Registrered pharmacist

Requirements:

Graduate of Bachelor Science in Pharmacy.

A registered Pharmacist

Preferably with atleast 1 year work experience in handling product registration BFAD/FDA Fresh graduates may apply

With excellent communication skills computer literate in MS Word, Excel and Powerpoint.

Job Responsibilities:

1. Maintain and align the company with the different changes in the Philippine laws and constitutions and FDA regulations and administrative orders;
2. Update the company on any new FDA rules and regulations and other relevant public information;
3. Coordinate with the Toll Manufacturer’s Research and Development Department for Product Development updates when as needed;
4. Coordinate with MPSI Purchasing Head for the acquisition of some active raw materials as ingredient of the pharmaceutical product for toll manufacturing;
5. Assessment of active raw material quality thru the supplier’s certificate of analysis from its manufacturers prior to order or purchasing;
6. Check and monitor the availability and validity of Government Licenses of the local Raw Material Suppliers and determine its accreditation at FDA;
7. Random inspection of Product Inventory and Distribution Record to check for compliance of company’s Standard Operating Procedures and recording rules for traceability;
8. Check the daily monitoring and continuous compliance of Standard Operating Procedures in Warehouse operations;
9. Carry-out Self-inspection in the company with its observance in proper warehouse operations and maintenance is fully and effectively implemented to assess the GMP, DSP and GSP Compliance;
10. Conduct random cGMP inspection / audit to Toll Manufacturers, Distributors, RM and PM vendor suppliers, in alignment with Pharmaceutical Inspection Co-operation Scheme Good Manufacturing Practices PE009-14;
11. Attend to Licensing seminars and certifications provided by FDA and authorized organizations;
12. Update oneself to the dynamic changes in Pharmaceutical Industry Practices;
13. Coordinate with Warehouse Personnel in the implementation of new FDA rules and administrative orders;
14. Check the quantity of box and products that have been picked up by the company driver and warehouse assistants from Toll Manufacturer;
15. Check the products before delivery to distributors;
16. Assessment of product replacements and complaints regarding its physical properties;
17. Assessment of packaging labels and materials using color standard filings as basis;
18. Responsible for complying FDA rules and regulations concerning company operations as Drug Trader;
19. File and document technical information of all active ingredients of the products in relevant to the needs of Medical Director;
20. Update GS1 account for addition of new product barcode or for migrating to 2D barcodes;
21. Submission of Semi-annual Report 2x a year, S-license Renewal annually, and Local Order Permit to PDEA when as needed;
22. Monitor IPOPHIL Trademark certificates and DAU applications;
23. Process for the renewal of MIMS and PPD product listing.