Johnson & Johnson Careers

[Janssen] Medical Safety Specialist

Taipei, Taiwan
Drug & Product Safety Operations


Job Description

Requisition ID: 1905750355W

Description

 

A global leader in health and personal care, with over 125,000 employees in over 275 companies in 60 countries. We work with partners in healthcare to touch the lives of more than a billion people every day throughout the world. Johnson & Johnson companies market leading products and services in three business segments: Consumer, Pharmaceuticals, and Medical Devices.

“By caring, one person at a time, we aspire to help billions of people live longer, healthier, happier lives.”

We have a new and exciting opportunity to hire a Medical Safety Specialist for our Pharmacovigilance here at Taipei, Taiwan office.


 

Job Purpose and Scope:

Support the Medical Safety – Associate Manager to fulfil the responsibility for the coordination and execution of all Medical Safety (MS) activities across the Pharmaceutical and Consumer sectors. Act as one of the Local Operating Company (LOC)’s and assigned territories’ (as applicable) contact point for Medical Safety matters with Global Medical Organisation (GMO), Office of Consumer Medical Safety (OCMS), Global Medical Safety (GMS). Support PV team and LOC stakeholders to meet all global and local MS responsibilities.

 


Core Job Responsibilities:

Medical Safety Specialist - Taiwan:

Support the oversight of MS activities –

               Support oversight of the assigned cross sector product portfolio, and link with local management and key stakeholders

               Support to maintain oversight of all required MS regulatory reporting compliance in a timely manner e.g RMPs, aggregate reports.

               Advise the business on the MS impact of local organized data collection programs, post marketing programs, RWE studies etc.

               Escalate compliance issues in a timely manner to Line Manager and North Asia Cross Sector Safety Area Lead to ensure appropriate mitigation is implemented.

               Monitor and forecast MS workload to identify, mitigate and escalate potential MS resource and non-compliance issues.

         Support and lead process improvements to optimize MS activities.

         Work collaboratively with regional affiliates to ensure consistency of approach across groups.

         Build and maintain effective business relationships across the LOC.

         Provide high quality and consistent input to development of local safety initiatives and programs.

               Support the maintenance of  an environment of continuous improvement within the MS team and contribute to continuous improvement initiatives across the region and globally with GMO, OCMS and GMS.


Key Medical Safety Activities:

               Support signal detection – ensure LOC complies with any local HA signal-detection requirements, collaborate with regional and global colleagues to signal detection activities and communications.

               Support intensive monitoring programs including Compassionate Use Program, Patient Access Program, Registries, Post-Marketing Studies – involvement with key stakeholders to ensure the programs meet local, regional or global requirements from a compliance and strategic safety perspective.

               Monitor any MS service providers to ensure PV and MS obligations are being fulfilled.

 

Risk Management:

               Have an appropriate system of and Risk Management in place in order to assure appropriate oversight for products within its responsibility

         Review and complete country specific Annex as required according to local requirements, if applicable

               Collaborate with Medical Affairs and Regulatory Affairs team to ensure that RMP activities are completed on a timely manner

               Ensure implementation and tracking of RMP activities are in place including documentation of completed activities

         Review all risk management plans and PSURs to obtain information on the risk/benefit profile of products

               Monitor the risk/benefit profile of local products and communicate changes or safety issue/concerns to the APAC Cross Sector Safety Team Lead, and the QPPV (for products marketed in the EMEA) for evaluation.

•               Provide MS input in pre-authorisation phase/submission-planning phase of product lifecycle to guide appropriate planning and management of RMP-related activities.



Qualifications

Experience, Skills and Knowledge:

·         2 years of experience in PV/Medical safety related field essential; experience working in the pharmaceutical industry is strongly preferred

·         Experience in conducting training

·         Knowledge of PV regulations

·         Experience using global safety database desirable

·         Demonstrated attention to detail

·         Excellent written and spoken communication and presentation skills

·         Effective decision maker with the ability to assess impact of actions taken locally on the global PV system

·         Fluency in written and oral English in order to facilitate communications with GMO, regional Medical, other global functions, and Health Authority

·         High customer orientation

·         Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity

·         Sound judgment, strong planning and organizational skills, and the ability to get things done

·         Demonstrated strong sense of urgency

·         Strong influencing skills with the ability to explain and defend a position which is in the best interests of patient safety



Primary Location
Taiwan-Taipei-Taipei-
Organization
Johnson & Johnson Taiwan, Ltd. (8580)
Job Function
Drug & Product Safety Operations
Requisition ID
1905750355W