Overview
Quality Manager Jobs in Shenzhen, Guangdong, China at Boyd
Title: Quality Manager
Company: Boyd
Location: Shenzhen, Guangdong, China
Job Summary
The Senior Quality Manager is a strategic leader responsible for the overall Quality Management System (QMS) and the quality performance of our products and processes. This role goes beyond traditional QC/QA; it is about embedding quality into the DNA of the company. You will be responsible for developing quality strategy, leading a team of quality professionals, and interfacing with senior leadership to ensure that quality objectives align with and support business goals. The ideal candidate is a proactive leader, an effective change agent, and a subject matter expert in quality principles and regulations.
Key Responsibilitie
sStrategic Leadership & Business Integration
- :Develop, implement, and communicate the long-term quality strategy and roadmap for the organization
- .Establish and monitor Key Performance Indicators (KPIs) and metrics to measure the effectiveness of the QMS and report on quality performance to the executive team
- .Integrate quality principles into all business processes, from design and development to supply chain management and customer service
- .Champion a culture of continuous improvement and quality excellence throughout the organization
.Quality Management System (QMS) Oversight
- :Own, maintain, and continuously improve the company's QMS, ensuring compliance with all applicable standards (e.g., ISO 9001, ISO 13485, IATF 16949, AS9100)
- .Lead all internal and external audits, including regulatory and certification body audits. Serve as the primary management representative
- .Manage the CAPA (Corrective and Preventive Action) program, ensuring robust root cause analysis and effective, timely resolutions
- .Oversee the management review process, prepare and present data on QMS performance to senior management
.Team Leadership & Development
- :Lead, mentor, and develop a high-performing team of Quality Engineers, Analysts, and Inspectors
- .Foster a collaborative environment where the quality team is seen as a valuable partner to engineering, manufacturing, and operations
- .Manage resource allocation, budget, and professional development for the quality department
.Risk Management & Compliance
- :Proactively identify and mitigate quality risks across the product lifecycle and supply chain
- .Ensure compliance with all relevant domestic and international regulatory requirements (e.g., FDA, EU MDR, FAA)
- .Oversee the supplier quality management program, including audits, performance monitoring, and development
.Process Improvement & Customer Focus
- :Utilize Lean, Six Sigma, and other process improvement methodologies to drive efficiency, reduce waste, and improve product quality
- .Act as a central point of contact for critical customer quality issues, ensuring swift and effective resolution and communication
- .Analyze customer feedback and field data to identify trends and drive preventative actions
.
Required Qualifications & Experien
- ceBachelor’s degree in engineering, Life Sciences, Business Administration, or a related field. Master’s degree preferre
- d.10+ years of progressive experience in a quality role, with at least 5+ years in a quality management or leadership positio
- n.Proven track record of successfully implementing, maintaining, and improving a QMS that is certified to a recognized standard (e.g., ISO 9001, ISO 13485
- ).Extensive experience leading and hosting external audits (e.g., FDA, Notified Body, Registrar
- ).Demonstrated experience in leading and developing a technical tea
- m.In-depth knowledge of quality core tools (APQP, PPAP, FMEA, MSA, SPC
- ).Strong financial and business acumen, with experience managing a department budge
- t.Excellent communication, presentation, and interpersonal skills, with the ability to influence at all levels of the organizatio
- n.Certified Quality Manager (e.g., CQM, CMQ/OE) or similar professional certification is highly desirabl
e.Preferred Qualificatio
- nsExperience in Electricals manufacturing industr
- y.Expertise in specific regulatory requirements., 21 CFR Part 820, 21 CFR Part 11, EU MDR, ASPICE
- ).Proven expertise in Lean Six Sigma (Black Belt or Master Black Belt certification strongly preferred
- ).Experience with quality in a new product development (NPD) environmen
- t.Hands-on experience with modern Quality Management Software (QMS) and ERP system
s.