Senior Engineer II

Werfen•Bedford, MA

29d•$130,000 - $160,000

About The Position

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Position Summary: Using Engineering procedures standard for research and development, carries out assignments associated with research, design, development, support or manufacturing of specific parts, processes, software or components of medical diagnostic systems. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Under the general direction of a functional manager, with moderate latitude for self-direction, operates in one or more areas of responsibility within a specific function.

Requirements

Bachelor's degree in Engineering, Science or a related field
Ten years of product development or relevant experience
Six to eight years of product development or relevant experience for advanced degrees
For internal candidate promotion: Demonstrated proficiency in meeting all competencies of current level and acceptable performance history may be used in lieu of experience
Proficiency in English language required
Some domestic and international travel may be required.
Statistical Analysis (if required by the function)
Root Cause Analysis
Creative Problem Solving
Critical Thinking
Technically adept and confident
Leadership: Accountability, Decision Making, Influence, Communication
Mentoring

Nice To Haves

In vitro medical device experience highly desired.

Responsibilities

Acts as an individual contributor, core team or technical lead for a specific project.
Accountable for the completion of assigned deliverables in accordance with approved schedules.
Authors documentation and participates in activities in support of design control.
Independently plans, performs & prioritizes tasks that are complex in nature, in alignment with corporate goals.
Analyzes and interprets data, identifying trends and formulating the next steps, while effectively performing trade off analysis, if required by the function.
Leads, designs and/or develops one or more of the following: new test methods, specifications, technical apparatus, software and processes for complex components and functions.
Identifies product defects and recognizes outliers in results. Able to explain and document product defects and their impact.
Effectively communicates technical information to a multidisciplinary team in the form of documentation, presentations and technical summaries and promotes collaboration.
Technical expertise in a least 1 area and emerging as a subject matter expert.
Provides technical guidance to and/or supervision of other group members and cross-functional technical teams. Able to mentor others.
Provides technical support for or leads CAPA or complaint investigations.
Independently generates predictable schedules for activities related to the function, understanding cross-functional dependencies.
May review and provide input to deliverables from other functions.
Recommends and leads implementation of improvement initiatives to aid department practices.
May be assigned CAPA ownership.