Qualifications

• Master's degree in Pharmaceutical Sciences, Formulation Chemistry, or closely related field required.
• 5 years of experience in pharmaceutical formulation development, process development, and technology transfer activities.
• 2 years of experience with FDA and ICH product development regulatory requirements.
• 2 years of experience in Quality by Design (QbD) principles, including DoE and risk assessment.
• 2 years of experience in data analysis for formulation and process development.

Responsibilities

• Conduct pharmaceutical formulation and process development activities.
• Implement technology transfer for scale-up to production.
• Ensure compliance with FDA and ICH regulatory guidelines for product development.
• Apply Quality by Design methodologies to enhance development processes.
• Analyze and interpret data to inform formulation and process decisions.

Benefits

• Collaborative work environment focused on innovation.
• Opportunity to influence cutting-edge pharmaceutical developments.
• Professional development opportunities in regulatory affairs and formulation science.
• Access to advanced research facilities.