This is an exciting opportunity to work in a collaborative, science-driven environment where you'll have ownership of projects, solve complex technical challenges, and contribute to delivering high-quality medicines that make a difference to patients worldwide.
What You'll Do
As part of our team, you will:
- Design, plan, and execute laboratory studies to support formulation development, process optimization, scale-up activities, and technology transfers.
- Perform and support parenteral drug product activities including compounding, filtration, and filling operations.
- Analyze and interpret scientific data, identify trends, troubleshoot issues, and make data-driven recommendations.
- Author and review technical documents, protocols, reports, procedures, and batch records.
- Support laboratory start-up activities, equipment qualification, and facility readiness in collaboration with engineering, quality, and manufacturing teams.
- Work with internal stakeholders and external vendors to evaluate and improve equipment, systems, and technologies.
- Lead or contribute to investigations, risk assessments, change controls, and problem-solving initiatives.
- Ensure compliance with GMP, quality, data integrity, and safety requirements.
- Drive continuous improvement, digitalization, and knowledge-sharing initiatives across the team.