Posted:4 weeks ago|
Platform:
On-site
Part Time
Maintain self-hygiene and ensure compliance with cGMP, GDP and departmental discipline.
Prepare and review the master documents, protocols and reports of production as per requirements.
Manage the Exhibit batch documents such as BMRs, BPRs, etc.
Handle change control, deviations, CAPA, investigation, etc.
Train all the subordinates, technicians and operators of the department.
Perform other activities as per HOD’s requirement and guidance.
Attend and ensure training as per training schedule and TNI.
Review BMR, BPR and other Exhibit batch related documents.
Skills:
Change control, deviations, CAPA, investigation, BMR, BPR, SOP.
Qualification - B. Pharm
Amneal Pharmaceuticals
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