Manager, Manufacturing Engineering

Posted 2 Days Ago
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Pasir Gudang, Johor Bahru, Johor, MYS
In-Office
Senior level
Healthtech
The Role
Manage development, validation, and transfer of manufacturing processes, equipment, tooling, and procedures for medical devices. Lead process design and launches, oversee process validations (IQ/OQ/PQ), implement Lean/Six Sigma, drive PFMEA and SPC, support production problem-solving, and coordinate cross-functional teams to improve manufacturability and product quality.
Summary Generated by Built In

Job Summary:

The Manufacturing Engineering Manager is responsible for managing the development, improvement, and validation, of new and existing manufacturing processes, equipment, tooling, and fixtures.  This position leads and/or supports production transfers from Masimo HQ and Operations to Malaysia manufacturing plants, implements and supports/utilizes affective manufacturing methodologies, such as Lean/Six Sigma following international regulatory standards (e.g. 21 CFR, Part 820 and ISO 13485:2003). Manages all engineering projects and resolves engineering problems. You will leverage your technical experience and skills to guide the team in the evaluation of product reliability performance and driving improvement on challenging technical problems. 

Duties & Responsibilities:

  • Responsible for driving and executing on process design, development and launch of new products

  • Manage the design/specification/purchase/installation of the Company’s assembly equipment and tooling;

  • Coordinate the day to day support to production (Customer claims, problem solving, deviations, NCR, yields, process & equipment issues…) to ensure the process is enabled to achieve the operation goals;

  • Coordinate the formulation and release of all pertinent Manufacturing Assembly Procedures, Acceptance Procedures, Inspection Procedures for all personnel in the Operation;  May rewrite processes to improve detail, incorporate visual aids, with the intent of improving the overall quality of Masimo products;

  • Coordinate performance of process validations (IQ, OQ, PQ) including generating protocols and reports in accordance with 21 CFR Part 820 FDA guidelines;

  • Review and approve protocol and written reports.

  • Provides guidance and/or approval of workgroup technical approaches, products and processes

  • Establish Statistical Process Controls for Manufacturing Operations;

  • Coordinate development of Process Failure Mode and Effects Analyses (PFMEA);

  • Coordinate development and implement lean manufacturing processes to build new products and improve existing processes;

  • Oversee initial product builds (engineering units, pilot units, process validation units) and coordinate a smooth transfer of new products into production;

  • Develop manufacturing plans, project timelines, requirements, specifications and process flow;

  • Work closely with design engineering to proactively influence designs for better manufacturability;

  • Must be able to travel domestically and internationally;

  • Perform special projects as requested

 

Minimum & Preferred Qualifications and Experience:

Minimum Qualifications:

  • Five or more years of related experience, with technical staff management experience and project management experience involving coordination of cross-functional teams;

  • Experience in leading process and equipment development projects to completion.;

  • Excellent conceptual, analytical, and problem-solving ability;

  • Experience with electromechanical assembly and testing

  • Experience with Design for Manufacturability and Assembly (DFMA);

  • Basic device software knowledge Experience with statistical techniques (e.g., DOE, SPC)

  • Excellent computer skills - CAD, word processing, and spreadsheets;

  • Good communication skills, both verbal and written, and the ability to effectively interface within a cross-functional team environment;

  • Experienced in modern manufacturing principles and techniques;

  • Will be required to travel both domestically and internationally, on a periodic basis;

  • Must be PC literate, have excellent organizational and communication skills;

 

Preferred Qualifications:

  • Knowledge and experience in 21 CFR, Part 820 and ISO 13485:2003 requirements.

  • Experience with semiconductor component packaging

  • Knowledge and experience in CGMP requirements and preferably MDA and ISO medical device requirements;

  • Experience with electrical/optical products

 

Education:

Bachelor’s degree in engineering: Mechanical, Electrical, Manufacturing or Industrial Engineering is required. 

 

Skills Required

  • Bachelor's degree in Mechanical, Electrical, Manufacturing, or Industrial Engineering
  • Five or more years related experience with technical staff management and project management
  • Experience leading process and equipment development projects to completion
  • Experience with electromechanical assembly and testing
  • Experience with Design for Manufacturability and Assembly (DFMA)
  • Basic device software knowledge
  • Experience with statistical techniques (e.g., DOE, SPC) and establishing SPC
  • Experience with process validations (IQ, OQ, PQ) and writing/approving protocols and reports
  • Excellent computer skills (CAD, word processing, spreadsheets)
  • Excellent communication, organizational, and cross-functional interfacing skills
  • Experience in modern manufacturing principles, lean manufacturing, and PFMEA development
  • Willingness and ability to travel domestically and internationally periodically
  • Knowledge and experience in 21 CFR Part 820 and ISO 13485:2003
  • Knowledge and experience in cGMP and MDA and ISO medical device requirements
  • Experience with semiconductor component packaging
  • Experience with electrical/optical products

Masimo Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Masimo and has not been reviewed or approved by Masimo.

  • Healthcare Strength Comprehensive medical, dental, and vision coverage is offered alongside company‑paid life insurance at 2x salary and long‑term disability coverage. The package reflects broad core health protection.
  • Leave & Time Off Breadth Policies include 15 days of paid vacation to start, up to 10 paid holidays, 40 hours of sick time, and defined paid parental leave components. This structure provides clear, multi‑category time‑off coverage.
  • Wellbeing & Lifestyle Benefits An EAP, corporate discounts, and onsite amenities such as a café, wellness center, and gym are available at certain locations. These perks enhance day‑to‑day support where onsite access exists.

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The Company
HQ: Irvine, California
3,639 Employees
Year Founded: 1989

What We Do

Masimo (NASDAQ: MASI) is a global medical technology company that develops and produces a wide array of industry-leading monitoring technologies, including innovative measurements, sensors, patient monitors, and automation and connectivity solutions. Our mission is to improve life, improve patient outcomes, reduce the cost of care, and take noninvasive monitoring to new sites and applications. Masimo SET® Measure-through Motion and Low Perfusion™ pulse oximetry, introduced in 1995, has been shown to outperform other pulse oximetry technologies in over 100 independent and objective studies, which can be found at www.masimo.com/evidence/featured-studies/feature. Masimo SET® is estimated to be used on more than 200 million patients around the world each year and is the primary pulse oximetry at all 10 top U.S. hospitals as ranked in the 2025 Newsweek World’s Best Hospitals listing. Additional information about Masimo and its products may be found at www.masimo.com.

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