HIGHLY SKILLED DRUG PRODUCT PROFESSIONAL WITH STRONG PROJECT MANAGEMENT CAPABILITIES

We are seeking a highly qualified candidate with an MSc or PhD in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related field. The ideal candidate will bring extensive experience from the pharmaceutical industry, with a proven track record of leadership in drug product development and CMC project management. A solid understanding of formulation science, process development, and the clinical manufacturing of small molecules is essential.
The role requires demonstrated expertise in ing Quality by Design (QbD) frameworks, conducting risk assessments, and translating complex technical development activities into robust regulatory strategies. You should have significant experience leading cross-functional teams and collaborating effectively with external CDMOs (Contract Development and Manufacturing Organizations) and CROs (Contract Research Organizations). Strong communication, planning, and interpersonal skills are vital for success in this position, as you will work closely with both internal stakeholders and external partners to drive projects forward and ensure alignment with development goals and regulatory expectations.
Preferably, you also have experience with late-phase development and preparation for commercial manufacturing. Familiarity with lifecycle management and the development of line extension strategies is considered a strong asset. In addition, formal project management training such as PMP certificationor an equivalent qualificationis highly desirable.

Please refer the Job description for details