Địa điểm

Hải Phòng

A, ĐT362, Câu Hạ, xã Quang Trung, An Lão, Hải Phòng

Location
  • Lương

    Thỏa thuận

  • Kinh nghiệm

    Không yêu cầu kinh nghiệm

  • Số lượng

    1

  • Hết hạn nộp

    14/02/2026

Phúc lợi

  • Chế độ bảo hiểm
  • Du Lịch
  • Chế độ thưởng
  • Chăm sóc sức khỏe
  • Đào tạo
  • Tăng lương

Mô tả Công việc

Position Summary

The QC Supervisor is responsible for overseeing day-to-day quality control operations to ensure that all medical devices meet internal specifications, customer requirements, and regulatory standards (ISO 13485, GMP). This role supervises QC staff, ensures timely inspection and testing of materials and finished products, manages documentation, and supports continuous improvement of quality systems.

1. QC Operations & Supervision

  • Lead, train, and supervise QC inspectors/technicians.
  • Plan and allocate daily inspection/testing activities for incoming materials, in-process production, and finished goods.
  • Ensure adherence to approved inspection procedures, work instructions, and sampling plans.
  • Monitor QC lab/inspection area and ensure proper calibration and maintenance of equipment.

2. Compliance & Documentation

  • Ensure QC activities comply with ISO 13485, GMP, and internal SOPs.
  • Review and approve QC records, inspection reports, test results, and COAs.
  • Maintain accurate documentation for audits, CAPA investigations, non-conformities, and change controls.
  • Handling internal and external audits (ISO13485, GMP, notified bodies, customer audits).

3. Quality Issue Management

  • Lead investigations of non-conforming materials and products.
  • Initiate NCRs, participate in root cause analysis, and contribute to corrective/preventive actions.
  • Communicate quality issues to production, engineering for timely resolution.

4. Continuous Improvement

  • Identify gaps in QC processes and recommend improvements for efficiency and compliance.
  • Support implementation of statistical techniques for process monitoring
  • Contribute to validation activities (process, equipment, test method validation).

5. Cross-Functional Collaboration

  • Coordinate with Production, Engineering, Supply Chain, and R&D to ensure quality standards are met.
  • Provide inputs for supplier quality issues and qualification when needed.
  • Support new product development

Yêu Cầu Công Việc

  • Bachelor’s degree in Science, Engineering, Pharmacy, or related field.
  • 3–5+ years of experience in Quality Control within the medical device or pharmaceutical industry.
  • Supervisory or team-lead experience preferred.
  • Strong knowledge of ISO 13485, GMP, and risk management
  • Experience with measurement tools, inspection techniques, and QC testing equipment.
  • Familiarity with CAPA, NCR, calibration, and 3Q-validation processes.
  • Strong analytical, communication, and leadership skills.
  • Proficiency in MS Office; experience with QMS software is an advantage.
  • Candidates currently living or able to live long-term in Hai Phong - proximity to the company is an advantage

Thông tin khác

  • Bằng cấp: Đại học
Địa điểm Thôn Câu Hạ A, Xã Quang Trung, Huyện An Lão, Thành phố Hải Phòng, Việt Nam
Thông tin công ty
  • Qui mô công ty:
  • Loại hình hoạt động: Trách nhiệm hữu hạn
  • Website:
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Giới thiệu về công ty

Our company is built on a foundation of entrepreneurship stemming from our owner and CEO of over 30 years, Mr. Jeff Whitely. Jeff was a young, innovative individual who identified the importance of a natural and drug-free method of healing when he took the helm of Rapid Aid over three decades ago. Starting out with limited resources and space, but armed with a vision and drive to succeed, Jeff has since turned Rapid Aid into the world’s leading designer and manufacturer in the hot and cold therapy industry.

From our humble beginnings over four decades ago, Rapid Aid has grown exponentially to work across multiple continents and with the largest global distributors and retailers.

We now occupy three state-of-the-art, wholly-owned manufacturing facilities in Mississauga, Ontario, Canada, Danyang, Jiangsu, China and most recently, Hai Phong City, Vietnam. With distribution capabilities spanning three continents our multi-production systems are working in tandem every day to produce millions of units a month, healing bumps and bruises around the globe.

Continuing in the forward-thinking tradition at Rapid Aid, Mr. Curtis Scott, our long-time team member and General Manager of Rapid Aid China, recently became a partner in the company. Curtis leads our Asia production facilities, working closely with our trusted local management and maintaining an intrinsic link to our Canadian operations. Curtis and our team in East China and Vietnam have consistently improved plant automation, personnel training and corporate social responsibility, all to the satisfaction of our strict international standards.

Over our many years of focusing on a single healthcare category, we hold dozens of international patents, patents pending and trademarks across three continents. Our global team is deeply specialized, and committed to developing our sole concentration at Rapid Aid hot and cold therapy products. Moving forward, Rapid Aid continues to drive expertise and innovation in our industry, and we look forward to Making It Better for our clients and the public for decades to come.

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