Key Responsibilities
This role will play a crucial part in driving strategy harmonization and leading drug product process development.
* Develop, optimize, and validate robust processes for clinical and commercial parenteral drug products.
* Lead process design, validation studies, and technical transfers for seamless commercialization.
* Cross-functionally collaborate and ensure strategic alignment and successful project execution.
* Foster innovation and continuous improvement in drug product and equipment processes.
* Ensure compliance with regulatory standards.
Requirements
To succeed in this position, you will need:
* Ph.D. in a related scientific or engineering field or equivalent experience.
* 10+ years of biopharmaceutical industry experience and proven leadership skills.
* Experience with implementing advanced Process Analytical Technologies and/or drug device combination product processes is advantageous.
* Expertise in parenteral process development and regulatory submissions.
* Strong leadership and project management capabilities.
* Excellent communication, strategic thinking, and problem-solving skills.
About This Opportunity
An Equal Opportunity Employer committed to advancing science and ensuring everyone has access to healthcare today and for generations to come.