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Formulation Project Manager(m/w/x)
Managing IMP manufacturing for complex oral solids, including formulation development and tech transfers. Pharmaceutical technology and GMP experience required. Collaboration with QA/QC and Production, guiding lab operators.
Requirements
- Degree in pharmacy or technology
- In-depth knowledge of pharmaceutical technology, process requirements, and product development, Tech Transfers / MS&T
- Experience with solid dosage forms in GMP regulated environment (advantageous)
- Knowledge of pharmaceutical excipients, regulations, and pharmacopoeia monographs (European/United States/Japanese)
- Deep understanding of ICH guidelines, AMWHV, EU-GMP, EMA, and FDA guidelines
- Solution-oriented and analytical thinking
- Good coordination and organizational skills
- Entrepreneurial thinking, flexibility, and innovative spirit
- Systematic, structured, conscientious, and open to new ideas
- Excellent communication skills in German (native) and English
- Strong teamwork ability
- High customer centricity
Tasks
- Supervise, organize, and coordinate preclinical and clinical IMP manufacturing
- Manage pharmaceutical transfer projects for oral solids
- Develop formulations and manufacturing processes for new drugs
- Collaborate with other departments on development activities
- Guide Lab Operators and align with Project Management, QA/QC, and Production
- Create manufacturing documents and sampling instructions
- Implement in-process controls according to SOPs and guidelines
- Monitor experiments and interpret data scientifically
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
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Formulation Project Manager(m/w/x)
Managing IMP manufacturing for complex oral solids, including formulation development and tech transfers. Pharmaceutical technology and GMP experience required. Collaboration with QA/QC and Production, guiding lab operators.
Requirements
- Degree in pharmacy or technology
- In-depth knowledge of pharmaceutical technology, process requirements, and product development, Tech Transfers / MS&T
- Experience with solid dosage forms in GMP regulated environment (advantageous)
- Knowledge of pharmaceutical excipients, regulations, and pharmacopoeia monographs (European/United States/Japanese)
- Deep understanding of ICH guidelines, AMWHV, EU-GMP, EMA, and FDA guidelines
- Solution-oriented and analytical thinking
- Good coordination and organizational skills
- Entrepreneurial thinking, flexibility, and innovative spirit
- Systematic, structured, conscientious, and open to new ideas
- Excellent communication skills in German (native) and English
- Strong teamwork ability
- High customer centricity
Tasks
- Supervise, organize, and coordinate preclinical and clinical IMP manufacturing
- Manage pharmaceutical transfer projects for oral solids
- Develop formulations and manufacturing processes for new drugs
- Collaborate with other departments on development activities
- Guide Lab Operators and align with Project Management, QA/QC, and Production
- Create manufacturing documents and sampling instructions
- Implement in-process controls according to SOPs and guidelines
- Monitor experiments and interpret data scientifically
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
SwissCo Services AG
Industry
Pharmaceuticals
Description
Das Unternehmen ist einer der weltweit führenden Auftragshersteller und -entwickler für die Pharmaindustrie.
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