Contribute to the development of innovative pharmaceutical products by driving projects from concept to clinical execution.
This is a pivotal role that requires strategic planning, project management, and quality assurance skills. You will be responsible for managing resources, timelines, and budgets to ensure successful project delivery.
Key Responsibilities:
* Contribute to strategic planning and resource allocation across drug development programs.
* Provide timely feedback to senior leaders on project-related matters.
* Support analytical and manufacturing activities to ensure ongoing supply for clinical and development activities.
* Oversee projects in tech transfer, formulation, and method development and validation studies.
* Review and evaluate stability protocols, reports, and trend data to maintain regulatory compliance.
Requirements:
* Tertiary qualifications in Chemistry, Pharmaceutical Science, or a related discipline.
* Higher Degree qualifications in a relevant scientific field and/or MBA will be highly regarded.
* 5+ years of GMP experience in biotech or pharmaceutical settings.
* Excellent skills in project management, coordination of CDMOs, and vendor management.
* Experience managing CMC and quality activities, clinical trial supply, and analytical studies.
Benefits:
This is a rare opportunity to join an innovative team of experts and make a significant contribution to the development of exciting new drugs.
The level and title of this appointment may be higher for an experienced candidate who is an excellent fit.