8275-Johnson & Johnson Sdn. Bhd. Legal Entity · Workday · 1d
CQ Lead, Malaysia
Petaling Jaya, Selangor, Malaysia- Posted
- 2026-10-07 (1d)
- Place
- Petaling Jaya, Selangor, Malaysia
- Commitment
- Full Time
- Experience
- 5+ YOE
- Source
- Workday (the employer’s own listing)
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Skills in this posting
LESSDocument ControlRoot Cause AnalysisQuality Management SystemPurchasing
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:
Petaling Jaya, Selangor, Malaysia
Job Description:
DePuy Synthes is recruiting for a CQ Lead, Malaysia, located in Petaling Jaya, Malaysia.
This role is responsible for the site management and execution of Quality Systems establishment, implementation and maintenance for Malaysia, including overseeing of Suppliers and Distributors, in order to meet the applicable regulatory and customer requirements and DePuy Synthes (DS) policies and standards.
Essential Job Duties and Responsibilities
Site quality management system activities:
1. Acquisition and divestiture:
• Provides quality support for acquisition and divestiture activities, including change control.
2. Adverse event and/or Health Authority reporting (where applicable)
• Responsible to report adverse events/product quality issues are reported to the health authority in the site if required by local regulation, and ensures robust processes are in place for timely reporting and closure.
3. Audit Readiness, including Inspection management:
• Ensures compliance and audit-readiness of site to DS Quality Policy Standards and applicable local regulatory requirements (i.e. GDP and GDPMD).Lead as site SME for inspection management by coordinating activities related to pre- and post- audit including providing briefing and guidance to all cross functional team, managing audit arrangement and lead in audit response to auditor.
4. Change Control
• Lead for site’s change control management. Responsible to ensure process is followed and records are managed in a timely manner with proper impact assessment, monitoring are taken. Monitors related metrics and initiates actions for improvement
5. Complaints management
• Lead the end to end complaint management for the site. Responsible to prepare and sign customer resolution letters when requested by complainant. Monitors trends, related metrics and initiates actions for improvement.
6. Combination product
• Ensures local regulations and DS standards related to combination products are met.
7. Document control
• Support and ensure site compliance to document lifecycle management.
8. Labeling and Packaging
• Provides Quality support (such as updating quality agreements, issuing redressing instructions) in repack/relabel operation to ensure compliance to internal procedures and local regulations. Monitors related metrics and initiates actions for improvement.
9. NC CAPA Management
• Lead for site’s NC/CAPA management. Responsible to ensure process is followed and records are managed in a timely manner with proper investigation, root cause analysis and corrective and preventive action taken. Monitors related metrics and initiates actions for improvement.
10. New Product Introduction and Product Discontinuation
• To provide Quality support during new product launch and establish any new quality processes to support commercial launch if applicable.
• To work with stakeholders to manage activities related to product discontinuation to ensure compliance to internal and external requirements.
11. Escalation and Field actions
• Oversee the management of Escalations, Field Action, Mock Field Action and Stop shipment applicable to the site.
12. Product Release and Product Returns
• Supports activities related to product inspection and release, temperature excursions and trade returns according to product specifications and internal procedures.
13. Purchasing Control, including POLO
• Support activities related to purchasing controls. Ensures suppliers/POLO are appropriately qualified, monitored and in compliance to up-to-date Quality Agreements, where applicable.
14. QSMR and metrics reporting
• Coordinates key quality metrics reporting. This includes Non-conformance, CAPA, Complaints, Change Control, Audit Actions tracking and monitoring as per timelines.
15. Quality Manual
• Responsible to establish and maintain site’s Quality Manual.
16. Records retention
• Provide guidance to LOCs on record retention process in collaboration with records coordinator.
17. Training Management
• Support and ensure site compliance to GxP training plan for quality system elements covered by the site’s quality manual. This role is also responsible for the metrics, communications, reports and non-conformance related to these areas.
Distributor quality oversight
1. This role is responsible for the execution and compliance of Quality Management Systems elements applicable to the Distributor as required per DS standards and applicable local regulatory regulation, including: product release and returns, handling of storage, temperature controls, traceability, repack relabels, loaner set management, and NC/CAPAs.
2. This role is also responsible for purchasing control activities related to the
distributor such as qualification, audits, and monitoring of distributor quality KPIs.
Required Qualification and Core Competencies for the role:
Requires knowledge and understanding of industry and regulatory standards, and overall DS Quality Systems. Needs experience in tr…
8275-Johnson & Johnson Sdn. Bhd. Legal Entity
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