Company Name:-
Abiomed

Job Location:-
Danvers, MA 01923

Job Summary:-
Abiomed, an innovative medical device company, is focused on recovering hearts and saving lives.

We have a single guiding mission: “Patients First.

” With corporate headquarters in Danvers, Massachusetts, offices in Aachen & Berlin, Germany and Tokyo, Japan, Abiomed’s 1,700 employees form one of the fastest growing medical technology companies in the world.

Abiomed attracts and retains exceptional talent with our collaborative culture, passion for our work, and a strong commitment to employee professional development.

This position is responsible for various quality design engineering functions in support of development such as design assurance engineering activities, as well as manufacturing process development, risk management, design validation and verification, statistical analysis with an emphasis on Medical Devices single use devices, reusables and software.

Primary Duties and Responsibilities:
The following duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all-inclusive.

The omission of a specific duty or responsibility will not preclude it from the position:
Support and Lead Design Assurance engineering activities in support of Abiomed’s Product Development and Life Cycle processes including design controls, quality planning, risk assessments/analysis/management, design reviews, test method development and validation, design and process verification and validation test plans and reports, post-market monitoring, investigations, follow-up and reporting
Ensure that Design controls are compliant with all relevant regulations (FDA, 13485, PMDA).

Ensure that FDA and other regulatory knowledge and experience is applied to risk and testing assessments
Work with manufacturing engineering to ensure necessary process controls are in place for design changes.

Review and approve Engineering Change Orders (ECO) and support the material review board (MRB) processes as needed
Act as an effective team member in the execution of Quality functions in compliance with FDA QSRs (Design Control, CAPA, etc), ISO 13485, MDD, CMDR, CMDCAS and other national and international quality and regulatory requirements and standard
Contribute to the design,

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