Otsuka Pharmaceutical Companies (U.S.)

Associate Director, GPV Compliance & Business Management

Otsuka Pharmaceutical Companies (U.S.)  •  $150k - $224k/yr  •  Princeton, FL (Onsite)  •  2 hours ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

The Compliance & Business Management (CBM) team supports key Pharmacovigilance (PV) operational, compliance, and business activities across the organization. This role ensures PV compliance, supports contract management, facilitates audit and inspection readiness, manages CAPA and deviation processes, and contributes to metrics reporting, alliance management, training, SOP governance, and documentation quality.

Responsibilities within the CBM team are interchangeable and may shift based on business needs or direction from leadership.

The Associate Director, GPV Compliance & Business Management, supports the development, implementation, and continuous improvement of GPV compliance systems to ensure alignment with global regulatory requirements and internal quality standards. This role leads assigned CBM areas and may coordinate operational activities of vendor partners to maintain strong compliance processes.


Key responsibilities include:
• Operational Leadership: Lead assigned CBM functional areas and contribute to broader compliance strategy development in collaboration with Global Quality and internal GPV stakeholders.
• Cross-Functional Collaboration: Work proactively with affiliates, other Otsuka companies, and internal partners to ensure aligned and compliant practices.
• Internal Coordination: Partner with CBM leads to ensure consistent execution across sub-functions.
• Vendor Oversight: Provide oversight of vendor activities within assigned domains.

This role may be responsible for managing direct reports.

KEY RESPONSIBILITIES

GPV Due Diligence and Alliance Management

  • Supports the lifecycle relationship with collaborating companies through PV due diligence activities, development and maintenance of Pharmacovigilance Agreements (PVAs), and ongoing compliance oversight.
  • Works cross‑functionally across GPV and with internal Otsuka stakeholders to build alignment, promote mutual understanding, and ensure GPVAM processes are integrated appropriately within Global Pharmacovigilance.
  • Partners with GPV and cross‑functional leaders to contribute to strategies that support effective and compliant alliance management.
  • Contributes to the harmonization and integration of affiliate companies into GPV processes across functions and regions.
  • Manages day‑to‑day GPV alliance activities across Otsuka companies and partners, including preparation, coordination, and facilitation of Pharmacovigilance Committee (PVC) meetings.
  • Develops and applies best practices to enhance efficiency and consistency in partner relationship management processes.
  • Ensures adherence to global, local, and regional PV requirements and internal policies/procedures, and supports corrective and preventive actions related to PVAs when needed.
  • Identifies opportunities to support globalization of GPV processes across functional areas, regions, and affiliates through enhanced collaboration and alignment.
  • Facilitates cross‑functional and partner‑related issue resolution by coordinating discussions, clarifying responsibilities, and ensuring timely follow‑through.
  • Oversees assigned team members to support compliance with applicable PV requirements, internal standards, and organizational processes.
  • Provides guidance, training, and support to direct reports and GPV colleagues on integration and alliance‑related activities.
  • Serves as a point of contact for GPVAM for assigned alliances during audits and regulatory inspections, supporting evidence gathering and responses.
  • Leads the PV component of CBM due diligence processes for assigned BD projects, focusing on assessment of the target company’s PV capabilities.
  • Submits questions through Letters of Query (LoQ), reviews responses, and assesses implications for PV processes and compliance.
  • Reviews relevant materials in data rooms and shared repositories to evaluate PV systems, organizational structure, and potential risks.
  • Identifies and synthesizes key risks, organizational gaps, and challenges and escalates them to PV leadership as appropriate.
  • Contributes to the preparation of structured due diligence reports, ensuring findings are well documented, clearly articulated, and aligned with PV leadership expectations.
  • Supports presentation of PV due diligence outcomes and recommendations to the Business Development (BD) team and other stakeholders.

Additional activities:

  • Attend Global / Regional meetings as required
  • Present compliance metrics at Global Meetings
  • Contribute to maintenance of PV System Master File as required.
  • May be assigned to lead or assist with special projects or process development.
  • Collaborate with the Regional PV offices for process improvement initiatives and corrective and preventive actions identified by the Regional PV offices
  • May perform any other duties as needed.

JOB SCOPE (key facts & figures)

  • Travel as applicable
  • Knowledge of ICH, US & EU regulations and requirements for pharmacovigilance
  • Solid background and experience in pharmaceutical quality system management (GxP)
  • Experience with coordination and/or participation in PV audits in the pharmaceutical industry
  • Strong project management, interpersonal, communication and presentation skills
  • Ability to accomplish objectives through influence in a matrix organization
  • Strong computer skills with Word, Excel, PowerPoint, and Outlook

QUALIFICATIONS/ EXPERIENCE REQUIRED

  • Bachelor's degree- required
  • Experience working in a global setting
  • Experience in managing vendor relationships and oversight
  • Minimum 4 years PV Compliance or Quality Management experience in the pharmaceutical industry or relevant leadership experience
  • Microsoft proficient- Essential
  • Knowledge of ICH, US & EU regulations and requirements for pharmacovigilance
  • Solid background and experience in pharmaceutical quality system management (GxP)
  • Experience with coordination and/or participation in PV audits in the pharmaceutical industry

COMPETENCIES REQUIRED

  • Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
  • Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
  • Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
  • Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
  • Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
  • Empowered Development - Play an active role in professional development as a business imperative.

Competencies
Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
Empowered Development - Play an active role in professional development as a business imperative.

Minimum $150,034.00 - Maximum $224,250.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline This will be posted for a minimum of 5 business days.

Company benefits: Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

Come discover more about Otsuka and our benefit offerings; https://www.otsuka-us.com/careers-join-otsuka

Disclaimer:

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Otsuka is an equal opportunity employerAll qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disabilityYou can request reasonable accommodations by contacting Accommodation Request

Statement Regarding Job Recruiting Fraud Scams

At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.

Please understand, Otsuka will never ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.

Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.

To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External

Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka’s call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov, or your local authorities.

Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. (“Otsuka”) does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka’s application portal without a valid written search agreement in place for the position will be considered Otsuka’s sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Otsuka Pharmaceutical Companies (U.S.)

About Otsuka Pharmaceutical Companies (U.S.)

There are two Otsuka pharmaceutical industry companies in the U.S.:

Otsuka America Pharmaceutical, Inc. (OAPI) successfully commercializes Otsuka-discovered and in-licensed products in North America.

Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) clinically develops and registers innovative healthcare products on a global basis.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Princeton, NJ
Year Founded
Unknown
Social Media