Jobs

Product Quality Engineer

|  Posted On: Jan 23, 2026

location:Marlborough, MA 01752

Duration:6 Months, Contract

mode of work:On-site

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Job Summary

Job Title:  
Product Quality Engineer
Posted Date:  
Jan 23, 2026
Duration:  
6 Months, Contract
Shift(s):  

08:00 - 16:00

Salary ($): 
60.00 - 65.00 per Hourly (compensation based on experience and qualifications)
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Talk to our Recruiter

Name:
 
Meet Yadav

Email:
 
myadav@rangam.com

Phone:
 
650-516-3170

Description

Minimum 1 year working with medical devices or other highly regulated industry, Quality Engineering experience preferred

Job Title:   Product Quality Engineer
       

Organizational Relationships:   Works with Divisional personnel and Costa Rica personnel including Product Quality Engineering (PQE), Post Market Quality Engineering (PMQE), and Post Market Analytics.

 Job Summary

  • Provide Product Quality Engineering support on risk management and product complaint trending.
  • This role will be responsible for reviewing each complaint record individually and identifying the appropriate risk lines and associated severities from the product's Risk Management File (RMF) that relate to what was reported by the complainant and the results of the investigation.
  • In partnership with Product Quality Engineering and Post Market Quality Engineering, the qualified contractor will perform assessments, identify potential updates to the RMF, and perform trend analysis per the applicable quality procedures.

Essential Duties

  • Duties are listed in order of greatest importance. 
  • The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs.  
  • Analyze complaint information and identify hazardous situations and harms reported through complaint information
  • Evaluating content in existing Risk Management Files ensuring all hazardous situations and harms reported through complaint information is adequately captured.
  • Perform trend analysis using Statistical Process Controls per applicable quality procedures.

 Qualifications 

Education   

  • BS in biomedical engineering, mechanical engineering, or health care related discipline

Experience

  • Minimum 1 year working with medical devices or other highly regulated industry, Quality Engineering experience preferred

Skills

  • Experienced with Quality System Regulations, ISO 13485 and 21 CFR 820.
  • Experienced with ISO 14971, Risk Management
  • Basic knowledge of medical terminology and anatomy
  • Basic knowledge of engineering and process terminology