Lonza
MSAT Expert Drug Product(m/w/x)
Full-timeOn-siteExperienced
Visp
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Monitoring injectable medicine material quality and risks at a pharmaceutical development and manufacturing partner. GMP environment background and ERP system experience required. Flexible working arrangements, career development opportunity.
Requirements
- Degree in scientific, technical, or pharmaceutical field
- GMP environment background (QC, QA, Supply Chain, Material Management)
- Material/supplier qualification knowledge and regulatory requirements
- Strong awareness of quality and risk
- Experienced with ERP systems (Microsoft Dynamics)
- Master data processes experience
- Proficient use of core quality tools (Deviation Management, CAPA, Change Control)
- Structured and analytical working style
- Resilience and competence to solve complex problems
- Ability to work in a dynamic environment
- Confident communication with stakeholders
- Strong team orientation
- Assertiveness
- Deep sense of responsibility
Tasks
- Assess and monitor material quality and risks
- Ensure compliance with regulatory requirements
- Maintain material data in ERP system
- Initiate actions for quality issues
- Communicate with suppliers and customers
- Define quality requirements with QC and Development
- Evaluate new materials for aseptic processes
- Resolve complex quality deviations
- Link material attributes to process performance
- Lead supplier qualification and audits
- Participate in annual supplier reviews
- Implement quality-related CAPAs
- Provide material expertise to internal and external teams
- Support material-related inquiries
- Ensure transparent and compliant documentation
- Maintain material master records
- Coordinate onboarding of new materials
- Conduct root cause analyses
- Drive CAPA processes to resolution
- Create and maintain risk-analytical documents
- Guide material updates through change control
- Initiate strategic improvement measures
- Develop material specification frameworks
- Contribute to cross-site standardization
- Enhance material quality and supplier performance
- Improve production safety
Work Experience
- 2 - 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Microsoft Dynamics
- Deviation Management
- CAPA
- Change Control
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
- Flexibility
Informal Culture
- Open culture
- Diverse workforce
- Minimal bureaucracy
Mentorship & Coaching
- Learning from experienced employees
Learning & Development
- Wide range of training options
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Other 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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Monitoring injectable medicine material quality and risks at a pharmaceutical development and manufacturing partner. GMP environment background and ERP system experience required. Flexible working arrangements, career development opportunity.
Requirements
- Degree in scientific, technical, or pharmaceutical field
- GMP environment background (QC, QA, Supply Chain, Material Management)
- Material/supplier qualification knowledge and regulatory requirements
- Strong awareness of quality and risk
- Experienced with ERP systems (Microsoft Dynamics)
- Master data processes experience
- Proficient use of core quality tools (Deviation Management, CAPA, Change Control)
- Structured and analytical working style
- Resilience and competence to solve complex problems
- Ability to work in a dynamic environment
- Confident communication with stakeholders
- Strong team orientation
- Assertiveness
- Deep sense of responsibility
Tasks
- Assess and monitor material quality and risks
- Ensure compliance with regulatory requirements
- Maintain material data in ERP system
- Initiate actions for quality issues
- Communicate with suppliers and customers
- Define quality requirements with QC and Development
- Evaluate new materials for aseptic processes
- Resolve complex quality deviations
- Link material attributes to process performance
- Lead supplier qualification and audits
- Participate in annual supplier reviews
- Implement quality-related CAPAs
- Provide material expertise to internal and external teams
- Support material-related inquiries
- Ensure transparent and compliant documentation
- Maintain material master records
- Coordinate onboarding of new materials
- Conduct root cause analyses
- Drive CAPA processes to resolution
- Create and maintain risk-analytical documents
- Guide material updates through change control
- Initiate strategic improvement measures
- Develop material specification frameworks
- Contribute to cross-site standardization
- Enhance material quality and supplier performance
- Improve production safety
Work Experience
- 2 - 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Microsoft Dynamics
- Deviation Management
- CAPA
- Change Control
Benefits
Career Advancement
- Career development opportunity
Flexible Working
- Flexible working arrangements
- Flexibility
Informal Culture
- Open culture
- Diverse workforce
- Minimal bureaucracy
Mentorship & Coaching
- Learning from experienced employees
Learning & Development
- Wide range of training options
Retirement Plans
- Competitive pension fund plan
Bonuses & Incentives
- Annual bonus
Other Benefits
- Other 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
MSAT Expert Drug Product(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
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