Pharmacovigilance Job at Celltrion | Apply Now
Pharmacovigilance job opportunities are rapidly growing in the global healthcare and life sciences industry, offering exciting roles for fresh graduates and early-career professionals. This latest opening at Celltrion Inc provides a strong foundation for those looking to build a career in drug safety, regulatory compliance, and patient-focused healthcare solutions. If you are seeking a life science job with global exposure and impactful work, this opportunity is worth exploring.
- Job Position: Pharmacovigilance Associate
- Location: Taguig, National Capital Region, Philippines
About the Company
Pharmacovigilance job opportunities at Celltrion Inc offer candidates a chance to work with a globally recognized biopharmaceutical company known for innovation in biosimilars and biologics. Celltrion careers are highly valued in the life science job market due to the company’s commitment to improving patient access to advanced therapies and maintaining strong regulatory standards worldwide.
Job Description
Pharmacovigilance job responsibilities include supporting drug safety operations through the review, processing, and assessment of adverse event reports. This life science job ensures accurate data handling, timely case processing, and compliance with global pharmacovigilance standards while contributing to patient safety and regulatory obligations.
Qualifications
- Pharmacovigilance job requirements include a Bachelor’s degree in Life Sciences, or related healthcare discipline
- Fresh graduates or candidates with up to 2 years of relevant experience are welcome to apply
- Experience in pharmacovigilance, healthcare, clinical, retail pharmacy, or research is an advantage
- Strong English communication skills, both written and verbal
- Excellent attention to detail, organization, and time management skills
- Ability to work independently and in a fast-paced environment
- Proficiency in MS Office and familiarity with databases/safety systems is a plus
- Strong teamwork skills with the ability to work in multicultural environments
Key Responsibilities
- Pharmacovigilance job duties involve reviewing and processing adverse event and product safety reports within required timelines
- Perform accurate case data entry, coding, and duplicate checks in safety databases
- Draft concise and medically accurate case narratives and follow-up queries
- Conduct initial case assessments based on established procedures and guidelines
- Maintain documentation, trackers, and quality records related to case processing
- Ensure compliance with internal SOPs, quality standards, and regulatory requirements
- Collaborate with internal stakeholders to support workflow continuity and team objectives
- Participate in training, process improvement, and cross-functional initiatives
