Fresenius Kabi SwissBioSim GmbH
Regulatory Affairs Specialist Intern(m/w/x)
Full-timeInternshipOn-site
Eysins
from CHF 60,000 / year
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SUSUSONITY
Internship - Compliance Biotech(m/w/x)
Aubonne
Full-timeInternshipOn-site
Nejo AI Summary
Ensuring cGMP production compliance for protein manufacturing. Basic GMP and pharmaceutical environment knowledge required. Continuous improvement project participation, update work instructions and batch records.
Requirements
- Engineering degree in biotechnology, life sciences, health, or equivalent
- Studies related to Compliance or Quality Assurance
- Basic knowledge of GMP standards and active ingredient production regulations
- Basic knowledge of pharmaceutical environment behavior
- Knowledge of biotechnological principles for protein manufacturing in pharmaceutical production
- Proficiency in office software
Tasks
- Ensure production compliance with cGMP standards
- Implement CAPAs and Change Controls to maintain compliance
- Resolve deviations and maintain compliance within deadlines
- Participate in continuous improvement projects
- Update work instructions and batch records
- Develop and implement risk mitigation actions
- Maintain and review procedures and necessary documents
- Ensure GMP status of activities in your domain
- Collaborate with the team to ensure data traceability and integrity
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Office software
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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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SUSUSONITY
Internship - Compliance Biotech(m/w/x)
Aubonne
Full-timeInternshipOn-site
Nejo AI Summary
Ensuring cGMP production compliance for protein manufacturing. Basic GMP and pharmaceutical environment knowledge required. Continuous improvement project participation, update work instructions and batch records.
Requirements
- Engineering degree in biotechnology, life sciences, health, or equivalent
- Studies related to Compliance or Quality Assurance
- Basic knowledge of GMP standards and active ingredient production regulations
- Basic knowledge of pharmaceutical environment behavior
- Knowledge of biotechnological principles for protein manufacturing in pharmaceutical production
- Proficiency in office software
Tasks
- Ensure production compliance with cGMP standards
- Implement CAPAs and Change Controls to maintain compliance
- Resolve deviations and maintain compliance within deadlines
- Participate in continuous improvement projects
- Update work instructions and batch records
- Develop and implement risk mitigation actions
- Maintain and review procedures and necessary documents
- Ensure GMP status of activities in your domain
- Collaborate with the team to ensure data traceability and integrity
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- Office software
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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
SUSONITY
Industry
Healthcare
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
Not a perfect match?
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