Interview Data Loading …Looking for QC Head for Panoli - (Gujarat Location)
Minimum - 12-15 Yrs
Responsibilities:[ads id="ads1"] To ensure proper Gowning procedure during entry and exit in working area as per SOP.
To ensure CGMP compliance.
To ensure proper Receipt of AMT samples & analysis plan.
Responsibilities to approve the job description and assigned the job to all the section personals.
To review and approve the AMT/AMV protocols and reports.
To ensure the schedule trainings and development of analyst.
To ensure completion of analysis for analytical method validation and process validation within the time period.
To check & sign the reports & documents.
To prepare daily & monthly reports with status.[ads id="ads2"] Co-ordination with R&D/outside labs from where product is transferred at site.
Monitoring the samples to be sent external labs for testing in which testing facility is not available.
Responsibilities to release the and OOT, deviations, change control and CAPA within stipulated time.
Coordination with Quality Assurance department.
Responsibility to conduct the training of all the section chemists on routine basis.
Responsibility of the laboratory in personals to follow the compliance.
Training and development of officers/Executives.
batches (RM/FG/PM) within required time.
Investigate related to OOS, OОЕ,
share resume on hrd@amgislifescience.com
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Interview Data Loading …
Looking for QC Head for Panoli - (Gujarat Location)
Minimum - 12-15 Yrs
Responsibilities:
[ads id="ads1"]
To ensure proper Gowning procedure during entry and exit in working area as per SOP.
To ensure CGMP compliance.
To ensure proper Receipt of AMT samples & analysis plan.
Responsibilities to approve the job description and assigned the job to all the section personals.
To review and approve the AMT/AMV protocols and reports.
To ensure the schedule trainings and development of analyst.
To ensure completion of analysis for analytical method validation and process validation within the time period.
To check & sign the reports & documents.
To prepare daily & monthly reports with status.
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Co-ordination with R&D/outside labs from where product is transferred at site.
Monitoring the samples to be sent external labs for testing in which testing facility is not available.
Responsibilities to release the and OOT, deviations, change control and CAPA within stipulated time.
Coordination with Quality Assurance department.
Responsibility to conduct the training of all the section chemists on routine basis.
Responsibility of the laboratory in personals to follow the compliance.
Training and development of officers/Executives.
batches (RM/FG/PM) within required time.
Investigate related to OOS, OОЕ,
share resume on hrd@amgislifescience.com
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