Section Manager of Validation
We are seeking an experienced validation professional for a parenteral drug firm who will, through a staff of five people, provide leadership for equipment, process and utility systems validation.
Specific areas of responsibility include development/maintenance of documentation systems, SOP's, IQ, OQ, PQ and protocols, interface on investigations and corrective actions, development of Master Validation Plans, remediation activities, and allied areas.
The qualified candidate will have a BS degree minimum in a technical, engineering or scientific discipline, five years or more of validation experience, at least two of which have been spent in a leadership/supervisory capacity, experience dealing with FDA personnel - advanced degrees and/or certifications a plus.
This position is immediately open due to the promotion of the incumbent.
Salary:
$100,000.
00 - $110,000.
00.
Estimated Salary: $20 to $28 per hour based on qualifications.
Specific areas of responsibility include development/maintenance of documentation systems, SOP's, IQ, OQ, PQ and protocols, interface on investigations and corrective actions, development of Master Validation Plans, remediation activities, and allied areas.
The qualified candidate will have a BS degree minimum in a technical, engineering or scientific discipline, five years or more of validation experience, at least two of which have been spent in a leadership/supervisory capacity, experience dealing with FDA personnel - advanced degrees and/or certifications a plus.
This position is immediately open due to the promotion of the incumbent.
Salary:
$100,000.
00 - $110,000.
00.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
