NPI and Validation Engineer (Onsite - Acton, MA)

Insulet Corporation•Acton, MA

21h•Onsite

About The Position

The NPI and Validation Engineer is a critical member of the Global NPI and Validation Engineering team. This team is responsible for transitioning new products into manufacturing (design transfer), providing process validation expertise and support to global manufacturing engineering teams, and providing domestic support for international engineering teams. Regarding design transfer, this role supports the successful introduction of new products, actively engaging with R&D teams to ensure Design for Manufacturing, standardizing design transfer processes, and coordinating Design Transfer activities globally. Regarding process validation support, this role supports the standardization of process validation processes, supporting process development and Design of Experiment activities, and driving cost savings projects. Regarding domestic support for international teams, this role supports the development of global processes for design transfer and manufacturing, planning engineering builds to support R&D activities, and supporting the investigation of quality issues.

Requirements

B.S. and 2+ years of medical device experience OR MS and 1+ year
Experience with structured problem-solving tools (e.g. DMAIC, Six Sigma, Black Belt)
Experience with validation of medical device manufacturing processes and equipment
Experience in data analysis tools such as DOE and process development
Experience and capability working collaboratively under a Quality Management System (QMS), ISO 13485 preferred
The ability to analyze data using various operating systems and programs and to develop intra-department teams to establish goals and take corrective actions to improve performance.

Nice To Haves

A combination of education, training, and experience that results in demonstrated competency to perform the work may be substituted
Hands-on technical ability with assembly methodologies including locational methods, assembly setup, pneumatic actuators, servo motors, limit switches, sensors, robotics, etc.
Mechanical aptitude, technical ability, ability to read and understand technical drawings and manuals.
Technical knowledge of cam driven linkages, discrete component assembly, and automation
Familiarity with machine user interfaces (HMIs / GUIs)
Have strong interpersonal and communication skills
Excellent attention to detail, organizational skills, and rigorous process discipline
Thirst for knowledge and intense curiosity
Decision Making – has a systematic and methodical approach to making decisions, seeks out and explores relevant information, thinks creatively beyond the immediate problem, assimilates facts quickly, challenges assumptions, and considers business implications of potential solutions.
Communication Skills – Conveys information effectively, actively listens, resolves conflict constructively.
Work Organization – Takes a structured, economical approach to resources including time, people, money, and equipment.
Problem Solving – Uses a systematic, methodical approach to gather facts, define problems, generate, and implement solutions.
Initiative – Makes decisions and takes actions appropriately. Willing to take risks as circumstances require.
Planning Skills – Sets goals and priorities, thinks ahead, and identifies activities and resources needed to achieve goals.
Perseverance – Achieves objectives by overcoming difficulties through tenacity and resilience.

Responsibilities

Ensure the timely and effective launch of new products in the manufacturing space thru early collaboration with systems and R&D teams
Assists process improvements in support of Insulet’s primary manufacturing objectives: Best Quality, Best Service, Best Cost
Support Global Manufacturing Engineering in all equipment and process validation activities: FAT, SAT, IQ, TMV, and PQ
Provide domestic support for international teams
Autonomously interpret data to drive cost savings projects
Ensure compliance with safety rules, quality policies, and employee guidelines
Maintain a cGMP compliant environment, operate within FDA guidelines for 21CFR820 manufacturing, and ensure compliance to ISO 13485
Perform other duties as required