Assistant Engineer, Process

Reposted Yesterday
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Pasir Gudang, Johor Bahru, Johor, MYS
In-Office
Entry level
Healthtech
The Role
Maintains and improves manufacturing processes, equipment, tooling, work instructions, and quality documentation. Supports process validation, risk assessments, SPC, nonconformance investigations, corrective actions, staff training, supplier quality improvements, and cost-reduction initiatives. The role requires collaboration with engineering, quality, research and development, and production teams in optical and electro-mechanical manufacturing environments.
Summary Generated by Built In

Job Summary:

As an Assistant Engineer, you will be responsible for maintaining manufacturing processes and assisting with ensuring production downtime is minimized and quality is maintained. Assist to develops, standardize and optimize process equipment, tooling specifications and manufacturing documentation such as visual aids, assembly and testing instructions and product acceptance criteria to meet product specifications. Involve in designs fixtures, jigs, pokayoke and manufacturing tooling. Able to performs process validations; following IQ/OQ/PQ procedures. Able to lead and comply with Engineers to completes disposition of materials and components; works with suppliers to reduce quality issues. Maintaining and execute cost reduction plans and practices continuous improvement by utilizing best practices; such as lean manufacturing methodologies and/or statistical techniques. 

Duties & Responsibilities:

  • Understand the process requirement of all process and equipment in the production area.
  • Responsible to maintains process work instructions associated with all manufacturing processes such as manufacturing assembly and in-process acceptance procedures.
  • Collaborating with Engineers in developing and implement Visual Aids and Physical Samples on critical steps of the process to indicate proper acceptance criteria.
  • Take charge to trains manufacturing staff to released work instructions.
  • Managed to execute Process Validation Protocols or/and Transference Plans and help Engineers to generates test reports. 
  • Maintains and help Engineers to improve process risk assessments, pFMEA
  • Able to take lead and supports investigation, disposition, and corrective action of non-conforming materials
  • Responsible in identifying areas for improvement, maintaining high levels of manufacturing and product quality

  • Maintaining and sustain the statistical process controls (SPC) for manufacturing operations
  • Responsible for ensuring cost reduction/process improvement programs

Minimum & Preferred Qualifications and Experience:

Minimum Qualifications:

  • · Experience with optical / electro-mechanical assembly and testing

  • · Experience in modern manufacturing principles and techniques

  • · Working knowledge of statistical techniques (e.g., DOE, FMEA, SPC)

  • · Experience in process automation, verification and validation

  • · Excellent communication skills and technical writing abilities

  • · Excellent conceptual, analytical, and problem-solving abilities

  • · Excellent computer skills – CAD software, word processing, and spreadsheets

  • · Ability to be work effectively in cross-functional teams

Preferred Qualifications:

  • Technical experience working in high-volume manufacturing environment.

  • Experience in application of statistical process controls in a manufacturing environment

  • Experience in manual, semi-automated and automation processes, verification and validation

  • Hands-on skills with electro-mechanical troubleshooting and diagnostics

  • Excellent technical writing abilities

  • Good conceptual, analytical, and problem-solving abilities.

  • Good computer skills - CAD, word processing, and spreadsheets.

  • Ability to be part of a team and adept in building and leading teams.

  • Knowledge and experience in FDA QSR requirements and preferably ISO-13485 requirements is an advantages.

  • Experience with planning and executing process validations and managing process risk assessment

  • Knowledge on developing and executing saving projects thought lean manufacturing techniques.

  • Good English communication skills, both verbal and written, and the ability to effectively interface with Research and Development, Quality Assurance, and other functional groups in the organization

Education:

Diploma and B.S. in Mechanical Engineering, Electrical Engineering, Manufacturing, Mechatronics or Industrial Engineering

Physical requirements/Work Environment 

This position primarily works in an office and Production environment. It requires frequent sitting, standing and walking.  Daily use of a computer and other computing and digital devices is required.  May stand for extended periods when facilitating meetings or walking in the facilities.  Some local or international travel is necessary, so requires the ability to operate a motor vehicle, maintain a valid Driver’s license and maintain a valid travel passport. 

The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods.  Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.

Masimo is an Equal Opportunity Employer, We encourage Minorities, Females, Disabled, and Veterans to apply.

 

Skills Required

  • Experience with optical or electro-mechanical assembly and testing
  • Experience with modern manufacturing principles and techniques
  • Working knowledge of DOE, FMEA, and SPC statistical techniques
  • Experience in process automation, verification, and validation
  • Excellent communication and technical writing skills
  • Conceptual, analytical, and problem-solving abilities
  • Computer skills including CAD software, word processing, and spreadsheets
  • Ability to work effectively in cross-functional teams
  • Technical experience in a high-volume manufacturing environment
  • Experience applying statistical process controls in manufacturing
  • Experience with manual, semi-automated, and automated processes, verification, and validation
  • Hands-on electro-mechanical troubleshooting and diagnostic skills
  • Ability to build and lead teams
  • Knowledge of FDA QSR and preferably ISO 13485 requirements
  • Experience planning and executing process validations and managing process risk assessments
  • Experience developing cost-saving projects using lean manufacturing techniques
  • Good English verbal and written communication skills
  • Diploma or bachelor's degree in mechanical, electrical, manufacturing, mechatronics, or industrial engineering
  • Valid driver's license and ability to operate a motor vehicle
  • Valid travel passport and ability to travel locally or internationally

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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