Offer summary
Qualifications:
Strong understanding of contemporary formulation science, Experience in lyophilized parenteral products development, Working knowledge of synthetic peptides and PEGylated materials, Sterile drug product manufacturing experience, Excellent grasp of related disciplines like regulatory standards.
Key responsabilities:
- Design, develop and validate formulated products
- Improve productivity and efficiency in projects
- Collaborate with diverse CDMO teams
- Ensure data integrity and compliance with regulatory standards
- Develop scientifically sound formulations and products