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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).