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.