Currently Working As A Documentation Controller At Quality Assurance Deparment In Swiss Pharmaceuticals (Pvt.) Ltd (Joining Date: 01-07-2019)
Standard Operating Procedure 
Quality Format
Batch Manufacturing Record
Batch Processing Record
Certificate of Analysis 
Analytical data Record
Finish Product Specification
Master Data Record
Maintain Reference Samples
Standard Testing Method
Duties & Responsibilities  
To Assist QA/ QC Associates In Performing Their Duties Regarding 
Documentation and Record Control.
To Perform All The Activities Of Documentation And Record Control (D&RC)
According To Relevant SOP.
Receive Intimations From Production/ Warehouse, And Enter In Master Control
Register And Assign The QC. Ref. No.
Assign QC Ref. No. To All Products According To Procedure And Enter In  
Relevant BMR And Register.
Compile Batch Wise Record Of The Entire Product.
Receive The BMR/BPR/QC Report From Production & QC And Submits The 
BMR/BPR/QC Report To Production After Final Audit And Maintain The Record Accordingly. 
Compile Certificate Of Analysis. Of The Products For Records 
Prepare Daily Progress Report And Submit To Head Of Quality For Onward
Submission.
Receive Reference And Stability Sample, Place Safely And Securely In
Reference Room And Maintain The Record.
To Ensure The Implementation Of The Requirements Of GDP And Quality
Management System.
Ensure That All The Record Is Readily Available.
1 Year Work At Warehouse In Paul Brooks Homeo Labs.
Dispensing Of Raw Material.
Sampling And Analysis Of Packing Material.
Dispensing Of Herbal Material.