REQUIREMENTS:

• Designs and undertakes high quality scientific experimentation resulting in formulation and process development of parenteral dosage forms
• Designs novel device component subassemblies for a novel device pill that support immediate and sustained release of biologics
• Assesses the chemical and physical stability of formulations in collaboration with analytical department
• Identifies appropriate stability, manufacturability, and performance issues.
• Oversees tech transfer from R&D to Manufacturing
• Interprets scientific data to derive clear conclusions and contribute to the direction for future work.
• Communicates effectively to the project team and present data at team meetings.
• Maintains high quality documentation of all activities in notebooks, reports as required.
• Keeps up to date with relevant scientific and technical developments.

EDUCATION AND JOB EXPERIENCE:

• Ph.D./M.S. in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, or related fields.
• Must have 3+ years of pharmaceutical or biotechnology research experience.
• Title will be commensurate with experience

SKILLS & SPECIFICATIONS:

• Experience in working with drug-device combination products is a plus
• Experience of working in GLP/GMP regulated environment.
• Excellent oral and written communication skills.
• The ability to work as a member of a multidisciplinary team.