About the Role
Responsibilities:
Consult with global manufacturing sites to define equipment and process requirements (, URS), complete technical design reviews, and support fit-for-purpose solutions across oral solid dose and sterile operations.
Conduct structured troubleshooting and root-cause investigations for process and equipment performance issues; recommend and support implementation of sustainable corrective and preventive actions.
Provide technical input for major capital projects from concept through detailed design, ensuring alignment with cGMP expectations and business objectives.
Partner with Plant Engineering, Technical Services/Manufacturing Sciences (TS/MS), Quality, and R&D to support technology transfer, product launches, and validation strategy through robust technical risk assessment and problem solving.
Develop and standardize best practices, tools, and training to strengthen engineering capab...
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