Piramal Pharma Job Vacancy For Quality Control Dept
Position: Executive-Quality Control
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| Piramal Pharma Job Vacancy For Quality Control Dept |
Position: Executive-Quality Control
Location: Navi Mumbai, Maharashtra, India
Qualifications: M.Sc. Analytical Chemistry with relevant experience.
Job Responsibilities:
To prepare, review and update SOP, Specification, Method of analysis, report and protocol.
To review the documents such as inprocess, intermediate, cleaning validation, water reports as per cGMP.
To attend the trouble shooting of QC instruments and to co-ordinate with the authorized supplier for support if any.
To check the training program are conducted as per training schedule.
To maintain, execute and update calibration and validation schedule of all QC instrument.
To ensure the cGLP practices are followed in QC department.
Handling change control related documentation in QC department.
Monitoring the procedures related to Laboratory management is followed as per SOP.
Involved in investigations like Deviation, OOS, OOT etc.
Ensuring completion of investigations with documentation within the specified timeframe.
Ensuring that the CAPA implementation and effectiveness review in QC department.
In absence of employee deputy person handle the above responsibility.
Qualifications: M.Sc. Analytical Chemistry with relevant experience.
Job Responsibilities:
To prepare, review and update SOP, Specification, Method of analysis, report and protocol.
To review IQ, OQ, PQ of new instrument.
To review the documents such as inprocess, intermediate, cleaning validation, water reports as per cGMP.
To attend the trouble shooting of QC instruments and to co-ordinate with the authorized supplier for support if any.
To check the training program are conducted as per training schedule.
To maintain, execute and update calibration and validation schedule of all QC instrument.
To ensure the cGLP practices are followed in QC department.
Handling change control related documentation in QC department.
Monitoring the procedures related to Laboratory management is followed as per SOP.
Involved in investigations like Deviation, OOS, OOT etc.
Ensuring completion of investigations with documentation within the specified timeframe.
Ensuring that the CAPA implementation and effectiveness review in QC department.
In absence of employee deputy person handle the above responsibility.
Click on below link for apply
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