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, including Health, Pharmacy, Dental and Vision Insurances, STD and LTD Insurances, Retirement Plan with company match and Profit Sharing.
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
Technical support for manufacturing issues
Change control and documentation
Nice-to-have
Data-driven decision making
Collaboration across functions
Stakeholder and external engagement
Embraces diversity and equality
Key Requirements
Bachelor's degree in Engineering
Minimum of three (3) years related experience
Thorough knowledge of pharmaceutical/medical device manufacturing
Project management experience and proficiency
Knowledge of project management and change control