CH12 Lonza AG
Scientist Process Development(m/w/x)
Full-timeOn-siteJunior
Basel, Stein (AR)
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LOLonza
Senior Scientist Process Development Drug Product(m/w/x)
Basel, Stein (AR)
Full-timeOn-siteSenior
Nejo AI Summary
Establishing drug product process development infrastructure and qualifying equipment for non-GMP manufacturing. Minimum 3 years pharmaceutical industry experience required. Agile career path, dynamic work culture.
Requirements
- BSc or MSc in Pharmaceutical Sciences, Chemical or Biochemical Engineering
- Minimum 3 years experience in pharmaceutical or chemical industry
- Working experience in pharmaceutical development and manufacturing technologies
- Very good knowledge of reporting, interpretation, and documentation of scientific results
- Experience with parenteral dosage forms and/or lyophilization techniques (plus)
- Ability to work independently in a team environment
- Attention to detail
- Proactive attitude
- Good knowledge of written and spoken English
- Experience with parenteral dosage forms, protein formulation and analytics, and aseptic working techniques (plus)
Tasks
- Assist in establishing Drug Product process development infrastructure
- Install and qualify equipment for process development and non-GMP manufacturing
- Maintain equipment in alignment with best practices and regulations
- Plan and perform process development and characterization studies
- Develop processes for liquid and lyophilized parenteral drug products
- Supervise junior scientists and interns as needed
- Document data following lab procedures and documentation practices
- Understand and apply Annex1 regulations to GMP Drug Product manufacturing
- Support non-clinical and clinical drug supply manufacturing at GMP sites
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
Bonuses & Incentives
- Performance-based compensation
Other Benefits
- Full time
- 80-100% employment
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 Scientist Process Development Drug Product(m/w/x)
Basel, Stein (AR)
Full-timeOn-siteSenior
Nejo AI Summary
Establishing drug product process development infrastructure and qualifying equipment for non-GMP manufacturing. Minimum 3 years pharmaceutical industry experience required. Agile career path, dynamic work culture.
Requirements
- BSc or MSc in Pharmaceutical Sciences, Chemical or Biochemical Engineering
- Minimum 3 years experience in pharmaceutical or chemical industry
- Working experience in pharmaceutical development and manufacturing technologies
- Very good knowledge of reporting, interpretation, and documentation of scientific results
- Experience with parenteral dosage forms and/or lyophilization techniques (plus)
- Ability to work independently in a team environment
- Attention to detail
- Proactive attitude
- Good knowledge of written and spoken English
- Experience with parenteral dosage forms, protein formulation and analytics, and aseptic working techniques (plus)
Tasks
- Assist in establishing Drug Product process development infrastructure
- Install and qualify equipment for process development and non-GMP manufacturing
- Maintain equipment in alignment with best practices and regulations
- Plan and perform process development and characterization studies
- Develop processes for liquid and lyophilized parenteral drug products
- Supervise junior scientists and interns as needed
- Document data following lab procedures and documentation practices
- Understand and apply Annex1 regulations to GMP Drug Product manufacturing
- Support non-clinical and clinical drug supply manufacturing at GMP sites
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
- Inclusive workplace
Purpose-Driven Work
- Ethical workplace
Bonuses & Incentives
- Performance-based compensation
Other Benefits
- Full time
- 80-100% employment
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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Full-timeOn-siteSeniorBasel - CH12 Lonza AG
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Full-timeOn-siteSeniorBasel, Stein (AR)