Medical Device Complaint Investigation & Failure Analysis Engineer (Class IIIII Devices) (JP15369)
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Job Location:
Thousand Oaks, CA - USA
Hourly Salary:
$ 42 - 47
Posted on:
10 hours ago
Vacancies:
1 Vacancy
Job Summary
Job Title: Medical Device Complaint Investigation & Failure Analysis Engineer (Class II/III Devices) - (JP15369)
Location: Thousand Oaks CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Complaints Trending Group
Duration: 1 year (with likely extensions and/or conversion to permanent)
Posting Date: 05/11/26
Pay Rate: $42 - $47/hour W2
Notes: Only qualified candidates need apply. Hybrid must be on site 2 3 days per week. Standard hours.
3 Key Consulting is hiring a Medical Device Complaint Investigation & Failure Analysis Engineer (Class II/III Devices) for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
The ideal candidate for this role will have at least 5 years of experience performing complaints handling and failure analysis investigations within a medical device environment specifically class II or class III devices. They should be proficient with ISO systems risk analysis processes and protocol or report writing.
A bachelors degree in engineering or sciences such as chemistry physics or biology is strongly preferred though candidates with other educational backgrounds who possess robust laboratory experience will also be considered. Experience working in biohazard lab settings is a plus but not mandatory. Excellent written and verbal communication skills along with strong presentation abilities are essential as the role involves regular presentations to internal teams. Candidates must have a background in medical devices biotech or biopharma industries and must be local able to commute onsite 23 days per week (ideally residing within Los Angeles Orange or Ventura Counties). This role will begin as a one-year contract with the potential for extension.
Engineer - Complaints Technical Investigator:
Requires a combination of working remote and going onsite 2 to 3 times per week (average) for complaint returns assessment and/or laboratory equipment setup development and validation of test methods.
Job Description
Our client is currently seeking an Engineer - Complaints Technical Investigator in our Complaints Trending and Investigation group.
The Engineer - Complaints Technical Investigator conducts forensic evaluations of complaint units for Standard and Advanced complaint investigations associated with product design and/ or usability issues. This role understands customer/ patient use of clients packaged and/or distributed products as well as manufacturing processes for these products. Responsibilities also include helping with Root Cause Analysis investigation lab infrastructure equipment setup and method development and validation.
Why is the Position Open
Supplement additional workload on team
Top Must Have Skills:
Day to Day Responsibilities:
Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
Red Flags:
Interview process:
A total of three interviews are planned all to be conducted via phone. Interviews can begin as soon as possible based on candidate availability.
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Location: Thousand Oaks CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Complaints Trending Group
Duration: 1 year (with likely extensions and/or conversion to permanent)
Posting Date: 05/11/26
Pay Rate: $42 - $47/hour W2
Notes: Only qualified candidates need apply. Hybrid must be on site 2 3 days per week. Standard hours.
3 Key Consulting is hiring a Medical Device Complaint Investigation & Failure Analysis Engineer (Class II/III Devices) for a consulting engagement with our direct client a leading global biopharmaceutical company.
Job Description:
The ideal candidate for this role will have at least 5 years of experience performing complaints handling and failure analysis investigations within a medical device environment specifically class II or class III devices. They should be proficient with ISO systems risk analysis processes and protocol or report writing.
A bachelors degree in engineering or sciences such as chemistry physics or biology is strongly preferred though candidates with other educational backgrounds who possess robust laboratory experience will also be considered. Experience working in biohazard lab settings is a plus but not mandatory. Excellent written and verbal communication skills along with strong presentation abilities are essential as the role involves regular presentations to internal teams. Candidates must have a background in medical devices biotech or biopharma industries and must be local able to commute onsite 23 days per week (ideally residing within Los Angeles Orange or Ventura Counties). This role will begin as a one-year contract with the potential for extension.
Engineer - Complaints Technical Investigator:
Requires a combination of working remote and going onsite 2 to 3 times per week (average) for complaint returns assessment and/or laboratory equipment setup development and validation of test methods.
Job Description
Our client is currently seeking an Engineer - Complaints Technical Investigator in our Complaints Trending and Investigation group.
The Engineer - Complaints Technical Investigator conducts forensic evaluations of complaint units for Standard and Advanced complaint investigations associated with product design and/ or usability issues. This role understands customer/ patient use of clients packaged and/or distributed products as well as manufacturing processes for these products. Responsibilities also include helping with Root Cause Analysis investigation lab infrastructure equipment setup and method development and validation.
Why is the Position Open
Supplement additional workload on team
Top Must Have Skills:
- Experience with protocol and report writing process and test development and execution and design of experiments
- Experience in leading continuous improvement activities by driving the implementation of process and product quality improvement initiatives
- Strong technical writing and interpersonal skills
Day to Day Responsibilities:
- Lead evaluation of returned product product reserve sample inspections batch records and review of complaint histories and trends.
- Provide input to engineering for product improvements.
- Partner with device engineering to develop structured failure analysis processes and tools for current and future device platforms.
- Lead root cause analysis to identify the failure mode for clients products and associated components due to product complaint.
- Perform failure analysis to identify root cause using processes and tools such as fishbone diagrams 5 Whys risk assessments such as FMEAs Fault Tree Analysis or tolerance analysis. Additional equipment such as CT scanners Instron tensile test machines and SEM may be used.
- Lead cross functional ideation of design solutions to reduce complaints based on output of root cause analysis determine feasibility of options through testing and analysis develop business plans for implementation.
- Generate final reports in accordance with established procedures which may include data collection and statistical analysis of the data.
- Help with investigations lab equipment setup develop and provide equipment training to personnel develop and validate test methods and develop SOPs for equipment use.
Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
- Masters Degree in Science
- 5 years of experience in complaints or failure analysis investigation within a development or manufacturing environment working with Medical Devices ideally Class II and Class III
- Understand customer / patient use of clients packaged and/or distributed products
- Understand manufacturing processes for clients packaged and/or distributed products
- Proven experience with medical devices
- Demonstrated Six Sigma proficiency specifically for root cause analysis methodology
- Experience with risk management per ISO 14971 (System Risk Analysis User Risk Analysis DFMEA/FMEA and other Risk Management tools)
- Experience with protocol and report writing process and test development and execution and design of experiments
- Experience in leading continuous improvement activities by driving the implementation of process and product quality improvement initiatives
- Strong technical writing and interpersonal skills
Red Flags:
- Candidates may be screened out if their resumes include vague or inconsistent descriptions of responsibilities or do not demonstrate hands-on investigation root cause analysis or laboratory experience.
- Poorly organized resumes or those that do not reflect strong communication skills or alignment with role requirements (including onsite availability) may also deter interview consideration.
Interview process:
A total of three interviews are planned all to be conducted via phone. Interviews can begin as soon as possible based on candidate availability.
We invite qualified candidates to sendyour resume to. Ifyou decide that youre not interested in pursuing this particular position please feel free to take a look at the other positions on our You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.
Regards
3KC Talent Acquisition Team
Required Experience:
IC
