Posted:18 hours 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-M.pharm or B.Pharm
Experience-2 to 3 Years of independent lab handling
Skills- Inspection, People Management, Team Handling, Lab Management.
Analytical Thinking, Problem Solving, Verbal Communication, Written Communication
#QC#NASHIKJOBS#QA#PHARMA#TESTING#LABS
Job Types: Full-time, Permanent
Pay: ₹25,000.00 - ₹27,000.00 per month
Benefits:
Ability to commute/relocate:
Education:
Experience:
Chaitanya Pharmaceuticals Pvt. Ltd, Nashik
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