The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.
Join Lonza Pharma & Biotech and help bring life-changing therapies to patients around the world. As an Experienced MSAT Engineer, you will be at the forefront of technical operations, partnering with cross-functional teams to optimize manufacturing processes, lead continuous improvement initiatives, and solve complex scientific and engineering challenges. This is an exciting opportunity to make a measurable impact while advancing your career within a global leader in life sciences.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
- Medical, dental, and vision insurance.
- Opportunities to lead technical initiatives and influence manufacturing excellence.
- Exposure to innovative pharmaceutical manufacturing technologies and cross-functional collaboration.
- The opportunity to help deliver life-changing therapies to patients around the world.
What you will do - Serve as the primary process owner for commercial products, ensuring safe, compliant, and reliable manufacturing operations.
- Lead technology transfer activities and support commercial manufacturing campaigns for pharmaceutical products.
- Partner with customers, project teams, and manufacturing stakeholders to solve technical challenges and improve process performance.
- Drive operational excellence by identifying and implementing improvements that enhance yield, efficiency, quality, and cost performance.
- Lead investigations, root cause analyses, risk assessments, and corrective action activities using data-driven methodologies.
- Support regulatory inspections, process validation, commissioning, qualification, and ongoing process verification activities.
- Mentor colleagues, support operator training, and contribute to technical expertise development across the site.
What we are looking for - Bachelor's degree in Engineering, Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Experience within pharmaceutical manufacturing or a related regulated industry.
- Strong understanding of current Good Manufacturing Practice (cGMP) requirements and manufacturing processes.
- Experience using scientific and engineering principles to solve complex technical challenges.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent communication and stakeholder management skills, with the ability to collaborate across teams.
- Commitment to quality, safety, continuous improvement, and consistent on-site attendance.
Ready to shape the future of life sciences? Apply now.
