[Innovative Medicine] Associate Director, PV Systems and Vendor Management, Local Medical Safety, Japan

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Product Safety

Job Sub Function:

Pharmacovigilance

Job Category:

People Leader

All Job Posting Locations:

Chiyoda, Tokyo, Japan

Job Description:

Position Summary

The Associate Director, PV Systems and Vendor Management at Johnson & Johnson Innovative Medicine reports to the Country Safety Head, Local Medical Safety, Japan, and is responsible for leading the strategy, governance, and operational excellence of pharmacovigilance (PV) systems and vendor management.

This role ensures that PV systems and outsourced activities are compliant, efficient, and inspection and audit readiness, in alignment with global standards and Japanese regulatory requirements (e.g., PMDA, GVP).

The role is also responsible for budget and resource management for outsourcing, strategic outsourcing planning, and facilitating effective issue resolution between vendors and Local Medical Safety Japan.

Essential Job Duties and Responsibilities

1. Safety Systems Management

Lead governance and lifecycle management of PV systems in alignment with Global Medical Safety (e.g., safety database and related IT systems/tools)

Ensure compliance with global PV standards (GVP, GCP, Pharmaceuticals and Medical Devices Act, etc.)

Oversee system validation, upgrades, and change control processes

Collaborate with global teams for system harmonization and implementation of new tools

Drive data integrity and inspection readiness

Lead technical aspects of safety data migration or data transfer for MAH transfer projects.

2. Vendor Management

Manage vendors supporting pharmacovigilance operation activities

Lead selection, onboarding, and oversight of PV vendors (e.g., case processing, literature screening) in alignment with Global Medical Safety

Establish  and monitor KPIs, SLAs, and performance monitoring framework

Ensure vendor compliance with regulatory and quality standards

Manage escalation and issue resolution with vendors

Oversee outsourcing budget and resource planning aligned with business needs

Facilitate effective communication and issue resolution between vendor and Local Medical Safety Japan.

3. Operational Excellence & Compliance

Develop and optimize workflows to improve PV efficiency and quality in a technology aspect (e.g. AI and other technology tools in PV)

Ensure timely and compliant ICSR reporting to health authorities in a PV system (e.g., PMDA)

Support regulatory inspections and internal audits in a technical aspect (e.g., System verification of Database transfer)

Lead CAPA implementation related to systems or vendor quality issues

4. Leadership & Stakeholder Management

Lead and develop a team of system and vendor management professionals

Develop talents in the group, using mentor, coach and train and evaluate them

Assist the direct reports to exhibit their performance and provide opportunities for growth

Act as a key liaison with global PV, IT, QA, and external partners

Provide strategic input to LMS Japan Leadership Team

Drive cross-functional collaboration (e.g., Regulatory, Clinical, Medical)

Minimum Qualification Required

Bachelor, Masteror other equivalent advanced degree in a biological or medically related field is required.

Minimum 5–8 years of experience in Pharmacovigilance, with a minimum of 2 years in case management desired

Minimum of 3 years of direct team management.

Strong experience in PV systems (e.g., Argus, ArisG, LSMV) and vendor management is desired

In-depth knowledge of PV regulations (GVP, GCP, ICH guidelines, Pharmaceuticals and Medical Devices Act) Experience in regulatory inspections and audits

Highly effective written, oral, and interpersonal communication skills in Japanese and Business-level English is required.

Demonstrated ability to think strategically, lead through change and build teams.

Preferred

Experience in global/matrix organization

Project management experience (system implementation or transformation)

Knowledge of digital/automation tools (e.g., RPA, AI in PV)

Vendor outsourcing/transition experience

Knowledge of ICSR management

＜For Internal Applicants＞

Based on your experience and interview evaluation, the position title and level may vary.

If you are Japan employee, please read “Internal Application Guideline” in Ask GS. Especially if you are less than 18 months in your current role, you are required to obtain application approval from your current manager as well as your respective BUHR. If you are Japan’s employee, you are not able to apply for multiple positions at once.

For Employee Referral Program (ERP), please read and understand the details of the “Internal Referral Overview” on the Ask GS and you have made a compliant referral.

Required Skills:

Preferred Skills:

Developing Others, Global Market, Inclusive Leadership, Leadership, Medicines and Device Development and Regulation, Operations Management, Performance Measurement, Pharmacovigilance, Quality Control (QC), Quality Management Systems (QMS), Regulatory Affairs Management, Report Writing, Safety Investigations, Safety-Oriented, Safety Reporting, Serious Adverse Event Reporting, Team Management