PV Medical Manager – Deputy QPPV at ZOETIS SINGAPORE PTE LTD

Zaventem, Flanders, Belgium -

Full Time

Start Date

Immediate

Expiry Date

15 Feb, 26

Salary

0.0

Posted On

17 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacovigilance, Signal Management, Regulatory Compliance, Data Analysis, Veterinary Medicine, Interpersonal Skills, Database Software, Epidemiology, Risk Mitigation, Adverse Drug Experience Reporting, Trending Reports, Collaboration, Negotiation, Policy Design, Subject Matter Expertise

Industry

Pharmaceutical Manufacturing

Description

The EU Pharmacovigilance Medical Manager/Deputy QPPV is a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE submissions to CVM, pharmacovigilance SOPs, and Signal Management responsibilities. Duties and Responsibilities include but not limited to: Good understanding of the ADE reporting regulations (US and EU) and of product trending standards. Collaborate with signal management team regarding validation activities for assigned products (including signal detection) to comply with FDA/USDA/EU expectations and to better understand the safety and efficacy profiles of Zoetis products post-marketing. Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders and make recommendations regarding potential safety and efficacy profile adjustments. Provide input for negotiations with regulatory agencies regarding submission of ADE reports as well as for responses to these agencies about product safety and efficacy issues. Assist in the design pharmacovigilance policies as needed. Assist in the maintenance of a pharmacovigilance electronic system from a data capture, trend analysis and regulatory submission perspective as necessary. Function as Pharmacovigilance subject matter expert for assigned product group(s). Provide pharmacovigilance input for advertising and promotional material upon request. Risk Mitigation in support of Global Manufacturing and Quality and Regulatory label defense activities. Complete PV Data requests and Health Hazard Assessments for assigned products upon request. Act as Deputy EU/UK QPPV Minimum requirement of a Veterinary Medicine (DVM, VMD) and 5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the European Union. Additional graduate degree or diploma in animal science and/or epidemiology or related experience is a plus. Ability to review and analyze pharmacovigilance data to develop trending reports is essential. Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting is a benefit. Strong interpersonal skills, ability to work under pressure and in a highly matrix environment is essential. Experience with database software and pharmacovigilance systems is desirable. May lead/mentor others Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses. Why Zoetis Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers. Zoetis work environment At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow. Your opportunities at Zoetis We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health. Results that matter Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face.

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Responsibilities

The role involves contributing to global pharmacovigilance activities, including ADE reporting and signal management. The Deputy QPPV will prepare trending reports and provide input for regulatory negotiations regarding product safety and efficacy.