Manage the Testing and release / reject incoming Raw / Packing Materials, in-process stage up to FG as per quality Plan & Respective Finished product Specification and forward the data for QA Authorisation.
Maintain list of calibrated equipment's and carried out as per schedule by Nationally recognized agencies.
Maintain clean room facility like cleaning and Fumigation process regular basis.
Testing carried out environmental monitoring testing and per ISO 14644-1 and Schedule- M requirements.
Prepare Monthly reports, investigate and initiate corrective and preventive actions and monitor clean room environmental monitoring testing paraments.
Prepare Monthly reports, investigate and initiate corrective and preventive actions and monitor Quality trends and environmental monitoring.
Testing carried out inspection of the In-process checks from Prime to Final packing and ensure strict compliance to Quality Plan and Procedures.
To identify non-conformances and ensure avoidance of further processing of non-conforming products before rectification.
To ensure good housekeeping, safety and correct usage of equipments.
To ensure proper documentation and maintenance of quality records.
To review and upgrade Methods, specification as per data available with QC lab.
Clean room Environmental Monitoring.
To ensure that the requirements of ISO 13485:2016, Medical Device Rule,2017, ISO 3826-1:2013, USFDAp QSR - CFR Part 820 and such other international standards are implemented and maintained.
Such other assignments the Management may give from time to time.
This job description is subject to change by the Management to suit changing requirements from time to time.
This does not restrict Management's right to change assignments under its Job Rotation Policy to suit company's requirements and / or individuals growth opportunities.
Job Types: Full-time, Permanent
Pay: ?12,000.00 - ?15,000.00 per month
Work Location: In person
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