Regulatory Affairs Project Staff

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At Getz Pharma, our mission is to make a global impact by developing and delivering safe, effective, and high-quality medicines that improve the lives of men, women, and children. Be part of a company where your work directly contributes to better health outcomes and a healthier world. Why Join Getz Pharma as a Senior Regulatory Affairs Specialist? Drive...

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...

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,...

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,...

4 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Meralco PowerGen (MGEN) Overview The Head of Regulatory Management will lead Meralco PowerGen’s regulatory strategy, legal compliance, and engagement with government agencies, industry associations, and key...

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...

Overview Gather data, conduct research, and site investigation for various sectoral projects. Work closely and collaboratively with the project team, experts, and other professionals to ensure delivery of project requirements. Create reports, letters, and documents at a timely pace. Review and critique technical reports submissions. Attend intra-project,...

Overview ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven...

Bachelor of Science in Pharmacy (BS Pharmacy)Must be a licensed Pharmacist (PRC board passer)1–2 years of relevant experience, preferably in the pharmaceutical industryKnowledge of FDA regulations and handling of controlled substancesExperience in Regulatory Affairs and Product Inventory ManagementStrong communication skills with a proactive,...