0 - 3 years
2 - 3 Lacs
Posted:1 day ago|
Platform:
On-site
Full Time
Verification & Authorization:- Verification & authorization of Q.C. documents, Q.C. & Production Process, Sample storage to ensure execution of production & Q.C. process as per SOP.
Analysis & Control:- To collect data, analysis & calculate Std data, Prepare/Modify SOP to improve production & q.c. process.
Monitor & Supervise:- Daily monitoring and supervise Q.C. process to achieve on time Test reporting by following Schedule-T
Documents:- To verify & authorize production & Q.C. documents, Q.C. Live reports, submit & ensure approval FDA Documents to achieve 100% legal compliance as per the FDA norms.
Reporting:- Daily/Weekly/Monthly reporting of various production & Reports to Plant Mgr. in order to confirm legal compliance as per Schedule-T.
Continues Improvement:- Establishing managing, Planning, Scheduling and executing analytical method validation and analytical method development or improvement programs for existing R.M. & F.G. in order to improve quality/productivity/safety by following GMP norms.
Technical Support:- Give technical support to our customer, visitors, employee to achieve quality product & customer satisfaction by following Schedule-T.
Qualification-MSC , BSC or B.Pharm
Experience-0 to 3 Years
Job Types: Full-time, Permanent, Fresher
Pay: ₹17,000.00 - ₹30,000.00 per month
Benefits:
Work Location: In person
Precise Chemipharma Pvt Ltd
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