Role: Engineer I Product Analysis (Electronics Lab)
Location: Burlington MA
Experience: 01 years (Entry level)
PayRate: $2530/hr on W2
100% Onsite Must be Local Candidate (Need to be available for Onsite interview) This is an entrylevel Post Market role which will handle complaint
investigations Will be a combination of office and lab work with 1/3 desk work
and 2/3 lab work Will require PPE/Gowning: Head and beard covers shoe covers
gloves mask etc. Will be working with deadlines and crossfunctional teams A
Bachelors degree in Engineering (Electrical or Biomedical is preferred)
Engineering work experience is preferred for up to one year preferably can
have 2 years of experience but no more than that Masters Degree is fine but No
PhDs please Ideal Candidate is one who has done Coop or Internship Will extend
and/or convert based on performance and budget Top Skills: 1) Time Management
2) Strong Communication verbal and Technical Writing 3) ability to multitask
work independently and with other teams
Main Purpose of Role Perform failure analysis on explanted biomedical implant product. Provide technical expertise to the Product Analysis
Laboratory. Analyzes failures develops and implements investigative protocols to identify root causes performs circuit
analysis performs device and component level failure analysis.
Main Responsibilities Perform failure analysis on explanted longterm biomedical implant product.
Work requires the application of theoretical principals evaluation ingenuity and creative/analytical techniques to identify
route cause failure mechanisms.
Must be able to meet deadlines on multiple assignments and be able to operate in a diverse crossfunctional team environment.
Proactive in finding quality improvements related to Failure Analysis
May serve as lead and assign work to less experienced personnel and serves as a mentor when assisting less experienced lab
staff in solving more complex problems.
Works cross functionally and collaboratively with Product Development Engineering Manufacturing and Product Surveillance.
Aides in definition of test equipment as required to accomplish quality responsibilities.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS)
Environmental Management Systems (EMS) and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations other regulatory requirements Company policies operating procedures processes and task assignments.
Maintains positive and cooperative communications and collaboration with all levels of employees customers contractors
and vendors.
Qualifications: - Bachelors Degree in Engineering is Required
- Electrical or Biomedical Engineering is preferred
- Engineering work experience is preferred
Knowledge of global regulations for medical device reporting and medical terminology is a positive
Strong written and oral communication skills are required
Candidate must be able to work well independently and on teams in a busy department while managing multiple ongoing tasks and investigations simultaneously
Multitasks prioritizes and meets deadlines in a timely manner
Strong organizational and followup skills as well as attention to detail.