Description
DESCRIPTIONThe Senior Validation Engineer will coordinate with Operations to perform CIP PQ.
Responsibilities:
CIP PQ and Cleaning Monitoring Samples
Generate pre-approval CIP PQ packages and get them approved.
Coordinate with Engineering Management and Quality to review and approve the package.
Generate and resolve the deviations with help from Engineering Management and Quality.
Create and update the status tracking spread sheet to communicate the status of the CIP PQ.
Generate and facilitate review the summary report. If the CIP PQ sampling can be used for annual cleaning monitoring sample, complete the cleaning monitoring form with the same set of cleaning samples from the CIP PQ.
Cleaning Changeover at the End of Campaign.
Generate pre-approval cleaning change over packages and get them approved Coordinate with Operations to perform cleaning change over.
Coordinate with Engineering Management and Quality to review and approve the package.
Generate and resolve the deviations with help from Engineering Management and Quality
Generate and facilitate review the summary report.
If the cleaning change over sampling can be used for annual cleaning monitoring sample, complete the cleaning monitoring form with the same set of cleaning samples from cleaning change over.
*THIS IS A SENIOR LEVEL ROLE; 7 TO 10 YEARS EXPERIENCE REQUIRED
SKILLS
Manufacturing, Pharmaceutical
Synectics is an Equal Opportunity Employer.