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Location
In office (Singapore)
Visa
Sponsors visas in United States; no register of this country names it
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 12, 2026. First seen by Alion on Nov 12, 2026. Merit Medical Systems scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Merit Medical Systems is a Nasdaq-listed manufacturer of proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures, headquartered in South Jordan, Utah. Founded in 1987, it serves interventional radiology, cardiology, oncology, endoscopy, dialysis access and critical care, with manufacturing and offices in Tijuana, Galway, Maastricht, Venlo, Richmond and Singapore. Its openings include production operators, quality technicians, clean room supervisors, engineers, account executives and strategic account managers, compliance specialists and support staff.

Work Shift:

DAY

Work Schedule:

800a-530p M-F {8.5}

Why Merit?

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.

ESSENTIAL FUNCTIONS PERFORMED

1. Performs routine engineering work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks.

2. Uses limited amounts of discretionary judgment in making decisions regarding engineering alternatives.

3. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles.

4. Responsible for risk management documentation for assigned product line(s) or processes; and identifying and updating failure modes and related process/product improvements by facilitating teams and implementing required changes.

5. Reviewing, approving and generating Engineering Change Notifications (ECNs) to update or generate: verification, validation, monitoring and inspection methods, procedures, and test protocols; specific to assigned product line(s) and processes and production control(s).

6. Evaluating and participating in the selection of suppliers by monitoring supplier performance, through collection and trending of data and performing supplier quality audits, as required.

7. Reviewing nonconformance records (internal/external) to determine: disposition, root cause and need for corrective and preventive actions.

8. Ensuring containment (identification, segregation and reconciliation) of nonconforming product has been performed, to prevent unintended use.

9. Identifying and implementing any changes necessary to ensure and maintain the continued suitability and effectiveness of the quality management system through the use of: quality policy, quality objectives, audit results, analysis of data, etc.

10. Evaluating the work environment, in which product is manufactured, is adequately environmentally controlled and monitored, with sufficient personnel and safety production controls.

11. May participate in design and development activities.

12. Performs other related duties and tasks as required.

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS

  • Lifting -- Not to exceed 50 lbs. - local practice may apply.
  • Writing
  • Sitting
  • Standing
  • Bending
  • Vision
  • Color perception
  • Depth perception
  • Reading
  • Field of vision/peripheral
  • Fine motor skills
  • Noise
  • Chemical vapors

SUMMARY OF MINIMUM QUALIFICATIONS

  • Education and/or experience equivalent to a Bachelors Degree in Quality Engineering or related field, or a Masters Degree.
  • Strong interpersonal, organizational, and verbal and written communication skills and the ability to work effectively as a team member.
  • Demonstrated working knowledge of 21 CFR 820 (Quality Systems Medical Devices), ISO 13485, ISO14791, and other medical device related standards.
  • Proven ability to work effectively in a team environment through conflict resolution and negotiations.
  • Working knowledge of statistical methodologies, quality control and manufacturing tools, such as applied statistics, lean manufacturing, Six Sigma, etc.
  • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.

PREFERRED QUALIFICATIONS

  • Medical device experience or equivalent experience in a regulated industry.
  • Experience with SmartCAPA, Oracle and Crystal Reports.
  • Experience handling deviations, investigations and CAPAs.

COMPETENCIES

  • Standard engineering techniques/procedures/criteria
  • Special projects/ECN's
  • NC causes/corrective actions/dispositions

COMMENTS

Infectious Control Risk Category II:

The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.

To see more on our culture, go to www.merit.com/careers.

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