About the Role

Responsibilities:

  • 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.

  • What You Need to Succeed (minimum qualifications):

  • PhD degree in Pharmaceutical Science

  • A minimum of 5 years of experience in the pharmaceutical industry

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