RIO Execution Hub Manager
Pfizer
full-time
Posted on:
Location Type: Hybrid
Location: Makati City • 🇵🇭 Philippines
Visit company websiteJob Level
Mid-LevelSenior
About the role
- Provide regulatory support to the International country and/or cluster Regulatory teams.
- Support numerous regulatory activities;
- Act as initial point of contact for assigned Country/Cluster for key stakeholders.
- Identification of regulatory requirements,
- Authoring, delivery and/or coordination of local, submission-ready documents
- Quality review/approval of the Dossier provided by Hub Submission/Dossier Managers.
- Ensure timely delivery of local M1 dossier components.
- Provide support for local audit readiness activities.
- Partner with Grow submission managers and Regional Submission Hubs to deliver applications.
- Lead regulatory support to countries/clusters.
Requirements
- B.S./B.Scs. is in Pharmacy, Life Sciences, Business or Information Technology (desirable);
- Advanced to Fluent English language required.
- Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.
- Advanced Microsoft Office Suite skills.
- Familiarity with pharmaceutical organizational structures, systems, and culture.
- An understanding of country/cluster regulatory requirements and trends is preferred.
- Relevant experience within pharma, in Regulatory, quality and/or compliance fields.
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
regulatory supportauthoring documentsquality reviewaudit readinesssubmission-ready documentsregulatory requirementscompliancetechnical aptitudepharmaceutical regulationsquality standards
Soft skills
communicationstakeholder managementorganizational skillsleadershipcollaborationproblem-solvingadaptabilityattention to detailtime managementinterpersonal skills