MSAT Engineer

Join us where innovation meets impact. In this role, you will support GMP manufacturing operations for oral solid dose products, ensuring processes run efficiently, safely, and with the highest quality standards. You’ll play a key part in advancing pharmaceutical programs that help bring life-changing medicines to patients worldwide.

A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus.
• Medical, dental and vision insurance.
• 401(k) matching plan.
• Life insurance, as well as short-term and long-term disability insurance.
• Employee assistance programs.
• Paid time off (PTO).

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

Provide technical support for GMP oral solid dose manufacturing processes, including blending, granulation, encapsulation, tableting, and coating operations.

Plan, coordinate, and track project timelines and deliverables to ensure successful on‑time execution.

Apply chemical engineering and materials science principles to develop, optimize, and troubleshoot manufacturing processes.

Prepare technical documentation such as master batch records, protocols, and engineering study reports.

Lead process and technical investigations, performing root cause analysis, product impact assessments, and supporting effective CAPA development.

Analyze complex data sets using statistical tools (e.g., SPC, ANOVA, regression, multivariate analysis) to drive continuous improvement.

Collaborate cross‑functionally with internal teams and clients to enhance processes, improve efficiency, and support ongoing production needs.

Bachelor’s degree required, preferably in a Science or Engineering discipline.

Experience in pharmaceutical manufacturing, with familiarity in cGMP environments strongly preferred.

Understanding of OSD unit operations such as blending, granulation, encapsulation, tableting, and coating preferred.

Ability to apply engineering and scientific fundamentals to solve technical problems.

Proficiency in data analysis and interpretation using statistical methods and approved systems.

Strong commitment to safety, regulatory compliance, and collaborative teamwork.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.