Manager, Quality Systems
Job in
Princeton, Mercer County, New Jersey, 08543, USA
Listed on 2026-01-26
Listing for:
Otsuka Pharmaceutical Co., Ltd
Full Time
position Listed on 2026-01-26
Job specializations:
-
Healthcare
Job Description & How to Apply Below
** Inspections, CAPA, Change Control, Document Management, and Training**. The ideal candidate will serve as a strategic partner to IT, enabling digital transformation and governance across the global quality landscape.
** Key Responsibilities
*** Quality Systems Management:
Lead the development, deployment, and governance of core quality systems (e.g., CAPA, Change Control, Deviation Management, Document Management, Training, Audit Management). Serve as the
** business process owner
** for quality system platforms, ensuring alignment with business needs and regulatory expectations. Lead or support
** global projects
** related to system implementation, validation, and lifecycle management.
* Process Optimization:
Identify and implement process improvements to enhance efficiency, compliance, and user experience across quality systems. Drive
** process harmonization and standardization
** across global sites to ensure compliance with regulatory requirements (e.g., FDA, EMA, ICH, ISO).
* Digital Transformation:
Partner with IT to define and implement
** digital solutions**, system upgrades, and enhancements that improve usability, efficiency, and data integrity.
* Governance:
Develop and maintain
** governance frameworks**, including metrics, dashboards, and KPIs to monitor system performance and compliance.
* Training & Change Management:
Support training initiatives and change management efforts to support global adoption of quality systems and processes.
* Stakeholder Engagement:
Collaborate with cross-functional teams including Regulatory Affairs, Manufacturing, R&D, and Supply Chain to ensure alignment and integration of quality systems.
** Qualifications
* * Required
*
* Required Qualifications:
*** Bachelor’s degree in Life Sciences, Engineering, Pharmacy, or related field (Master’s preferred).
* Experience:
* 6+ years of experience in pharmaceutical quality, quality systems, or compliance.
* Proven experience implementing and managing global quality systems in a regulated environment.
* Experience with eQMS platforms (e.g., Veeva, Track Wise, Compliance Wire).
* Skills &
Competencies:
* Strong knowledge of GxP, ICH guidelines, and global regulatory requirements.
* Excellent project management, analytical, and communication skills.
* Ability to lead cross-functional initiatives and influence without authority.
* Familiarity with Lean, Six Sigma, or other continuous improvement methodologies.
* Preferred Experience:
* Experience in global or matrixed organizations
* Knowledge of risk management frameworks (e.g., ICH Q9)
* Experience supporting regulatory inspections and audits Preferred
* Experience in pharmaceuticals/medical devices or other regulated industry
* Embody a customer service mentality as you communicate and support field sales teams
* Experience leading Contract Workers remotely
** 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 $ - Maximum $, plus incentive opportunity:
The range shown represents a typical pay range or starting pay for individuals…
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