Lonza
Head of QA Mammalian(m/w/x)
Full-timeOn-siteSenior
Visp
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TEten23 health
Head of Quality & GMP Operations(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Directing QMS development and regulatory compliance for pharmaceutical and biotech client medicine development. Proven leadership in quality system optimization and aseptic processing knowledge required. Flexible working arrangements.
Requirements
- Proven experience in a GMP-regulated environment
- Leadership in building, optimizing, or remediating Quality Management Systems (QMS)
- Strong track record managing end-to-end quality processes
- Deep understanding of aseptic processing principles
- Exceptional leadership skills
- Ability to build and foster a strong quality culture
- Strong experience working closely with manufacturing, tech ops, and supply chain teams
- Excellent communication, negotiation, and influence skills
- Strategic thinker with a pragmatic approach to problem-solving
- Strong analytical skills for data-driven decisions
Tasks
- Lead the development and optimization of Quality Management Systems (QMS)
- Ensure compliance with global GMP regulations (FDA, EMA, ICH)
- Manage core quality processes including deviations and CAPAs
- Oversee change control and document management
- Maintain comprehensive audit readiness
- Apply aseptic processing principles and contamination control strategies
- Drive cultural and operational transformation initiatives
- Foster a strong quality culture in a fast-paced environment
- Ensure accountability for quality across cross-functional teams
- Integrate compliance goals with broader business objectives
- Mentor and develop Quality Assurance professionals
- Collaborate with manufacturing, technical operations, and supply chain teams
- Engage and communicate effectively at all organizational levels
- Lead through influence and manage resistance to change
- Streamline QA processes while maintaining compliance
- Make data-driven decisions and apply risk management principles
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Flexible Working
- Flexible working arrangements
Informal Culture
- Open culture
- Diverse workforce
Career Advancement
- Career development opportunity
Learning & Development
- Wide range of training options
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.
Not a perfect match?
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Head of QA Support (Shop Floor and Batch Record Review)(m/w/x)
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Senior QMS & Compliance Expert(m/w/x)
Full-timeOn-siteSeniorVisp
TEten23 health
Head of Quality & GMP Operations(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Directing QMS development and regulatory compliance for pharmaceutical and biotech client medicine development. Proven leadership in quality system optimization and aseptic processing knowledge required. Flexible working arrangements.
Requirements
- Proven experience in a GMP-regulated environment
- Leadership in building, optimizing, or remediating Quality Management Systems (QMS)
- Strong track record managing end-to-end quality processes
- Deep understanding of aseptic processing principles
- Exceptional leadership skills
- Ability to build and foster a strong quality culture
- Strong experience working closely with manufacturing, tech ops, and supply chain teams
- Excellent communication, negotiation, and influence skills
- Strategic thinker with a pragmatic approach to problem-solving
- Strong analytical skills for data-driven decisions
Tasks
- Lead the development and optimization of Quality Management Systems (QMS)
- Ensure compliance with global GMP regulations (FDA, EMA, ICH)
- Manage core quality processes including deviations and CAPAs
- Oversee change control and document management
- Maintain comprehensive audit readiness
- Apply aseptic processing principles and contamination control strategies
- Drive cultural and operational transformation initiatives
- Foster a strong quality culture in a fast-paced environment
- Ensure accountability for quality across cross-functional teams
- Integrate compliance goals with broader business objectives
- Mentor and develop Quality Assurance professionals
- Collaborate with manufacturing, technical operations, and supply chain teams
- Engage and communicate effectively at all organizational levels
- Lead through influence and manage resistance to change
- Streamline QA processes while maintaining compliance
- Make data-driven decisions and apply risk management principles
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Flexible Working
- Flexible working arrangements
Informal Culture
- Open culture
- Diverse workforce
Career Advancement
- Career development opportunity
Learning & Development
- Wide range of training options
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
Head of QA Mammalian(m/w/x)
Full-timeOn-siteSeniorVisp - Vaxcyte
Director, Business Operations (Global Quality Control)(m/w/x)
Full-timeOn-siteManagementVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Head of QA Support (Shop Floor and Batch Record Review)(m/w/x)
Full-timeOn-siteManagementVisp - ten23 health
Senior QMS & Compliance Expert(m/w/x)
Full-timeOn-siteSeniorVisp