Lonza
Scientist QC LC-MS Biologics(m/w/x)
Full-timeOn-siteExperienced
Visp
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Leading advanced analytical activities and method development for pharmaceutical manufacturing. Extensive GMP QC experience with LC-MS and GC-MS expertise required. Relocation assistance, high-performance bonuses.
Requirements
- Master’s or PhD in chemistry, biochemistry, biotechnology, pharmacy, or related field
- Extensive experience in QC or analytical development in GMP environment
- Strong hands-on expertise in chromatography and mass spectrometry, particularly LC-MS and GC-MS
- Proven track record in analytical method development, validation, and optimization
- Solid knowledge of GMP regulations and global quality and compliance standards
- Strong technical and analytical problem-solving skills in instrumental analytics
- Demonstrated leadership abilities with capacity to guide, support, and develop team members
- Clear and confident communication skills in German and English
Tasks
- Lead advanced analytical activities
- Support quality control standards
- Take responsibility for defined QC sub-areas
- Ensure high analytical standards
- Plan and coordinate method development
- Develop LC-MS and GC-MS methods
- Validate and optimize analytical methods
- Execute routine analytical methods
- Provide technical expertise in instrumental analytics
- Act as an expert within the team
- Author and review SOPs
- Review testing procedures
- Review validation reports
- Investigate analytical issues
- Lead OOS and OOT assessments
- Train and mentor scientists
- Train laboratory colleagues
- Represent QC in cross-functional teams
- Represent QC during audits
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LC-MS
- GC-MS
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Wide range of lifestyle, family, and leisure benefits
- Access to locally tailored benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work 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.
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Leading advanced analytical activities and method development for pharmaceutical manufacturing. Extensive GMP QC experience with LC-MS and GC-MS expertise required. Relocation assistance, high-performance bonuses.
Requirements
- Master’s or PhD in chemistry, biochemistry, biotechnology, pharmacy, or related field
- Extensive experience in QC or analytical development in GMP environment
- Strong hands-on expertise in chromatography and mass spectrometry, particularly LC-MS and GC-MS
- Proven track record in analytical method development, validation, and optimization
- Solid knowledge of GMP regulations and global quality and compliance standards
- Strong technical and analytical problem-solving skills in instrumental analytics
- Demonstrated leadership abilities with capacity to guide, support, and develop team members
- Clear and confident communication skills in German and English
Tasks
- Lead advanced analytical activities
- Support quality control standards
- Take responsibility for defined QC sub-areas
- Ensure high analytical standards
- Plan and coordinate method development
- Develop LC-MS and GC-MS methods
- Validate and optimize analytical methods
- Execute routine analytical methods
- Provide technical expertise in instrumental analytics
- Act as an expert within the team
- Author and review SOPs
- Review testing procedures
- Review validation reports
- Investigate analytical issues
- Lead OOS and OOT assessments
- Train and mentor scientists
- Train laboratory colleagues
- Represent QC in cross-functional teams
- Represent QC during audits
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LC-MS
- GC-MS
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Wide range of lifestyle, family, and leisure benefits
- Access to locally tailored benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work 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?
- Lonza
Scientist QC LC-MS Biologics(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Senior Scientist QC(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
Laborant/in Quality Control(m/w/x)
Full-timeOn-siteNot specifiedVisp