Lonza
Senior GMP Validation Scientist – Validation Strategy & Documentation Physico-Chemical Quality Control(m/w/x)
Full-timeOn-siteSenior
Basel
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Leading a GMP Services team, overseeing task planning and employee development for medicine manufacturing at a global life sciences firm. MSc in Pharmaceutical Sciences or related field, 5-10 years analytical chemistry in GMP, and 3+ years team leadership experience required. Agile career.
Requirements
- MSc in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field; PhD preferred
- 5-10 years experience in analytical chemistry in GMP settings
- 5-10 years experience in audits and inspections, acting as SME
- 3+ years experience in team leadership and people management
- Strong technical writing skills for quality documentation
- Clear communication and collaborative work ability
- Experience with document management and quality process systems (plus)
- Fluency in English; German (plus)
Tasks
- Lead and support the GMP Services team
- Plan and prioritize team tasks
- Onboard new employees
- Guide employee performance and development
- Ensure efficient use of time and personnel
- Represent Lonza in audits and inspections
- Provide lab tours during audits
- Offer expert insights during inspections
- Manage complex quality records
- Handle deviations
- Process change requests
- Oversee investigations
Work Experience
- 5 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Competitive Pay
- High-performance compensation programs
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.
Not a perfect match?
- Roche
Group Head in Analytical Development & Quality Control(m/w/x)
Full-timeOn-siteManagementBasel - Roche
Head of QA for QC(m/w/x)
Full-timeOn-siteSeniorKaiseraugst - Lonza
Director, Site Quality Head Drug Product(m/w/x)
Full-timeOn-siteManagementBasel - Lonza
Project Scientist Team Manager, Physico-Chemical Quality Control(m/w/x)
Full-timeOn-siteManagementBasel
Leading a GMP Services team, overseeing task planning and employee development for medicine manufacturing at a global life sciences firm. MSc in Pharmaceutical Sciences or related field, 5-10 years analytical chemistry in GMP, and 3+ years team leadership experience required. Agile career.
Requirements
- MSc in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field; PhD preferred
- 5-10 years experience in analytical chemistry in GMP settings
- 5-10 years experience in audits and inspections, acting as SME
- 3+ years experience in team leadership and people management
- Strong technical writing skills for quality documentation
- Clear communication and collaborative work ability
- Experience with document management and quality process systems (plus)
- Fluency in English; German (plus)
Tasks
- Lead and support the GMP Services team
- Plan and prioritize team tasks
- Onboard new employees
- Guide employee performance and development
- Ensure efficient use of time and personnel
- Represent Lonza in audits and inspections
- Provide lab tours during audits
- Offer expert insights during inspections
- Manage complex quality records
- Handle deviations
- Process change requests
- Oversee investigations
Work Experience
- 5 - 10 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Benefits
Career Advancement
- Agile career
Startup Environment
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Competitive Pay
- High-performance compensation programs
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
Senior GMP Validation Scientist – Validation Strategy & Documentation Physico-Chemical Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel - Roche
Group Head in Analytical Development & Quality Control(m/w/x)
Full-timeOn-siteManagementBasel - Roche
Head of QA for QC(m/w/x)
Full-timeOn-siteSeniorKaiseraugst - Lonza
Director, Site Quality Head Drug Product(m/w/x)
Full-timeOn-siteManagementBasel - Lonza
Project Scientist Team Manager, Physico-Chemical Quality Control(m/w/x)
Full-timeOn-siteManagementBasel