Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist
Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist
regular audits and inspections of production facilities to identify and resolve any quality or safety
monitor performance of GMP and PRP programs in the facility Identify quality control points within processes
monitor performance of GMP and PRP programs in the facility Identify quality control points within processes
are proud of our clean, technological advanced facility and we encourage our clients and partners to come
knowledge
3 Years experience in an ISO 17025 accredited facility Practical experience in an ISO 17025 laboratory
3 Years experience in an ISO 17025 accredited facility Practical experience in an ISO 17025 laboratory