REGULATORY PHARMACISTZurerx Corp

JOB DESCRIPTION
Updates and compiles Manufacturing and Distribution contracts for all suppliers and manufacturers.
Request for Drug Assay of each product at CEDRES or UP-NIH twice a year to ensure that all products are of good quality and complies with claimed dosage strength.
Coordinates with suppliers with regards to the basic accreditation documents like CGMP (Certificate of Good Manufacturing Practice) certificate requests, company and product profile and other regulatory documents.
Checks product insert and packaging material of each product to make sure it complies with FDA’s specifications.
Coordinates with suppliers if there are corrections/clarifications until the final product packaging is achieved.
Coordinates with MIMS re: product monographs of products to be included in the print-out and on MIMS online.
Attend required trainings and seminars for renewal of pharmacist license (including CPD seminars with a total of 45 units per 3yrs).
JOB QUALIFICATION
1
year(s) general experience related to Product Development responsibilities
2
year(s) general experience related to Product Development responsibilities
1
year(s) supervisory experience related to Regulatory responsibilities
2
year(s) supervisory experience related to Regulatory responsibilities
3
year(s) of specific experiences Regulatory responsibilities
 With PRC license
OTHER JOB REQUIREMENTS
Education
Bachelor's/College Degree
Field of study
Pharmacy/Pharmacology
Specialization
Pharmacy
Customer Care, Record Keeping