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Transportation & Temp Control - APAC

DePuy Synthes · Chiyoda, Tokyo, Japan

TemporaryOn-sitePosted 7 July 2026
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Job description

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: Quality Job Sub Function: Customer/Commercial Quality Job Category: Professional All Job Posting Locations: Chiyoda, Tokyo, Japan Job Description: DePuy Synthes is recruiting for a Transportation & Temp Control - APAC, located in Singapore, Central Singapore or Chiyoda, Japan or Suzhou, China. Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): Singapore and China - Requisition Number: R-084923 Japan - Requisition Number: R-087022 Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission. The Transportation & Temp Control - APAC supports the effectiveness, compliance, and continuous improvement of the Quality Management System (QMS) across the APAC region. This role partners closely with regional and global QARA stakeholders to ensure quality system processes align with internal requirements, applicable regulations, and global standards. The position plays a critical role in strengthening inspection readiness, enabling consistent quality execution, and supporting the delivery of safe and compliant orthopedic products across APAC markets. Key Responsibilities Support the implementation, maintenance, and continuous improvement of the APAC Quality Management System (QMS) in alignment with global QARA requirements and regional regulations. Coordinate and support QMS activities including document control, change management, CAPA, management review inputs, and quality metrics reporting. Assist with preparation, execution, and follow‑up of internal audits, external audits, and regulatory inspections across APAC markets. Track, trend, and analyze QMS performance data to identify risks, gaps, and opportunities for improvement. Support CQSS initiatives by maintaining quality system documentation, dashboards, and regional tracking tools. Partner with regional QARA, Operations, and Commercial teams to ensure consistent understanding and application of QMS requirements. Support the rollout of global QMS updates and ensure timely regional implementation and communication. Contribute to inspection readiness activities and continuous improvement projects across APAC. Qualifications Education Bachelor’s degree required in Engineering, Life Sciences, Quality, Regulatory, or a related discipline. Advanced degree preferred. Experience and Skills Required: Typically 0–2 years of professional experience in Quality, Quality Systems, Regulatory Affairs, or a regulated industry environment. Foundational knowledge of Quality Management Systems and continuous improvement concepts. Experience supporting documentation, data analysis, or compliance‑related activities. Ability to work effectively in a cross‑functional, regional environment. Proficiency with Microsoft Office tools (Excel, PowerPoint, Word). Preferred: Experience in the medical device, pharmaceutical, or other highly regulated industry. Exposure to ISO 13485, FDA QSR, or comparable regulatory frameworks. Experience supporting audits, inspections, or CAPA processes. Familiarity with electronic QMS tools or quality data systems. Experience working in a regional or global operating model. Strong analytical, organizational, and problem‑solving skills. Other: Language: Proficiency in English required; additional APAC languages preferred. Travel: Limited. Certifications: Quality‑related certifications (e.g., ISO, Six Sigma, CQE) preferred but not required. 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 plans. In 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. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. #LI-Hybrid #DePuySynthesCareers Required Skills: Preferred Skills: Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment

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