Regulatory Affairs Manager

APL group; Cebu City; On-site; PHP 1,200,000 - 1,800,000; Full time

Job summary

Zuellig Pharma is recruiting a Regulatory Affairs Manager for its Sun Valley, Philippines operation. You will lead regulatory activities to ensure timely product registrations, lifecycle maintenance, and compliance for biologicals, vaccines, and healthcare products.

You will develop strategies to support market access and liaise with authorities and internal teams. The role requires a Pharmacy degree with licensure and 3–5 years of managerial regulatory experience, plus strong regulatory

Qualifications

• Bachelor's Degree in Pharmacy and licensed Pharmacist.
• 3–5 years of managerial Regulatory Affairs experience.
• Strong knowledge of pharmaceutical regulatory requirements and lifecycle management.
• Experience engaging with regulatory authorities and managing stakeholder relationships.

Responsibilities

• Prepare dossiers and submissions for biologicals, vaccines, and healthcare products.
• Ensure regulatory compliance across product lifecycle and support commercialization.
• Develop regulatory strategies and assess risks to approvals and market access.
• Collaborate with cross-functional teams and regional stakeholders.
• Represent the company before health authorities on regulatory matters.
• Review labeling, artworks, promotional materials, and Veeva submissions.
• Monitor regulations and provide regulatory intelligence to stakeholders.
• Maintain regulatory databases, trackers, and documentation.
• Support Regulatory Affairs Director with SOPs and process improvements.
• Represent the organization in industry associations and advocacy initiatives.

Skills

Regulatory leadership

Stakeholder management

Project management

Team leadership

Education

Bachelor's degree in Pharmacy

Tools

Veeva

Job description

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Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.

Regulatory Affairs Manager

Requisition ID: 2128

Posting Start Date: 26 Oct 2026

Location: Sun Valley, Philippines

Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.

The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.

Purpose of the Role:

The Regulatory Affairs Manager is responsible for leading regulatory activities to ensure timely product registrations, lifecycle maintenance, and compliance of biologicals, vaccines, and healthcare products. The role develops and executes regulatory strategies that support business objectives, ensures adherence to evolving regulatory requirements, and serves as the key liaison with regulatory authorities and internal stakeholders to facilitate product commercialization and market access.

What You'll Do:

• Evaluate and prepare dossiers and technical documents for new product registrations and submissions for biologicals, vaccines, and healthcare products.
• Ensure regulatory compliance of assigned products throughout the product lifecycle and support commercialization initiatives.
• Develop and implement regulatory strategies, identifying risks and opportunities that may impact product approvals and market access.
• Collaborate with partners, cross-functional teams, and regional stakeholders to communicate regulatory updates and drive regulatory objectives.
• Represent the company before regulatory health authorities, including FDA and other government agencies, on regulatory matters.
• Review and approve product labeling, packaging artworks, promotional materials, and Veeva submissions to ensure regulatory compliance.
• Monitor new and existing regulations, provide regulatory intelligence, and cascade regulatory updates to relevant stakeholders.
• Maintain regulatory databases, trackers, reports, and documentation to support compliance and business requirements.
• Support the Regulatory Affairs Director in strategy development, regulatory training, SOP creation, and process improvement initiatives.
• Represent the organization in industry associations and advocate for key regulatory and healthcare initiatives.

What Will Make You Successful:

Must-Have:

• Bachelor's Degree in Pharmacy and a licensed Pharmacist.
• At least 3-5 years of managerial experience in Regulatory Affairs.
• Strong knowledge of pharmaceutical regulatory requirements, product registration, and lifecycle management.
• Experience engaging with regulatory authorities and managing stakeholder relationships.

Advantage to Have:

• Experience handling biologicals, vaccines, and specialty healthcare products.
• Experience developing and executing regulatory strategies in a commercial environment.
• Familiarity with artwork, labeling, and promotional material review processes.
• Knowledge of Veeva and electronic document management systems.
• Experience in regulatory intelligence and policy monitoring.
• Strong project management and cross-functional collaboration skills.
• Experience developing SOPs and conducting regulatory training.
• Active participation in industry associations or regulatory advocacy initiatives.

What We Offer:

• We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
• We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
• As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
• Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
• Our Total Rewards program is designed to support your overall well-being in every aspect.

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Zuellig Pharma promotes an inclusive, fair workplace by ensuring equitable employment and compensation based on merit, regardless of background.