technology, chemistry, process engineering, or similar; or technical/scientific training with suitable further training and specialisation
- Sound knowledge and several years of experience in plant qualification in GMP surrounding
- Good understanding of GMP, technical and bioprocess understanding, quality and safety awareness
- Proactive collaboration with Customer Delivery, QA, and IT Circles for seamless technical integration and culture of trust and self-responsibility
Tasks
- Lead Commissioning, Qualification, and Validation (CQV) strategy
- Plan and manage qualification projects independently
- Engage and supervise specialized external companies
- Conduct qualifications in DQ-IQ-OQ-PQ phases
- Support Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs)
- Maintain equipment in a qualified condition
- Plan and implement necessary requalifications
- Perform periodic reviews
- Develop qualification concept continuously
- Incorporate changes to standards and guidelines
- Represent department during audits and inspections
Work Experience
- 2 - 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
- Flexibility
Informal Culture
- Open culture
- Diverse workforce
- Minimal bureaucracy
Learning & Development
- Training options
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Financial and non-financial benefits
- Mutual trust
Purpose-Driven Work
- Self-responsibility
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ten23 health and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Qualifizierungsspezialist CQV(m/w/x)
Full-timeOn-siteExperiencedVisp
TEten23 health
Experienced Qualification Engineer(m/w/x)
Visp
Full-timeOn-siteExperienced
Nejo AI Summary
Leading CQV strategy for injectable medicine development and manufacturing. Master's degree or equivalent technical training with GMP plant qualification experience required. Flexible working arrangements, career development opportunity.
Requirements
- Master's/Bachelor's degree in mechanical engineering, pharmaceutical technology, medical technology, chemistry, process engineering, or similar; or technical/scientific training with suitable further training and specialisation
- Sound knowledge and several years of experience in plant qualification in GMP surrounding
- Good understanding of GMP, technical and bioprocess understanding, quality and safety awareness
- Proactive collaboration with Customer Delivery, QA, and IT Circles for seamless technical integration and culture of trust and self-responsibility
Tasks
- Lead Commissioning, Qualification, and Validation (CQV) strategy
- Plan and manage qualification projects independently
- Engage and supervise specialized external companies
- Conduct qualifications in DQ-IQ-OQ-PQ phases
- Support Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs)
- Maintain equipment in a qualified condition
- Plan and implement necessary requalifications
- Perform periodic reviews
- Develop qualification concept continuously
- Incorporate changes to standards and guidelines
- Represent department during audits and inspections
Work Experience
- 2 - 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
- Flexibility
Informal Culture
- Open culture
- Diverse workforce
- Minimal bureaucracy
Learning & Development
- Training options
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Financial and non-financial benefits
- Mutual trust
Purpose-Driven Work
- Self-responsibility
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ten23 health and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
ten23 health
Industry
Pharmaceuticals
Description
The company is a human-centric strategic partner for the pharmaceutical industry and biotech start-ups, focusing on the development and testing of medicines.
Not a perfect match?
- Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
CQV Ingenieur / Qualifizierungs- und Validierungsspezialist(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Qualifizierungsspezialist CQV(m/w/x)
Full-timeOn-siteExperiencedVisp