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Product Analysis Engineer

In Massachusetts / United States

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Product Analysis Engineer   

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JOB TITLE:
Product Analysis Engineer
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Burlington Massachusetts / United States

JOB DESCRIPTION :

Role: Product Analysis Engineer

Location: Burlington, MA

Duration: 10 Months on W2

Top Skills:

  • Excellent Written/Oral communication
  • Time Management
  • Ability to get work done with minimal supervision Preferred Education
  • Electrical Engineering Degree
  • Biomedical Engineering with a heavy course load in electrical engineering.

Responsibilities:

  • Communicates verbally and in writing both internally and externally to Abbott regarding the information needed specific to new product complaints (e.g. physicians, hospital personnel, sales representatives, international offices), initiates and manages the complaint file Investigates complaints/events in a timely manner
  • Maintains accurate entry of complaints in database Records condition of returned products including observations, photographs Coordinates product testing/analysis with other departments and external consultants
  • Prepares technical reports of analysis/findings Tracks returned products within the database, as appropriate. Works collaboratively with cross-functional groups (e.g. QEs, R&D) on evaluation trends or findings Interprets technical product specifications,
  • Device History Records or measurements obtained Utilizes safe bio-hazard and chemical handling practices at all times Participates in the cross-functional complaint review groups on a regular basis or as requested (e.g. cross[1]functional complaint teams, rapid customer response team, Risk Management meetings) Lead the investigation, resolution, and prevention of product and process non conformances
  • Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member) Lead in the completion and maintenance of risk analysis

Qualifications:

  • BS degree in Electrical Engineering; 0-2 years' experience Engineering experience preferred Knowledge of global regulations for medical device reporting and medical terminology is a plus Strong written and oral communication skills are required.
  • Strong organizational and follow-up skills, as well as attention to detail.

Preferred Qualifications: Advanced degree Prior medical device experience Knowledge of FDA, GMP, ISO 13485, and ISO 14971 ASQ CQE or other related certification will be a plus.

Position Details

Apr 18, 2021
S16174660637612817
Massachusetts / United States
Burlington
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Product Analysis Engineer    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Role: Product Analysis Engineer

Location: Burlington, MA

Duration: 10 Months on W2

Top Skills:

  • Excellent Written/Oral communication
  • Time Management
  • Ability to get work done with minimal supervision Preferred Education
  • Electrical Engineering Degree
  • Biomedical Engineering with a heavy course load in electrical engineering.

Responsibilities:

  • Communicates verbally and in writing both internally and externally to Abbott regarding the information needed specific to new product complaints (e.g. physicians, hospital personnel, sales representatives, international offices), initiates and manages the complaint file Investigates complaints/events in a timely manner
  • Maintains accurate entry of complaints in database Records condition of returned products including observations, photographs Coordinates product testing/analysis with other departments and external consultants
  • Prepares technical reports of analysis/findings Tracks returned products within the database, as appropriate. Works collaboratively with cross-functional groups (e.g. QEs, R&D) on evaluation trends or findings Interprets technical product specifications,
  • Device History Records or measurements obtained Utilizes safe bio-hazard and chemical handling practices at all times Participates in the cross-functional complaint review groups on a regular basis or as requested (e.g. cross[1]functional complaint teams, rapid customer response team, Risk Management meetings) Lead the investigation, resolution, and prevention of product and process non conformances
  • Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member) Lead in the completion and maintenance of risk analysis

Qualifications:

  • BS degree in Electrical Engineering; 0-2 years' experience Engineering experience preferred Knowledge of global regulations for medical device reporting and medical terminology is a plus Strong written and oral communication skills are required.
  • Strong organizational and follow-up skills, as well as attention to detail.

Preferred Qualifications: Advanced degree Prior medical device experience Knowledge of FDA, GMP, ISO 13485, and ISO 14971 ASQ CQE or other related certification will be a plus.