Regulatory Affairs Pharmacist

Regulatory Pharmacist Rivermed, Inc Salary: ₱25-30K (Monthly) On-site - Pasig Experience: 1-3 Yrs Exp Bachelor Full-time Job Description Prepare, review, and submit product registration dossiers to the FDA (Food and Drug Administration) and other relevant regulatory bodies. Ensure all products comply with local laws and regulations, including labeling,...

QUALIFICATIONS:Licensed PharmacistPreferably with at least one year of experience in regulatory affairs.Knowledge of ACTD is an advantage.DUTIES & RESPONSIBILITIES:Responsible for the review and submission of drug product dossiers.Responsible for reviewing and submitting GMP dossiers.Responsible for product selection from existing partner...

Key Responsibilities Handle product registration, renewal, and variation applications for submission to the FDA and other relevant agencies. Ensure compliance with all applicable pharmaceutical and medical device regulations. Prepare, review, and maintain regulatory documents, licenses, and certificates. Coordinate with internal departments, manufacturers,...

This position involves managing regulatory submissions, maintaining compliance documentation, and liaising with regulatory agencies to facilitate product approvals. The ideal candidate will possess strong knowledge of regulatory affairs, attention to detail, and the ability to navigate complex regulations in the pharmaceutical, biotechnology, or medical...

JOB LOCATION: KAPITOLYO PASIG CITYJOB REQURIEMENT: LICENSED PHARMACISTJOB SUMMARY: Under the direct supevision of the Regulatory Affairs Manager, the Regulatory Affairs Pharmacist assists the manager in ensuring that all regulatory documents required by government agencies are accomplished and submitted on time. This position is responsible for preparing,...

Job Description:Perform various functions pertinent to preparation of regulatory documents and documents for product registrationPerform liaison activities at the Food and Drug AdministrationProvide sales department requests such as LTO, CPR and other related documentsEdit labelling requirements in accordance to FDA guidelinesQualifications:Candidate must...

Job SummaryThe Regulatory Specialist ensures that the company complies with all applicable FDA regulations on licenses, product registration, internal and external audit and inspection, technical documentation and monitoring and trainings on product knowledge, pharmacovigilance, Good Storage and Distribution Practices, Current Good Manufacturing Practice,...

About the RoleThis position involves managing regulatory submissions, maintaining compliance documentation, and liaising with regulatory agencies to facilitate product approvals. The ideal candidate will possess strong knowledge of regulatory affairs, attention to detail, and the ability to navigate complex regulations in the pharmaceutical, biotechnology,...

JOB DESCRIPTION - REGULATORY PHARMACISTPrepare and submit documents to FDA such as license to operate, document for initial registrations, product registrations, GMPs, clearance applications, renewal of CPR including variation and compliance of existing product.Monitor the status of applications with FDAChecks updates and reports on regulatory input by...

Senior Regulatory Specialist Ensure that the Regulatory Department is doing their assigned duties and responsibilities Direct reporting to General Manager and Regulatory Affairs Head from parent company Food Registrations (FDA) – preparation of documents and actual sample for submission Initial Applications Renewal Applications Reapplications (submissions...