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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:

Hello,

Hope you are doing great.
This is Mubeena from Intellectt INC; we have an immediate opportunity. Please find the below job description and if you are interested, please forward your resume to mubeena@intellectt.com

Role: Product Analysis Engineer

Location: Burlington, MA

Duration: 10 Months

Note: Manager is looking only for LOCAL CANDIDATES of MA

We are seeking a high-caliber Quality Engineer I to conduct complaint investigation management and all activities pertaining to product complaints about Mechanical Circulatory Support Devices. This includes, but is not limited to receiving and investigating reports of worldwide complaints/events; entering information into the complaint database; supporting filing and response to medical devices reports with various regulatory agencies; participating on cross-functional teams, and providing information on the product complaints, including data extracted from the complaint database to various teams (e.g. Regulatory, Quality Engineering). This QE 1 role will also have the opportunity to expand development in the area of quality engineering methodologies and providing quality engineering support within new product development, manufacturing, manufacturing transfers, and/or system/services support.

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 nonconformances

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

Other Duties:

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.

Performs other related duties and responsibilities, on occasion, as assigned.

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.

Candidate must be able to work well independently and on teams in a busy department while managing multiple ongoing tasks and investigations simultaneously.

Advanced computer skills, including statistical/data analysis and report writing skills Experience working in a broader enterprise/cross-division business unit model preferred.

Ability to work in a highly matrixed and geographically diverse business environment.

Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with the ability to effectively communicate at multiple levels in the organization. Multitasks prioritizes and meets deadlines in a timely manner.

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

Top 3 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.

Position Details

POSTED:

Aug 09, 2021

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16174660652852829

LOCATION:

Massachusetts / United States

CITY:

Burlington

Job Origin:

CEIPAL_ORGANIC_FEED

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!

Hello,

Hope you are doing great.
This is Mubeena from Intellectt INC; we have an immediate opportunity. Please find the below job description and if you are interested, please forward your resume to mubeena@intellectt.com

Role: Product Analysis Engineer

Location: Burlington, MA

Duration: 10 Months

Note: Manager is looking only for LOCAL CANDIDATES of MA

We are seeking a high-caliber Quality Engineer I to conduct complaint investigation management and all activities pertaining to product complaints about Mechanical Circulatory Support Devices. This includes, but is not limited to receiving and investigating reports of worldwide complaints/events; entering information into the complaint database; supporting filing and response to medical devices reports with various regulatory agencies; participating on cross-functional teams, and providing information on the product complaints, including data extracted from the complaint database to various teams (e.g. Regulatory, Quality Engineering). This QE 1 role will also have the opportunity to expand development in the area of quality engineering methodologies and providing quality engineering support within new product development, manufacturing, manufacturing transfers, and/or system/services support.

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 nonconformances

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

Other Duties:

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.

Performs other related duties and responsibilities, on occasion, as assigned.

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.

Candidate must be able to work well independently and on teams in a busy department while managing multiple ongoing tasks and investigations simultaneously.

Advanced computer skills, including statistical/data analysis and report writing skills Experience working in a broader enterprise/cross-division business unit model preferred.

Ability to work in a highly matrixed and geographically diverse business environment.

Ability to work within a team and as an individual contributor in a fast-paced, changing environment. Ability to leverage and/or engage others to accomplish projects. Strong verbal and written communications with the ability to effectively communicate at multiple levels in the organization. Multitasks prioritizes and meets deadlines in a timely manner.

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

Top 3 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.


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