Lonza
Group Leader Analytical Development (Small Molecules)(m/w/x)
Full-timeOn-siteSenior
Visp
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LOLonza
Senior MSAT Specialist, Small Molecules(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading impurity risk assessments for small molecule API manufacturing. Strong GMP experience and data interpretation skills required. Relocation assistance, agile career path.
Requirements
- University degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or comparable discipline
- Solid experience in GMP-regulated environment, ideally Small Molecule API, pharmaceutical manufacturing, MSAT, Process Development, QA, or QC
- Strong ability to interpret process and analytical data
- Excellent technical writing skills, clear and concise documentation
- Confident communicator, ability to align stakeholders
- High level of collaboration, autonomy, accountability, pragmatic mindset
- Fluency in English
- German language skills considered an advantage
Tasks
- Lead impurity risk assessments
- Shape control strategies for impurity compliance
- Evaluate manufacturing processes for impurity risks
- Document risk-based testing concepts
- Set acceptance criteria and sampling approaches
- Conduct periodic reviews of impurity controls
- Support technology transfers and investigations
- Manage deviations and change controls
- Identify compliance gaps and product impacts
- Provide pragmatic mitigation plans
- Ensure audit-ready documentation
- Collaborate with cross-functional teams
- Work with QC, QA, Manufacturing, and Procurement
- Engage with EHS and external partners
- Maintain sustainable compliance standards
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
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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LOLonza
Senior MSAT Specialist, Small Molecules(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Leading impurity risk assessments for small molecule API manufacturing. Strong GMP experience and data interpretation skills required. Relocation assistance, agile career path.
Requirements
- University degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or comparable discipline
- Solid experience in GMP-regulated environment, ideally Small Molecule API, pharmaceutical manufacturing, MSAT, Process Development, QA, or QC
- Strong ability to interpret process and analytical data
- Excellent technical writing skills, clear and concise documentation
- Confident communicator, ability to align stakeholders
- High level of collaboration, autonomy, accountability, pragmatic mindset
- Fluency in English
- German language skills considered an advantage
Tasks
- Lead impurity risk assessments
- Shape control strategies for impurity compliance
- Evaluate manufacturing processes for impurity risks
- Document risk-based testing concepts
- Set acceptance criteria and sampling approaches
- Conduct periodic reviews of impurity controls
- Support technology transfers and investigations
- Manage deviations and change controls
- Identify compliance gaps and product impacts
- Provide pragmatic mitigation plans
- Ensure audit-ready documentation
- Collaborate with cross-functional teams
- Work with QC, QA, Manufacturing, and Procurement
- Engage with EHS and external partners
- Maintain sustainable compliance standards
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Fluent
- German – Basic
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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
Group Leader Analytical Development (Small Molecules)(m/w/x)
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Full-timeOn-siteSeniorVisp - Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
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Senior QA Automation Specialist(m/w/x)
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