Lead the planning, execution, and coordination of sterile product development in the formulation lab, focusing on parenteral small molecule and peptide dosage forms.

Design, review, and recommend changes to scientific protocols and procedures for aseptic processing and sterile manufacturing.

Perform data analysis, present results, and troubleshoot issues related to parenteral formulation stability, sterility, and manufacturing processes.

Author scientific reports, SOPs, and support the preparation of registration documents.

Oversee and provide technical guidance to external partners, ensuring adherence to cGMP for sterile products.

PhD degree in Pharmaceutical Science

A minimum of 5 years of experience in the pharmaceutical industry

Min. 3 years of demonstrated expertise in f...