[Singapore] Global Safety Vigilance Risk Management Lead at Santen

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

27 Sep, 26

Salary

0.0

Posted On

29 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Risk Management, Signal Assessment, Regulatory Affairs, Clinical Development, NDA/MAA Dossier Preparation, Aggregate Safety Reporting, PSUR, DSUR, Strategic Thinking, Cross-functional Leadership, English Communication, MS Office, Medical Affairs, Patient Safety, Ophthalmology

Industry

Pharmaceutical Manufacturing

Description

Company Description Santen is a specialized company with a proud 130-year heritage focused exclusively on eye health. As a Japan-originated, global company with our footprint in over 60 countries and regions, our mission is to provide essential and significant value to patients and society through our products and services created from our expertise in ophthalmology and from the patient’s perspective. Due to significant expansion, Santen Pharmaceutical is seeking a Global Safety Vigilance Risk Management Lead. Based in Singapore, the incumbent is responsible for spearheading the end-to-end strategy, execution, and maintenance of safety vigilance activities across Santen’s global portfolio. This includes ensuring the highest standards of quality and consistency for medicinal products, medical devices, and supplements throughout both the clinical development and commercial lifecycles. By establishing robust global risk management structures and operational frameworks, the Lead ensures full alignment with international regulatory standards and internal policies. Job Description What you will do 1. Considering impact on subject/patient safety and product value maximization from development to post-marketing stage. 2. Flexible mindset and refined negotiation skill to achieve challenging targets. 3. Act as Product Safety Lead with responsibility for risk management activities as below for Santen investigational and post-marketing products. Preparation of signal assessment documents Creation of action plans to mitigate/manage product risks Development and maintenance of product Core Risk Management Plans (cRMP) and Company Core Safety Information (CCSI) Preparation of aggregate safety report such as PSUR Development of clinical trial relevant documents such as DSUR, safety management plan, periodic risk monitoring of investigational products Leading preparation for safety relevant documents for NDA/MAA dossier in collaboration with other SV members and relevant stakeholders with deep understanding for requirements and requests in the applied country as well as submitted dossier and communication with the health authorities in other regions/countries referenced by the applied country. Contribute to R&D project as a representative of SV with scientific and strategic input 4. In addition, provides support to SV related activities/projects globally according to the direction made by head of Medical Evaluation and Risk management at any given time. Qualifications What you will bring to the role Experience in drug safety activities but not limited in PV function in pharmaceutical companies (e.g. pharmacovigilance, medical affairs, medical science liaison, regulatory affairs, R&D, clinical development, non-clinical research, etc.) for more than 5 years. Bachelor’s degree in Life Science or a related field, preferably pharmacist. High compatibility with scientific and strategic way of thinking to find solution even in complicated situations. Experience in cross functional and regional projects (e.g. R&D project). Experience in risk management for medicinal product. Knowledge of products development process including preparation for NDA/MAA dossier. Familiarity with and ability to work as a stand-alone or a few members of Pharmacovigilance unit within a global Safety Vigilance Structure Well-organized and detail oriented, with strong verbal and written communication skills in English Ability to effectively participate in multi-disciplinary teams; strong hands-on leadership Solid decision-making skills, inter-dependent partnering skills, team-orientation and demonstrated ability to influence outcomes. Solid computer skills, using MS Office / Word. Additional Information Grow your career at Santen A career at Santen is an opportunity to make a difference. We aspire to contribute to the realization of “Happiness with Vision” by providing eye health products and services to patients, consumers, and medical professionals around the world. Guided by our CORE PRINCIPLE, “Tenki ni sanyo suru”, Santen is engaged in the global research & development, manufacturing, and sales and marketing of pharmaceutical products in opthlamology. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes, education and treatment. At Santen, we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment. The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs, role requirements and individual qualifications regardless of race, color, ethnicity, national origin/ancestry, religion, sexual orientation, gender, gender identity/ expression, age, disability, medical condition, marital status, veteran status, or any other characteristic protected by law. If you require any kind of accommodation during our recruitment process, please let the recruiter from our team know.

Responsibilities

Lead the end-to-end strategy and execution of global safety vigilance and risk management activities for medicinal products and medical devices. Responsible for creating risk mitigation plans, maintaining core safety information, and preparing aggregate safety reports for regulatory submission.