Key Responsibilities:
- Design and execute pre-formulation studies, prototype batches, and scale-up trials.
- Collaborate with cross-functional teams for tech transfer, stability studies, and regulatory documentation.
- Ensure compliance with cGMP, ICH guidelines, and global regulatory standards.
- Mentor junior scientists and manage lab operations efficiently.
Qualifications & Skills:
- 715 years of hands-on experience in formulation development.
- Strong knowledge of QbD, DoE, and analytical techniques.
- Experience with USFDA, EMA, or ROW submissions preferred.
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