Bachelor’s degree in Engineering, Life Sciences, or related technical field
- 5+ years of experience in pharmaceutical solid oral dose manufacturing
- Basic understanding of cGMP or regulated industry practices
- Strong troubleshooting and problem-solving skills
- You bring a positive, professional attitude and can communicate and collaborate with all levels of employees, customers, contractors & vendors.
- Comprehensive knowledge of Regulatory and cGMP guidelines, with the ability to contribute to quality records (Deviations, Investigations, CAPA, and Change Control).
