Assistant Project Manager

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Job Description:

DePuy Synthes is recruiting for a(n) Assistant Project Manager located in Shanghai Shanghai China.

This role leads and delivers cross-functional Quality Regulatory and Compliance projectssupporting China Operations and Distribution within QARA International. This role ensuresprojects are planned executed and delivered on time within scope and budget and incompliance with internal quality systems and external regulatory requirements. Thisposition plays a critical role in enabling compliant market access distribution continuityand operational excellence for DePuy Synthes in China.

Key Responsibilities
Plan organize and control QARA projects supporting China commercialoperations distributor and health authority requests ensuring adherence to scopetimelines budgets and quality compliance.
Develop and maintain detailed project plans schedules risk registers andcommunication plans; proactively manage dependencies and risks.
Lead the cases related to post market collaboration project requested by healthauthorities which includes but not limited to: Investigation assistance from theDrug Administration or the Market Supervision Bureau Sampling and etc.
Promote China GSP related policy shaping via connection with internal expertsindustry experts and associations etc. Accelerate post market excellencemanagement in China
Coordinated process optimization within QARA organization and supportcommercial projects with cross-functional department as quality expert.

Qualifications
Education
Bachelors degree required (e.g. Engineering Life Sciences Quality RegulatoryAffairs or Business).
Advanced degree (e.g. Masters or MBA) preferred.

Experience and Skills
Required
Typically 68 years of relevant work experience in Quality project or programmanagement within regulated environments (medical devices pharmaceuticals or
healthcare preferred).
Demonstrated experience managing cross-functional projects from planningthrough execution and closure.
Strong coordination and communication skills
Proven ability to manage schedules risks and stakeholder expectationssimultaneously.
Can be adapted to the changing environment and work under challenges.

Preferred
Experience supporting China operations and/or distributor-based business models.
Experience coordinating external partners or vendors within project frameworks.
Familiarity with GSP or ISO-based quality systems and regulatory expectations formedical devices.
Certified Lead auditor is preferred.
Strong communication and influencing skills across functions and seniority levels.

Other
Languages: Fluent in Mandarin and English (written and spoken).
Travel: Limited domestic travel within China; limited international travel as needed.
Certifications: Project Management certification preferred (not required).

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Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months subject to legal requirements including consultation with works councils and other employee representative bodies as may be required regulatory approvals and other customary conditions and approvals. Should you accept this position it is anticipated that following conclusion of the transaction you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes programs policies and benefit that case details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

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