Regulatory Affairs Specialist
A leading global animal health organisation is seeking a Regulatory Affairs Specialist to join their team in Taguig. This is an exceptional opportunity for you to play a pivotal role in ensuring that the company’s innovative products and services consistently meet local regulatory and quality standards, enabling safe and efficient operations.
What you'll do:
As a Regulatory Affairs Specialist based in Taguig, you will immerse yourself in a multifaceted role that bridges regulatory affairs, marketing support, technical services assistance, and quality assurance.
- Maintain professional relationships with government regulatory agencies to ensure seamless communication and compliance with all relevant regulations.
- Secure necessary documents for product registration processes such as line extensions, reformulations, new sourcing initiatives, and shelf-life extensions.
- Organise and maintain comprehensive regulatory documentation systems that support efficient retrieval and audit readiness at all times.
- Obtain and renew essential licenses, product registrations, and permits required for importation, distribution, trading, and exportation activities.
- Ensure timely submission of applications to achieve compliant product approvals within established deadlines.
- Liaise regularly with regulatory authorities to stay updated on evolving requirements and represent the department in both local and global project teams.
- Coordinate the review of product literature, labels, and packaging components to guarantee alignment with current regulatory standards.
- Collaborate on pharmacovigilance reporting by providing feedback on safety data and supporting related documentation needs.
- Manage the documentation process for change notifications while ensuring proper closure according to internal procedures.
- Prepare product artwork—including labels, inserts, and packaging—in strict compliance with applicable regulatory requirements.
What you bring:
The ideal Regulatory Affairs Specialist brings proven experience from roles within the pharmaceutical or veterinary sectors where they have developed a deep understanding of local regulations governing product registration, licensing processes, import/export requirements, pharmacovigilance practices, dossier evaluation procedures before release of goods into market channels—and more.
- A bachelor’s degree or higher qualification in Veterinary Medicine, Pharmacy, or another paramedical field provides the foundational knowledge required for this role.
- At least 2–4 years of experience working in regulatory affairs or quality assurance within the pharmaceutical or veterinary industry ensures familiarity with industry-specific challenges.
- Active involvement in industry or regulatory associations is considered an advantage as it demonstrates engagement with broader professional networks.
- Excellent interpersonal skills enable effective collaboration with internal teams as well as external stakeholders such as government agencies.
- Clear written and verbal communication abilities are essential for preparing documentation and liaising with authorities.
- A keen eye for detail supports accurate record-keeping and ensures compliance across all aspects of regulatory submissions.
- Proficiency in computer applications facilitates efficient management of documentation systems and reporting tasks.
- Demonstrated problem-solving skills allow you to address issues proactively while maintaining high standards of quality.
- A commitment to ongoing education reflects your dedication to personal development within the field of regulatory affairs.
What sets this company apart:
This organisation stands out as a global leader dedicated exclusively to advancing animal health through cutting-edge medicines, vaccines, diagnostics solutions & genetic testing services tailored specifically for pets/livestock alike.
What's next:
If you are ready to take your expertise in regulatory affairs to the next level within a globally respected animal health organisation—this is your chance!
Apply today by clicking on the link provided—your future as a valued Regulatory Affairs Specialist awaits!
Due to the high volume of applications we are experiencing, our team will only be in touch with you if your application is shortlisted.
About the job
Contract Type: Perm
Specialism: Industrial
Focus: Operations
Industry: Pharmaceuticals
Salary: Negotiable
Workplace Type: On-site
Experience Level: Mid Management
Location: Taguig
FULL_TIMEJob Reference: SE4WYQ-F6C04D75
Date posted: 6 November 2025
Consultant: Athena Samson
philippines industrial/operations 2025-11-06 2026-01-05 pharmaceuticals Taguig National Capital Region PH Robert Walters https://www.robertwalters.com.ph https://www.robertwalters.com.ph/content/dam/robert-walters/global/images/logos/web-logos/square-logo.png true