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
Oral Solid Dose formulation
GMP readiness and audit resilience
Process monitoring and troubleshooting
Continuous improvement initiatives
Change control and documentation
Technical support for manufacturing issues
Nice-to-have
Collaboration across functions
Data-driven decision making
Stakeholder and external engagement
Inclusive and diverse team
Key Requirements
Bachelor's degree in Engineering
Minimum three (3) years related experience
Thorough knowledge of pharmaceutical/medical device industry