Senior Technician Engineering (m/f/d)

at  Novanta

Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing.
Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta.
Summary
Professional management of the technical project components and content-
related support of the associated work packages (target definition, definition
of done) in a change project, together with the project manager and the
PE-team.

Primary Responsibilities

• Technical evaluation of product changes
• Development of test and verification plans for product changes and validations based on the technical evaluation.

General Tasks

• Evaluation and documentation of product changes based on the system architecture, considering existing specifications, risk management, regulatory and normative provisions.
• Review of risk management in the context of product changes
• Monitoring the technical progress of product change projects
• Responsible for repeating standard tests of the device as part of product changes.
• Creation and maintenance of technical documentation for own area of responsibility.
• Technical contact for customers and external development partners.
• Control of material and parts list creation/management in the context of product changes.

Required Experience, Education, Skills, Training and Competencies

• Several years of development experience in the field of plastics development or plastics processing
• Independent and interdisciplinary solution finding for projects.
• Knowledge of system development and/or software design
• Development experience in a medically regulated environment; knowledge of the relevant regulations
• In-depth knowledge of plastic materials in medical technology
• Quality-conscious, trustworthy and reliable
• Able to work in a team
• Communicative skills
• Structured and systematic way of working
• SAP knowledge
• Basic knowledge of English (GER-B2)*

Travel Requirements

• Willingness to travel to all locations and business contacts

Physical Requirements

• none

Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.
Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process

Primary Responsibilities

• Technical evaluation of product changes
• Development of test and verification plans for product changes and validations based on the technical evaluation

General Tasks

• Evaluation and documentation of product changes based on the system architecture, considering existing specifications, risk management, regulatory and normative provisions.
• Review of risk management in the context of product changes
• Monitoring the technical progress of product change projects
• Responsible for repeating standard tests of the device as part of product changes.
• Creation and maintenance of technical documentation for own area of responsibility.
• Technical contact for customers and external development partners.
• Control of material and parts list creation/management in the context of product changes