CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Full-timeOn-siteSenior
Visp
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LOLonza
Manager CQV and Start-up Operations Readiness(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading senior CQV experts for biopharma facility start-up and OQ support in biologics manufacturing, establishing a local Center of Excellence. Recognized expertise in biopharma facility qualification/validation and extensive start-up experience required. Relocation assistance provided.
Requirements
- Bachelor's or Master's degree in relevant field
- Recognized expertise in biopharma facility qualification/validation
- Deep understanding of bioprocesses, GMP, biopharmaceutical manufacturing
- Extensive experience in biopharma facility start-up
- Strong leadership capabilities and team development
- Excellent communication, business acumen, team orientation
- Structured, proactive, solution-oriented working style
- Open-mindedness, receptiveness to new ideas, commitment to improvement
Tasks
- Lead and develop a team of senior CQV experts
- Manage team hiring, coaching, and performance
- Handle team compensation and disciplinary matters
- Establish and manage a local Center of Excellence
- Provide OQ support for biologics facilities
- Lead PQ for biologics facilities
- Provide operational user support during qualification and start-up
- Ensure strong operations input into commissioning activities
- Ensure strong operations input into qualification activities
- Contribute expert knowledge to capital investment projects
- Strengthen operations teams during qualification and start-up
- Drive operational start-up planning in early project phases
- Define CQV and start-up resource plans with Operations Heads
- Coordinate and facilitate start-up activities
- Manage start-up tools, procedures, and processes
- Provide start-up services to end users
- Standardize the PQ approach for GMP readiness
- Build and manage a pool of external resources
- Promote Lonza culture via collaboration and improvement
- Represent the area in the Ibex Readiness Leadership Team
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza 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.
Not a perfect match?
- Lonza
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Team Lead CSV Biologics(m/w/x)
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LOLonza
Manager CQV and Start-up Operations Readiness(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading senior CQV experts for biopharma facility start-up and OQ support in biologics manufacturing, establishing a local Center of Excellence. Recognized expertise in biopharma facility qualification/validation and extensive start-up experience required. Relocation assistance provided.
Requirements
- Bachelor's or Master's degree in relevant field
- Recognized expertise in biopharma facility qualification/validation
- Deep understanding of bioprocesses, GMP, biopharmaceutical manufacturing
- Extensive experience in biopharma facility start-up
- Strong leadership capabilities and team development
- Excellent communication, business acumen, team orientation
- Structured, proactive, solution-oriented working style
- Open-mindedness, receptiveness to new ideas, commitment to improvement
Tasks
- Lead and develop a team of senior CQV experts
- Manage team hiring, coaching, and performance
- Handle team compensation and disciplinary matters
- Establish and manage a local Center of Excellence
- Provide OQ support for biologics facilities
- Lead PQ for biologics facilities
- Provide operational user support during qualification and start-up
- Ensure strong operations input into commissioning activities
- Ensure strong operations input into qualification activities
- Contribute expert knowledge to capital investment projects
- Strengthen operations teams during qualification and start-up
- Drive operational start-up planning in early project phases
- Define CQV and start-up resource plans with Operations Heads
- Coordinate and facilitate start-up activities
- Manage start-up tools, procedures, and processes
- Provide start-up services to end users
- Standardize the PQ approach for GMP readiness
- Build and manage a pool of external resources
- Promote Lonza culture via collaboration and improvement
- Represent the area in the Ibex Readiness Leadership Team
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza 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
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Not a perfect match?
- CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Team Lead CSV Biologics(m/w/x)
Full-timeOn-siteSeniorVisp