cGMP Consulting Inc., founded in 2001, specializes in helping clients adopt new technologies and comply with Good Manufacturing Practices (cGMP). With a team of experienced engineering and quality assurance consultants, the company offers a range of services including equipment qualification, validation master plans, process validation, and FDA regulatory compliance. They excel in identifying gaps, supporting international pharmaceutical manufacturing, and implementing cGMP requirements to ensure client success.
Open Positions
Senior Cleaning Validation Engineer
4+ years of experience in GMP manufacturing environment, including cleaning validation, with a Bachelor's degree in Engineering, Science, or a related field of study
MIT Engineer
Bachelor's degree in Engineering, Science, or a related field, 3+ years of experience in regulated manufacturing environments, and strong troubleshooting and communication skills
Senior Engineer
Bachelor's degree in Engineering, Science, or a related field of study, 5+ years' experience in a GMP manufacturing environment, expertise in multiple areas including cleaning validation, qualification of aseptic filling or formulation equipment/processes, and packaging
Engineer I
Bachelor's degree in Engineering, Science, or related field; 0-2 years' experience in GMP manufacturing environment; Technical writing and regulatory knowledge preferred
Engineer II
2-5 years of experience in a GMP manufacturing environment, Bachelor's degree in Engineering, Science, or a related field of study
Automation CQV Lead
5+ years experience in GMP manufacturing environment, strong knowledge of validation lifecycle practices, deviation/investigation workflows, and data integrity principles
Project Manager
Minimum 4 years’ experience in a GMP manufacturing environment, Bachelor's degree in Engineering, Science, or a related field of study, and PMP, CAPM, or equivalent project management certification