EngineeringContractOn-site

Development Quality Engineer II

Westford, Massachusetts1 openingPosted December 9, 2022
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Our Medical Device client in Westford, Massachusetts is currently looking for an Engineer- Degreed IV/Senior Engineer to work on a 12-24 months contract with the possibility of extension/Direct hire. The selected person will be working 8 am- 5 pm Monday to Friday.

 

Verbal and written communication, interpersonal, teamwork, individual contributor, multi-task, strong organizational, advanced computer skills

 

Education: Bachelor-level degree in an Engineering Discipline or other technical field experience

 

Duties: participate in or lead teams in supporting quality disciplines, decisions, and practices, lead on-time completions of design control deliverables, support on-time execution of Quality Plans for internal product development process (PDP), OEM-based Clinical Product Development (CPDP) and design change projects, accountable for generation of PDP design verification test plans/reports for product/system requirements, lead or support Risk Management activities from product concept through commercialization, including generation of risk management plans/reports, completion and maintenance of hazard analysis, FMECA's and Cybersecurity risk assessments, lead identification of essential outputs and generate Essential Output reports, accountable for completion of labeling verification activities and labeling verification reports, work with design engineering in the completion of customer/system/product requirements, work with design engineering in the completion of product verification and validation, endure DHF content completion, integrity and regulatory & standards compliance, collaborative communication resolving gaps, complete document change request reviews in a timely and objective manner, identify and implement effective process control systems to support the development, qualification and on-going manufacturing of products to meet or exceed internal and external requirements, assist in the implementation of assurances, process controls and CAPA systems designed to meet or exceed internal and external requirements, assist in tech development and execution of streamlined business systems which effectively identify and resolve quality issues, apply sound, systematic problem solving methodologies in identifying, prioritizing, communicating and resolving quality issues, support all company initiatives as identified by management and in support of quality management systems (QMS), Environmental Management Systems (EMS) and other regulatory requirements, additional duties may be identified by functional management based on the current project/business objectives.

 

WHAT WE OFFER

 

  • At Abbott, you can have a good job that can grow into a great career.

 

  • A fast-paced work environment where your safety is our priority (Include for Manufacturing roles only)

 

  • Health care Insurance

 

  • 401(k) retirement savings with a generous company match

 

  • The stability of a company with a record of strong financial performance and a history of being actively involved in local communities

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