Provide technical process engineering support for oral solid dose (OSD) formulation operations to ensure safe, compliant, and efficient manufacturing
Job Summary
Provide technical process engineering support for oral solid dose (OSD) formulation operations to ensure safe, compliant, and efficient manufacturing.
Contribute to GMP readiness and audit resilience by maintaining strong documentation, deviation/CAPA effectiveness, and data integrity.
IPR provides a comprehensive benefits package for its employees. It includes: Health, Pharmacy, Dental and Vision Insurances, STD and LTD Insurances, Retirement Plan with company match and Profit Sharing among others.
Matching Summary
Provide technical process engineering support for oral solid dose (OSD) formulation operations to ensure safe, compliant, and efficient manufacturing.
Skills & Requirements
Must-have
OSD formulation operations
process monitoring and troubleshooting
GMP readiness and audit resilience
supply continuity
cGMP compliance
technical process engineering support
Nice-to-have
digital batch records/EBR improvements
PAT deployment
disciplined problem-solving
data-driven decision making
Key Requirements
Bachelor's degree in Engineering
minimum of three (3) years related experience
pharmaceutical/medical device industry manufacturing knowledge
project management experience
change control principles knowledge
financial analyses utilization
automation and equipment programs/control basic knowledge