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Group Specialist Pilot Plant(m/w/x)
Preparing GMP production documentation and maintaining mass balances for human plasma medicines. University student in Life Sciences or related field with fluent German/English required. Company restaurant, meal subsidy, and parking spaces.
Requirements
- University student in Life Sciences, Biotechnology, Pharmacy, Engineering, or related field
- Proficient with Microsoft 365 applications (Excel, Word)
- Fluent German and English (written and spoken)
- Open-minded, self-driven team player with collaboration skills
- First experience in GMP-regulated or pharmaceutical environment (advantageous)
Tasks
- Prepare GMP-related production documentation
- Review supplier documentation
- Enter production data in reports
- Maintain mass balances
- Update parameter sheets
- Administer GMP-relevant documentation
- Manage GMP-relevant documentation
- Support preparatory activities for pilot-scale production
- Assist in producing technical materials
- Contribute to pre-clinical material production
- Aid in clinical material production
Education
- Currently in higher education
Languages
- German – Fluent
- English – Fluent
Tools & Technologies
- Microsoft 365
- Excel
- Word
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
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Group Specialist Pilot Plant(m/w/x)
Preparing GMP production documentation and maintaining mass balances for human plasma medicines. University student in Life Sciences or related field with fluent German/English required. Company restaurant, meal subsidy, and parking spaces.
Requirements
- University student in Life Sciences, Biotechnology, Pharmacy, Engineering, or related field
- Proficient with Microsoft 365 applications (Excel, Word)
- Fluent German and English (written and spoken)
- Open-minded, self-driven team player with collaboration skills
- First experience in GMP-regulated or pharmaceutical environment (advantageous)
Tasks
- Prepare GMP-related production documentation
- Review supplier documentation
- Enter production data in reports
- Maintain mass balances
- Update parameter sheets
- Administer GMP-relevant documentation
- Manage GMP-relevant documentation
- Support preparatory activities for pilot-scale production
- Assist in producing technical materials
- Contribute to pre-clinical material production
- Aid in clinical material production
Education
- Currently in higher education
Languages
- German – Fluent
- English – Fluent
Tools & Technologies
- Microsoft 365
- Excel
- Word
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Octapharma
Industry
Pharmaceuticals
Description
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
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