Perform validation engineering tasks, Review protocol drafts and resolve conflicts and concerns in order to achieve management pre-approval. Coordinate the execution of qualifications and all aspects of the validation project with other departments, including but not limited to: Operations, Engineering, Quality Control and Quality Assurance. Perform or supervise the execution of protocols and maintain documentation as evidence of compliance with current Good Documentation Practices. Review, analyze and compile protocol data and write reports for management review and approval. Perform and document risk assessments to determine validation strategy and approach. Ensure processes and products are in compliance with all local, state, and federal rules and regulations. Oversee that processes are in CGMP compliance and establish systems that identify opportunities for improvement and make constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as, USDA, cGMPs, EudraLex, and other regulatory agencies. Work under supervision. Travel And/Or Relocation to unanticipated client sites in USA is required.

Master's degree in Pharmacy, Chemistry, Science, Engineering(any) or closely related field.

Perform validation engineering tasks, Review protocol drafts and resolve conflicts and concerns in order to achieve management pre-approval. Coordinate the execution of qualifications and all aspects of the validation project with other departments, including but not limited to: Operations, Engineering, Quality Control and Quality Assurance. Perform or supervise the execution of protocols and maintain documentation as evidence of compliance with current Good Documentation Practices. Review, analyze and compile protocol data and write reports for management review and approval. Perform and document risk assessments to determine validation strategy and approach. Ensure processes and products are in compliance with all local, state, and federal rules and regulations. Oversee that processes are in CGMP compliance and establish systems that identify opportunities for improvement and make constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as, USDA, cGMPs, EudraLex, and other regulatory agencies. Work under supervision. Travel And/Or Relocation to unanticipated client sites in USA is required.

Master's degree in Pharmacy, Chemistry, Science, Engineering(any) or closely related field.