Regulatory Affairs Department Head (Pharmaceutical)
OtherRegulatory Affairs
2 views0 saves0 applied
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
OtherRegulatory 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
-
Lead the regulatory team in managing product registrations, renewals, and compliance activities.
-
Review and approve technical dossiers for local and international submissions.
-
Coordinate with Technical Services, QA, QC, Formulation, Marketing, and other internal groups to ensure complete documentation.
-
Liaise with regulatory agencies and client regulatory counterparts.
-
Monitor regulatory changes and provide updates to internal stakeholders.
-
Serve as the Pharmacovigilance Officer and ensure adherence to reporting requirements.
-
Maintain updated databases of regulatory documentation and regional requirements.
Leadership Responsibilities
-
Direct management of a Regulatory Affairs Manager, Regulatory Affairs Associate, and Company Pharmacist.
-
Oversight of an indirectly supervised Technical Clerk.
-
Work under general supervision of the R&D/Regulatory Division leadership.
Qualifications
-
Licensed Pharmacist with a degree in Pharmacy or Industrial Pharmacy.
-
Minimum of 5 years of experience in regulatory affairs or product registration within manufacturing (pharmaceutical, food, or cosmetics preferred).
-
Strong understanding of FDA regulations and other government regulatory frameworks.
-
Knowledge of GMP, ISO 9001:2015 basics, EHS, QMS, and licensing processes.
-
Excellent attention to detail, documentation skills, and communication abilities.
-
Proficiency in basic computer applications.
Additional Skills
-
Strong problem-solving and decision-making capability
-
Root cause analysis
-
Project management
-
Customer service orientation
-
Performance management
Working Environment
-
Clean, well-organized office setup
-
Hybrid of desk work and occasional field activities
-
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
Listing Details
- First seen
- September 25, 2026
- Last seen
- October 6, 2026
Posting Health
- Days active
- 10
- Repost count
- 0
- Trust Level
- 33%
- Scored at
- October 6, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
External application
Similar Regulatory Affairs jobs
View all →Browse Similar Jobs
Newsletter
Stay ahead of the market
Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.
A
B
C
D
No spam. Unsubscribe at any time.