Experience 9-10 Years in Regulatory Affairs and QC/QA.
Prepare & Process applications (product dossiers) of imported or locallymanufactured drugs with DRAP for registration/enlistment andchanges/corrections/transfer etc.
Communicate and correspond with foreign principals on regulatory matters andprocurement of product dossiers, other regulatory and import documents fromthem.
Prepare and scrutinize import documents for DRAP's & Customs' clearance.
Undertake technical evaluation and training of product(s).
Ensure pharmaceutical Quality control and quality assurance.
Maintain close liaison with DRAP, Health & Other Regulatory Departments/ Agencies.
D Pharmacy Degree is Must for thisJob.
Please send their CV at mentioned below email IDJob Expired
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|Job Posted||Apr 16, 2022|
|Job Type||Full time|
|Job Company||Hi Tech Pharmaceuticals Pvt Ltd|
|Job Experince||10 year|
|Job Salary||PKR Compatible / Month|
|No of Openings||1 opening|
|Job Daedline||May 16, 2022|