drjobs NV_Quality Assurance Manager_Beijing

NV_Quality Assurance Manager_Beijing

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1 Vacancy
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Job Location drjobs

Beijing - China

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Flexibility: Hybrid

Position summary:

Lead the China NV QA team to build and maintain a compliant effective and inspection-ready Quality Management System that safeguards patient safety and supports NV business growth. Ensure every product released in China meets China regulations and Stryker requirements.

Essential Duties & Responsibilities: (Detailed Description)

  • Develop annual QA strategy budget and resource plan aligned with business needs and NMPA focus areas.

  • Build defend and continuously improve a best-in-class Quality Management System covering the full product life-cycle.

  • Build and mentor a high-performing team capable of hosting unannounced NMPA inspections at both local and overseas sites.

  • Lead the NV team to pass both domestic and overseas NMPA inspections with minimal business disruption.

  • Establish proactive post-market surveillance programs for NV products especially for VBP products; drive trending and risk-benefit reassessments.

  • Review analyze and report quality discrepancies; author dispositions and corrective actions for recurring issues.

  • Support Operations and third-party warehouse management to ensure compliant product distribution and sales.

  • Serve as primary interface with NMPA provincial bureaus and global QA/RA functions; maintain credibility and rapid escalation paths.

  • Anticipate regulatory changes (e.g. random inspection for VBP products overseas facility audits) and implement preventive actions before mandates take effect.

  • Plan execute and monitor the QA team objectives; track KPI closure rates.

  • Own the local QA budget.

  • Complete other assignments as directed by senior management.

Education & Experience:

  • Bachelors degree or above in Biomedical Engineering Pharmacy Mechanical Engineering or related field.

  • 8 years of progressive QA experience in interventional/implantable medical devices including 3 years leading teams.

  • In-depth knowledge of NMPA regulation such as ISO 13485 GMP.

  • Proven track record of successfully hosting NMPA targeted or unannounced inspections.

  • Fluent English (written & spoken) for global collaboration.

Physical & Mental Requirements:

  • Well-organized and logical thinking

  • Good at strategy making

  • Detailed oriented

  • Professional communication skills

  • Team player

  • Patience and a great sense of responsibility

Leadership (People Management requirement)

  • Allocate workload set objectives coach and develop QA team.

  • Identify training needs and succession plans aligned with Performance Management.

  • Manage cross-functional projects.

Travel Percentage: None


Required Experience:

Manager

Employment Type

Full-Time

Company Industry

About Company

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