, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined... and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP...
' experience in consulting and/or engineering services. Bachelor's Degree in Life Science, Engineering, or related discipline... (OR a combination of equivalent work experience in CQV engineering, cGMP facility start-up, project management and/or comparable...
and Experience Required: 5-7 years' experience in consulting and/or engineering services. Bachelor's Degree in Life Science..., Engineering, or related discipline (OR a combination of equivalent work experience in CQV engineering, cGMP facility start-up...
Payrate: $24.00 - $27.00/hr. Summary: This role will ensure that raw materials received for use in our cGMP... & sampling results are complete and detailed according to written procedures and cGMP requirements Responsible for accurately...
in . In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting... and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP...
in . In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting... and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP...
compliance with design intent, specifications, cGMP standards, and schedule. Review RFIs, submittals, redlines, shop drawings... (preferred but not required). Knowledge of GMP, FDA/EMA expectations, and engineering documentation practices. Prior consulting...
characteristics needed for our cGMP manufacturing processes. The role also involves leadership in scheduling, coordination, and staff... are complete and detailed according to written procedures and cGMP requirements. Accurately document inspection, sample, and test...
candidates need apply. 100% onsite 3 Key Consulting is hiring a Engineer, Drug Product Process Development and Tech Transfer... Project Support for a consulting engagement with our direct client, a leading global biopharmaceutical company...
audits of inter-departmental validation programs. Selects bidders, awards and administers contracts involved for consulting... Good Manufacturing Practices (cGMP) compliance as the validation representative on engineering project teams. Develops...