Job Description
Description
Follow and handle all quality and compliance activities according cGMP, FDA, and ISO 13485 activities Approve and release all batch records and raw materials Review and handle all deviation and investigations Support and help to handle any regulatory audits in QMS
Skills
compliance management, compliance, Quality assurance, batch record review, deviation, investigations, root cause analysis, Gmp, batch record, Document control, quality management system, iso 13485
Top Skills Details
compliance management,compliance,Quality assurance,batch record review,deviation,investigations,root cause analysis
Additional Skills & Qualifications
BS in a life science and 3-5 years' experience Experience working in GMP, FDA, and ISO requirements Experience working in Quality Management systems
Experience Level
Intermediate Level
Job Type & Location
This is a Contract position based out of Bedford, MA.
Pay ...
Follow and handle all quality and compliance activities according cGMP, FDA, and ISO 13485 activities Approve and release all batch records and raw materials Review and handle all deviation and investigations Support and help to handle any regulatory audits in QMS
Skills
compliance management, compliance, Quality assurance, batch record review, deviation, investigations, root cause analysis, Gmp, batch record, Document control, quality management system, iso 13485
Top Skills Details
compliance management,compliance,Quality assurance,batch record review,deviation,investigations,root cause analysis
Additional Skills & Qualifications
BS in a life science and 3-5 years' experience Experience working in GMP, FDA, and ISO requirements Experience working in Quality Management systems
Experience Level
Intermediate Level
Job Type & Location
This is a Contract position based out of Bedford, MA.
Pay ...