Lonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Full-timeOn-siteSenior
Visp
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CHCH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading and developing a local expert team for biopharma production facilities at a global life sciences firm. Extensive experience with validation processes for biopharma production environments and GMP understanding required. Full HR responsibility for team development and compensation decisions.
Requirements
- Bachelor, Master, Diploma in technical field or equivalent experience
- Extensive experience in commissioning, qualification and validation (CQV) in biotech environment
- Depth understanding of bioprocesses, GMP and biopharma production
- Strong experience in CQV project management
- Strong leadership skills and ability to communicate at higher levels
- Strong business understanding in a CDMO environment
- Fluency in English, German language skills advantageous
Tasks
- Lead a team of senior CQV experts
- Manage human resource functions including qualification and development
- Mentor and hire team members
- Make pay decisions and address team issues
- Establish and manage a local group of CQV experts for biologics facilities
- Support future operations users during periodic qualification
- Collaborate on capital investment projects
- Enhance operations teams with CQV expertise
- Plan CQV activities to ensure resource availability for projects
- Facilitate collaboration among key stakeholders
- Secure operations input for CQ as a gatekeeper
- Define and standardize the PQ approach
- Build and manage a pool of external resources for CQV operations
- Promote a culture of openness and teamwork
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – is a plus
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic working culture
Informal Culture
- Inclusive workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG 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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CQV Engineer / Qualification & Validation Engineer(m/w/x)
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CHCH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading and developing a local expert team for biopharma production facilities at a global life sciences firm. Extensive experience with validation processes for biopharma production environments and GMP understanding required. Full HR responsibility for team development and compensation decisions.
Requirements
- Bachelor, Master, Diploma in technical field or equivalent experience
- Extensive experience in commissioning, qualification and validation (CQV) in biotech environment
- Depth understanding of bioprocesses, GMP and biopharma production
- Strong experience in CQV project management
- Strong leadership skills and ability to communicate at higher levels
- Strong business understanding in a CDMO environment
- Fluency in English, German language skills advantageous
Tasks
- Lead a team of senior CQV experts
- Manage human resource functions including qualification and development
- Mentor and hire team members
- Make pay decisions and address team issues
- Establish and manage a local group of CQV experts for biologics facilities
- Support future operations users during periodic qualification
- Collaborate on capital investment projects
- Enhance operations teams with CQV expertise
- Plan CQV activities to ensure resource availability for projects
- Facilitate collaboration among key stakeholders
- Secure operations input for CQ as a gatekeeper
- Define and standardize the PQ approach
- Build and manage a pool of external resources for CQV operations
- Promote a culture of openness and teamwork
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – is a plus
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Numerous lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic working culture
Informal Culture
- Inclusive workplace
Other Benefits
- Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of CH12 Lonza AG 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
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Not a perfect match?
- Lonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Team Lead CSV Biologics(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Associate Director Operation Readiness Lead(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp