Regulatory Affairs Department Head (Pharmaceutical)
Legal & ComplianceOtherRegulatoryRegulatory Affairs
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Quick Summary
Overview
Location: Laguna Work Schedule: Monday to Friday, 8:00 AM to 5:00 PM Set Up: Onsite role About the Role The Regulatory Affairs Department Head will oversee all regulatory submissions, renewals,
Technical Tools
Legal & ComplianceOtherRegulatoryRegulatory Affairs
Location: Laguna
Work Schedule: Monday to Friday, 8:00 AM to 5:00 PM
Set Up: Onsite role
About the Role
The Regulatory Affairs Department Head will oversee all regulatory submissions, renewals, and compliance initiatives for both local and export markets. You will manage a small team, guide regulatory strategy, and collaborate closely with cross-functional departments to ensure timely and accurate documentation.
This role plays a critical part in ensuring the organization meets all regulatory standards while supporting client requirements and maintaining up-to-date knowledge of industry regulations.
Key Responsibilities
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Lead the regulatory team in managing product registrations, renewals, and compliance activities.
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Review and approve technical dossiers for local and international submissions.
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Coordinate with Technical Services, QA, QC, Formulation, Marketing, and other internal groups to ensure complete documentation.
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Liaise with regulatory agencies and client regulatory counterparts.
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Monitor regulatory changes and provide updates to internal stakeholders.
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Serve as the Pharmacovigilance Officer and ensure adherence to reporting requirements.
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Maintain updated databases of regulatory documentation and regional requirements.
Leadership Responsibilities
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Direct management of a Regulatory Affairs Manager, Regulatory Affairs Associate, and Company Pharmacist.
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Oversight of an indirectly supervised Technical Clerk.
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Work under general supervision of the R&D/Regulatory Division leadership.
Qualifications
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Licensed Pharmacist with a degree in Pharmacy or Industrial Pharmacy.
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Minimum of 5 years of experience in regulatory affairs or product registration within manufacturing (pharmaceutical, food, or cosmetics preferred).
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Strong understanding of FDA regulations and other government regulatory frameworks.
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Knowledge of GMP, ISO 9001:2015 basics, EHS, QMS, and licensing processes.
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Excellent attention to detail, documentation skills, and communication abilities.
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Proficiency in basic computer applications.
Additional Skills
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Strong problem-solving and decision-making capability
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Root cause analysis
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Project management
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Customer service orientation
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Performance management
Working Environment
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Clean, well-organized office setup
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Hybrid of desk work and occasional field activities
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Collaboration with internal teams and external regulatory bodies
Location & Eligibility
Where is the job
Santa Maria, Philippines
On-site at the office
Who can apply
PH
About this job
- Who can apply
- Philippines
- Posted
- 30 days ago
Listing Details
- First seen
- September 25, 2026
- Last seen
- October 26, 2026
Posting Health
- Days active
- 30
- Repost count
- 0
- Trust Level
- 19%
- Scored at
- October 26, 2026
Signal breakdown
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