CH12 Lonza AG
Intern in QC Biologics(m/w/x)
Full-timeInternshipOn-site
Visp
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Supporting GMP compliance and documentation for injectable medicines. Previous lab or GMP experience highly desirable. Paid learning opportunity with flexible start date.
Requirements
- Previous research laboratory experience (highly desirable)
- Prior Good Manufacturing Practices (GMP) experience (highly desirable)
- Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Biotechnology, Biochemistry, Biology, or related field
- Willingness to work on-site in Visp
- Fluency in written and spoken English
- Growth mindset, creative thinking, independent problem-solving
- Strong organizational and interpersonal skills, collaborative approach
Tasks
- Support QA activities in production and documentation
- Ensure compliance with GMP and regulatory standards
- Collaborate with QC, Production, and R&D teams
- Drive continuous improvement efforts
Education
- Currently in higher educationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Learning & Development
- Paid learning opportunity
- Gain expertise
- Develop professional skills
Flexible Working
- Flexible start date
Career Advancement
- Boost placement prospects
- Potential placement opportunities
Mentorship & Coaching
- Work alongside experienced researchers
Other Benefits
- Hands-on research experience
Purpose-Driven Work
- Contribute to innovative solutions
Informal Culture
- Supportive and collaborative environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ten23 health 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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Supporting GMP compliance and documentation for injectable medicines. Previous lab or GMP experience highly desirable. Paid learning opportunity with flexible start date.
Requirements
- Previous research laboratory experience (highly desirable)
- Prior Good Manufacturing Practices (GMP) experience (highly desirable)
- Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Biotechnology, Biochemistry, Biology, or related field
- Willingness to work on-site in Visp
- Fluency in written and spoken English
- Growth mindset, creative thinking, independent problem-solving
- Strong organizational and interpersonal skills, collaborative approach
Tasks
- Support QA activities in production and documentation
- Ensure compliance with GMP and regulatory standards
- Collaborate with QC, Production, and R&D teams
- Drive continuous improvement efforts
Education
- Currently in higher educationOR
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Learning & Development
- Paid learning opportunity
- Gain expertise
- Develop professional skills
Flexible Working
- Flexible start date
Career Advancement
- Boost placement prospects
- Potential placement opportunities
Mentorship & Coaching
- Work alongside experienced researchers
Other Benefits
- Hands-on research experience
Purpose-Driven Work
- Contribute to innovative solutions
Informal Culture
- Supportive and collaborative environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ten23 health 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
ten23 health
Industry
Pharmaceuticals
Description
The company is a human-centric strategic partner for the pharmaceutical industry and biotech start-ups, focusing on the development and testing of medicines.
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