Unilab is the leading pharmaceutical company in the Philippines, and it remains to be a strong industry leader distinguished by its values of Husay, Malasakit at Bayanihan.

Currently, Unilab is home to more than 300 brands of affordable top-quality products in all the significant therapeutic categories, such as prescription drugs, consumer healthcare, and personal care products. We care for millions of Filipinos with trusted brands such as Biogesic, Enervon, Neozep, Alaxan, Bioflu, Myra-E, Ceelin, and others.

Lead with Purpose. Experience Alagang Unilab.

For 80 years, Unilab has remained steadfast in its purpose: to build a healthier Philippines, one quality medicine at a time. Guided by our deeply rooted values of Husay at Malasakit and the spirit of Bayanihan, we continue to serve Filipino communities by providing them trusted quality healthcare.

At the core of everything we do is Alaga—the heart of our brand and culture. We ensure that our people genuinely feel this care, so they can extend the same compassion and commitment to the communities we serve, making quality healthcare more accessible to every Filipino.

We believe that when our people feel genuinely cared for, they are empowered to care more deeply for others. That’s why we invest in our people through meaningful work, continuous learning, supportive leadership, holistic well-being, and a collaborative environment.

When you join Unilab, you don’t just build a career—you lead with purpose. You create real impact by delivering quality healthcare to Filipinos, and in the process, you also experience Alagang Unilab—through personal growth and professional development. 

Unilab, Inc.

Regulatory 
• Prepares and submits product registration dossiers to the Philippine FDA. 
• Evaluates dossiers for quality and completeness. 
• Prepares and submits product registration dossiers to export country affiliates/distributors. 
• Maintains Licenses to Operate and Certificates of Foreign Good Manufacturing Practice with the FDA. 
• Handles promotional permit applications and submits to the FDA. 
• Coordinates with regulatory agencies on registrations, variations, and permits. 
• Manages product information in various databases. 
• Prepares and reviews procedural documents for FDA submissions and commercial orders. 
• Ensures valid processes for packaging transitions. 
• Provides customer support for product inquiries and transport documents.

Medical - Strategic Marketing Support: 
• Handles packaging artworks for product registration or promotions. 
• Manages pharmacovigilance activities and reports adverse events to the FDA. 
• Coordinates quality-related complaints and suspected counterfeit products. 
• Supports marketing efforts with necessary documents.

Medical Education Programs: 
• Prepares educational materials for divisional programs. 
• Implements medical training for personnel and partners.

Advertising Claims Support: 
• Researches and provides medical information for product claims and brand communication. 
• Reviews and updates packaging text for relevant claims. 
• Assists in filing complaints against competitor products. 
• Coordinates product inclusion in medical directories (MIMS, PPD).

Regulatory Affairs Specialist

• Ensures proper documentation and storage of drug samples for Comparative Dissolution Profile (CDP) testing and Bioequivalence (BE) studies and coordinates receipt and dispatch of drug samples 
• Manages and documents the handling and storage of investigational products for Clinical Studies 
• Reproduces, organizes and packs the approved study materials and documents according to Good Clinical Practice (GCP) and assist in the preparation of study documents for submission to the Ethics Committee and/or Phil FDA 
• Assists in the study-related meetings (GCP training; Site Initiation; Investigator's Meeting) , procurement of study equipment and supplies, and proper filing of all study-related documents 
• Documents clinical study team meetings and discussions with divisions 
• Tracks Clinical Research for on-going projects

Clinical Research Coordinator

<ul>
	<li>Communicates registration requirements to Enablers</li>
	<li>Handles Food and Drug Administration's registration documents</li>
	<li>Refers to the checklist needed to comply for submission</li>
	<li>Evaluates and assesses the completeness and correctness of documents</li>
	<li>Submits and monitors status updates of submitted documents</li>
	<li>Manages product registration and renewal of existing products</li>
	<li>Files Amendments/Variations with the Food and Drug Administration</li>
	<li>Prepares monthly operations reports and other assigned tasks</li>
</ul>

Regulatory Affairs Associate

Happy Skin is the country's favorite homegrown brand of makeup that cares for your skin. Made in the world's beauty capitals of Korea, Japan & Taiwan. ✨

PURPOSE:
Happy Skin was born to create and offer innovative products that are good for your skin. Each product should be of high quality, easy-to-use, approachable and non-intimidating, thus, empowering you with confidence & effortless beauty, and delivering happiness.

COMPANY VALUES:
1. Passion
2. Excellence
3. Innovation
4. Customer Happiness
5. Teamwork
6. Integrity
7. Work-Life Balance

Happy Skin

Job Description 
 
- Product management, development and innovations research 
- Project management 
- Coordination with suppliers 
- Managing product shipments 
- Coordinating shipment schedule with warehouse and marketing team 
- Application of IPO and FDA Requirements 
- Application of Importation Documents and Licenses

Assistant Innovations Manager

• Conducts sampling and inspection of Raw Material, Packaging Material or Imported Finished Bulk following standard operating procedures. Submits samples to QC Lab and/or QC Micro Lab for testing. 
• Evaluates supplier's certificate of analysis of delivered RM and IFB or certificate of inspection for PM. 
• Performs Raman ID Testing or Near-Infrared Region ID testing on delivered RMs per SOP. 
• Prepares Unilab Certificates of Analysis for raw materials.

Quality Control Analyst

OUR BUSINESS

First Gen Corporation (First Gen) is a leading independent power producer in the Philippines that primarily utilizes clean and indigenous fuels such as natural gas, geothermal energy from steam, hydro-electric, wind, and solar power. The company has 3,489 MW of installed capacity in its portfolio, powering 21.4% of the country’s gross generation.

First Gen is a natural gas pioneer and owns four out of the five natural gas-fired power plants in the country. These are the 1500-MW Sta. Rita and San Lorenzo plants, the 97-MW Avion and the 414-MW San Gabriel power plant. Avion will be the first power plant in the Philippines to run on aero-derivative gas turbines while the San Gabriel plant is expected to be the most efficient natural gas-fired plant in Southeast Asia. First Gen also has the largest portfolio of power plants that use clean, renewable and indigenous fuels. The plants are present in all three grids of the Philippines, and can serve the baseload, mid-merit and peaking market segments.

“Going forward, we continue to keep our eye on remaining relevant, effective, pioneering, and smart about the choices we make in moving towards a decarbonized world… First Gen continues to care about the world we live in, and we will continue to dare to make positive contributions.” 
– President and Chief Operating Officer, Francis Giles B. Puno

First Gen Corporation

Key Responsibilities:

<ul>
	<li>Regulatory and Industry Affairs- To monitor the regulatory side of the industry, give insights on different laws and policies concerning the company, and build networks to influence policy change and promote RE and the Company.</li>
	<li> </li>
	<li>Policy and Economic Analysis - To provide Power Economic information, forecasts, and analyses to support strategic planning of various internal and external stakeholders.</li>
	<li>Portfolio Management - To manage the Company’s portfolio through providing support, research, and analysis for Power Marketing, Trading, CSS, and Pi Energy, and through administering REM/RPS Compliance and the PREMS accounts of the Company’s facilities.</li>
</ul>

Qualification Requirements:

<ul>
	<li>Bachelor's degree in Economics, Engineering, Statistics or Mathematics</li>
	<li>Has skills in industry research, policy analysis, macroeconomic forecasting, and price modeling.</li>
</ul>

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Regulatory Affairs Specialist

Clinical Research Coordinator

Regulatory Affairs Associate

Assistant Innovations Manager

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Power Economics Analyst