Life Sciences Job at Zuellig Pharma, Thailand | Pharmacovigilance Associate | Apply Now
If you are a pharmacy, medicine, or life sciences graduate looking to combine drug safety operations with specialized medical communication, this full-time role at Zuellig Pharma is an exceptional opportunity. Located within Zuellig Pharma’s extensive commercial network in Thailand, this position places you on the front lines of drug safety and market-entry compliance in Asia. For early-to-mid career professionals searching for a high-impact Life Sciences Job, this role offers a diverse dual scope: executing core Individual Case Safety Report (ICSR) processing alongside managing critical medical information queries. It serves as an elite corporate milestone for a long-term Pharmacovigilance Associate Job and stands out as a premier choices for anyone tracking a competitive, compliance-driven Job in Thailand within a multi-billion-dollar healthcare solutions matrix.
- Job Position: Pharmacovigilance Associate
- Requisition ID:Â 1709
- Location: Thailand
About The Company
Zuellig Pharma is a leading regional healthcare solutions powerhouse in Asia, driven by a century-long purpose to make healthcare fully accessible to the communities it serves. Boasting a multi-billion-dollar footprint covering 17 markets and employing over 12,000 personnel, the company distributes advanced therapeutics, digital platforms, and commercial solutions to more than 200,000 medical facilities.
Zuellig Pharma partners directly with over 450 global clients, including the top 20 pharmaceutical corporations in the world. Operating under strict international quality standards (including GDSP, GMP, and ISO 9001), the localized pharmacovigilance and medical affairs business units function as essential compliance gates—ensuring that side-effect profiles and product tracking models satisfy both strict internal parameters and the specific requirements of the Thailand Food and Drug Administration (Thai FDA).
Life Sciences Job – Key Responsibilities
This role uniquely balances high-compliance drug safety tracking with a client-facing medical communications desk, splitting your daily priorities across two essential functional areas:
- Pharmacovigilance Operations (50% – 70% of Scope)
- Adverse Event Lifecycle Management: Managing and maintaining active involvement in daily Adverse Event (AE) reporting, tracking active cases, and executing detailed case follow-ups.
- ICSR Governance & Submissions: Collecting, handling, and submitting Individual Case Safety Reports (ICSRs) associated with in-licensed products to relevant principals and regulatory authorities within mandatory legal windows to advance this Life Sciences Job.
- Localized Literature Review: Conducting regular, systematic screenings of domestic medical journals and scientific literature to extract, evaluate, and log hidden or unlisted adverse reactions.
- Aggregate Reporting Collaboration: Partnering with the internal Regulatory Affairs department to prepare, compile, and submit Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs), and Periodic Benefit-Risk Evaluation Reports (PBRERs).
- Data Reconciliation & Audits: Executing routine monthly safety reconciliations across cross-functional internal units, while supporting both internal quality reviews and external global client PV audits or health authority inspections to support this Pharmacovigilance Associate Job.
- Medical Information Responsibility (30% – 50% of Scope)
- HCP Query Management: Handling direct inquiries from Healthcare Professionals (HCPs) and consumers, providing highly accurate, balanced, and non-promotional product metrics.
- Safety & Complaint Triaging: Identifying and flagging inbound queries that contain either potential adverse events or product quality complaints (PQCs), routing them immediately into appropriate cGCP/SOP tracking lanes.
- Good Documentation Practices (GDP): Recording clinical and pharmaceutical communication transactions into specialized corporate databases, ensuring all text entries are concise, thorough, and auditable.
- Enquiry Escalation: Utilizing predefined knowledge databases to fulfill standard customer requests, while escalating novel or complex medical questions to global principal partners.
Qualifications & Profile Requirements For Life Sciences Job
Zuellig Pharma seeks a balanced, analytical life scientist who can navigate localized corporate databases efficiently and resolve routine tracking friction constructively under minimal supervision.
- Required Academic Baseline:
- Educational Foundation: A formal university Degree or Advanced Degree in relevant Life Sciences discipline required for a premium Job in Thailand.
- Desirable Experience & Competencies:
- Practical experience or operational exposure navigating pharmacovigilance tracking workflows, safety data collection methods, or medical call center databases.
- Proven ability to solve routine problems, make informed choices with an acute understanding of compliance consequences, and hit individual performance benchmarks.
- A deep commitment to clinical data integrity, patient privacy rules, ethical standards, and precise medical documentation habits.
- Strong communication and interpersonal traits to work effectively with matrixed internal departments, external commercial stakeholders, and international manufacturing principals.
In short, the Pharmacovigilance Associate position at Zuellig Pharma is a definitive route to transitioning your scientific or pharmaceutical background into a highly valuable regional commercial asset. Securing this appointment allows you to move past generalized bench support and take active, dual command of the case safety datasets, literature reviews, and medical communications platforms that maximize drug safety across Southeast Asia. If you reside in Thailand, hold a qualifying life sciences degree, and possess basic exposure to PV guidelines, apply today to secure this premier Life Sciences Job, launch a highly rewarding Pharmacovigilance Associate Job, and lock in this outstanding Job in Thailand.
