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
To support Regulatory Affairs and Distribution Operations functions while undergoing the Provisional Registered Pharmacist (PRP) training program. The role provides hands-on exposure to product registration, regulatory compliance, and distribution activities under the supervision of a fully registered pharmacist, ensuring readiness for full professional registration.
What You'll Do
- Support preparation and submission of regulatory applications (e.g., new registrations, variations, renewals) in accordance with NPRA requirements.
- Assist in compiling and verifying regulatory documents to ensure completeness and compliance prior to submission.
- Support maintenance of regulatory trackers, databases, and documentation in line with internal processes and audit requirements.
- Liaise with internal stakeholders to follow up on required documents and information for submissions.
- Provide support in responding to regulatory authority queries under supervision.
- Assist in distribution-related regulatory activities, including permit applications, documentation, and compliance checks.
- Support implementation of Good Distribution Practice (GDP) requirements within the organization.
- Participate in pharmacovigilance (PV) and regulatory compliance activities, where applicable.
- Attend training sessions and actively participate in structured PRP development programs.
- Perform other duties as assigned to support Regulatory Affairs and Distribution Operations.
What Will Make You Successful
- Strong willingness to learn and adapt in a structured training environment.
- High level of responsibility and attention to detail when handling regulatory documents.
- Good time management and ability to follow through on assigned tasks.
- Effective communication and collaboration with team members.
- Positive attitude, discipline, and commitment to professional development.
Must-Have
- Bachelor's Degree in Pharmacy and eligible for Provisional Registration with Malaysian Pharmacy Board.
- Strong interest in Regulatory Affairs and/or Pharmaceutical Distribution.
- Good written and verbal communication skills in English.
- Proficient in Microsoft Office applications (e.g., Excel, Word, PowerPoint).
Advantage To Have
- Internship or industrial training experience in pharmaceutical industry.
- Exposure to regulatory affairs, quality assurance, or distribution operations.
- Basic understanding of NPRA requirements and pharmaceutical regulations.
- Familiarity with Good Distribution Practice (GDP).
- Strong organizational and documentation skills.
- Ability to work independently with guidance.
- Attention to detail and accuracy in data handling.
- Positive learning mindset and proactive attitude.
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.
