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QC Raw Material Specialist(m/w/x)
Description
In this Visp-based role, you will drive the quality and compliance of raw materials by leading cross-functional projects and coordinating complex approval workflows across the laboratories.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •PhD or equivalent Life Sciences experience
- •Advantageous pharmaceutical, biotechnological GMP, or QC experience
- •Proficient use of MS Office
- •Advantageous pharmaceutical or laboratory software knowledge
- •Enjoyment of cross-functional collaboration
- •Organizational and project management skills
- •Integrity and assertiveness in communication
- •Excellent English communication skills
- •Advantageous German communication skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Lead QC projects in cross-functional teams
- •Collaborate with labs, program management, and production
- •Coordinate material onboarding with procurement and supply chain
- •Manage material evaluation and approval workflows
- •Track testing and documentation for material qualification
- •Facilitate laboratory analyses and project approvals
- •Prepare reports to improve product quality
- •Plan and supervise experimental laboratory work
- •Develop specifications and handling instructions for materials
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •High performance compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Other Benefits
- •Relocation assistance
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QC Raw Material Specialist(m/w/x)
The AI Job Search Engine
Description
In this Visp-based role, you will drive the quality and compliance of raw materials by leading cross-functional projects and coordinating complex approval workflows across the laboratories.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •PhD or equivalent Life Sciences experience
- •Advantageous pharmaceutical, biotechnological GMP, or QC experience
- •Proficient use of MS Office
- •Advantageous pharmaceutical or laboratory software knowledge
- •Enjoyment of cross-functional collaboration
- •Organizational and project management skills
- •Integrity and assertiveness in communication
- •Excellent English communication skills
- •Advantageous German communication skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Lead QC projects in cross-functional teams
- •Collaborate with labs, program management, and production
- •Coordinate material onboarding with procurement and supply chain
- •Manage material evaluation and approval workflows
- •Track testing and documentation for material qualification
- •Facilitate laboratory analyses and project approvals
- •Prepare reports to improve product quality
- •Plan and supervise experimental laboratory work
- •Develop specifications and handling instructions for materials
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •High performance compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Other Benefits
- •Relocation assistance
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.
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