Địa điểm

Hải Phòng

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

Location
  • Lương

    35 - 45 triệu VNĐ

  • 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

Job Purpose

The Deputy Quality Manager is responsible for supporting the Quality Manager in establishing, maintaining, and improving the Quality Management System (QMS) in compliance with GMP and relevant ISO standards. The role focuses on ensuring cleanroom production quality, regulatory compliance, and continuous improvement during the expansion of medical device manufacturing.

Quality Management & Compliance

  • Assist in managing and maintaining the Quality Management System in compliance with GMP and ISO standards (ISO 13485 / ISO 13484 as applicable).
  • Ensure all production activities meet regulatory and internal quality requirements for medical devices.
  • Participate in preparing, implementing, and updating SOPs, quality manuals, and related documentation.

Cleanroom Management

  • Oversee and manage ISO Class 8 cleanroom operations in accordance with GMP requirements.
  • Ensure cleanroom standards (environmental monitoring, hygiene, contamination control) are strictly followed.
  • Supervise validation, qualification, and routine monitoring of cleanroom facilities and equipment.

Audit & Inspection Support

  • Support internal audits, external audits, and inspections by regulatory authorities and certification bodies.
  • Prepare audit reports, manage corrective and preventive actions (CAPA), and ensure timely closure of non-conformities.

Training & Supervision

  • Provide GMP, ISO, and cleanroom compliance training to production and quality staff.
  • Support the Quality Manager in supervising quality personnel and coordinating cross-functional activities.

Yêu Cầu Công Việc

Education : University degree in Pharmacy (Licensed Pharmacist preferred).

Experience

  • Experience working with GMP-certified manufacturing environments.
  • Practical experience with ISO 13485 (or ISO 13484 as required) standards for medical devices.
  • Proven experience in cleanroom management, preferably ISO Class 8.
  • Strong understanding of GMP requirements related to cleanroom operations and medical device production.

Skills & Competencies

  • Strong knowledge of GMP and cleanroom quality standards.
  • Good documentation, audit, and regulatory compliance skills.
  • Leadership, coordination, and problem-solving abilities.
  • Ability to work under pressure in a regulated manufacturing environment.

Salary & Benefits

  • Salary: Negotiable based on capability and experience
    Range: 35 – 45 million VND/month
  • Professional working environment in a growing medical device manufacturing company
  • Opportunities for career development and advancement
  • 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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