CH12 Lonza AG
Project Leader Biopharmaceutical Quality Control(m/w/x)
Full-timeOn-siteExperienced
Visp
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Representing QC in project teams at global life sciences company, communicating with manufacturing and customers. Proficient MS Office use required. Relocation assistance provided.
Requirements
- PhD or equivalent Life Sciences experience
- GMP environment and Quality Control experience (plus)
- Proficient MS Office use required
- Pharmaceutical/laboratory software knowledge (plus)
- Enjoyment of working with diverse business areas
- Organizational and project management skills
- Communication with integrity and assertiveness
- Excellent English communication skills (must)
- German communication skills (advantage)
Tasks
- Communicate with manufacturing, QA, and customers
- Represent QC in project teams
- Make independent decisions
- Collaborate with labs, program management, production, and quality assurance
- Establish and maintain customer relationships
- Prepare and support production campaigns
- Process change requests and deviations under GMP
- Support customer audits and inspections by authorities
- Calculate and monitor QC costs in the project
- Coordinate, prioritize, and schedule tasks independently
Work Experience
- approx. 1 - 4 years
Education
- Doctoral / PhD
Languages
- English – Native
- German – Basic
Tools & Technologies
- MS Office
- Documentum
- LIMS
- Trackwise
Benefits
Other Benefits
- Relocation assistance
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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Representing QC in project teams at global life sciences company, communicating with manufacturing and customers. Proficient MS Office use required. Relocation assistance provided.
Requirements
- PhD or equivalent Life Sciences experience
- GMP environment and Quality Control experience (plus)
- Proficient MS Office use required
- Pharmaceutical/laboratory software knowledge (plus)
- Enjoyment of working with diverse business areas
- Organizational and project management skills
- Communication with integrity and assertiveness
- Excellent English communication skills (must)
- German communication skills (advantage)
Tasks
- Communicate with manufacturing, QA, and customers
- Represent QC in project teams
- Make independent decisions
- Collaborate with labs, program management, production, and quality assurance
- Establish and maintain customer relationships
- Prepare and support production campaigns
- Process change requests and deviations under GMP
- Support customer audits and inspections by authorities
- Calculate and monitor QC costs in the project
- Coordinate, prioritize, and schedule tasks independently
Work Experience
- approx. 1 - 4 years
Education
- Doctoral / PhD
Languages
- English – Native
- German – Basic
Tools & Technologies
- MS Office
- Documentum
- LIMS
- Trackwise
Benefits
Other Benefits
- Relocation assistance
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?
- CH12 Lonza AG
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