This position serves as a subject matter expert responsible for developing global standards and best practices for high-speed automation in drug-device combination products
Job Summary
This position serves as a subject matter expert responsible for developing global standards and best practices for high-speed automation in drug-device combination products.
The role involves working closely with clients and internal stakeholders to evaluate emerging technologies and define roadmaps for equipment implementation across all PCI sites.
Candidates must possess extensive experience in structured problem solving, troubleshooting techniques, and maintaining quarterly business reviews for OEMs.
Matching Summary
This position serves as a subject matter expert responsible for developing global standards and best practices for high-speed automation in drug-device combination products.
Skills & Requirements
Must-have
7-10 years pharmaceutical assembly experience
High-speed automation equipment expertise
FAT SAT and validation knowledge
cGMP and cGCP regulatory adherence
Equipment specification and build management
Nice-to-have
Strategic technology development focus
Strong financial acumen and negotiation skills
Ability to motivate and lead teams
Experience with new product launches
Excellent presentation and communication skills
Key Requirements
Bachelor's or Master's degree in Engineering
7-10 years of pharmaceutical equipment knowledge
Advanced computer skills and professional proficiency
Ability to travel frequently
Strong analytical and decision-making capabilities