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).