Ahmedabad · Internship
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HIGH
Our tracked job listings for Troikaa Pharmaceuticals show strong recent activity.
First 72 hours
Window passed - posted 587d agoEarly applicants get seen before the pile builds.
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The first time we've seen this listing - it hasn't been closed and reopened.
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QMS documents initiation and review:
QMS documents initiation for QC.
Responsibilities
SOP preparation, review and tracking till closing the CCF.
Initiation of Change control for departmental activity, to perform the assessment of departmental / cross
functional department CCF, to perform impact assessment. To ensure the closure of CCF within the timeline.
To give the ADS of Logbook, worksheet and formats.
To tracking the Logbook, Specification and Method of Analysis, SOP.
Training
To schedule training in LMS.
To prepare Job responsibility and update in LMS.
General
To ensure the current version method of analysis and specification available.
To follow good laboratory practices
To attain the training in LMS software before due date.
To verify and record the cleaning of quality control area.
To participate in investigations of OOS/ laboratory incident / OOT/ deviation.
To inform the section In charge for the break-down of equipment.
Immediately information to the In-charge-QC in case of any abnormal observation found during analysis
Any data integrity related observation in the department shall be bring to notice of QC-Head.
To maintain the discipline in laboratory
Any other work assigned by section head / Head-QC.
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