Staff Engineer – Mechanical

Stryker

Who we want:

  • Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to Retrofit, Simplify, Standardize, and Automate.
  • Self-directed imitators. People who take ownership of their work/ Project and need no prompting to drive productivity, change, and outcomes.
  • Goal/ Project-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
  • Delivers results.  A driven player who collaborates and sets high goals for personal achievement along with organizational success.  He/she measures success against the best internal and external benchmarks

What you will do:

  • Product development, value improvement and customized product development.
  • Medical device design and development, orthopedic background.
  • Project management along with proven record of working with global teams.
  • Application of GD&T along with very strong CAD skills (preferably Creo).
  • Design calculations and Finite Element Analysis (FEA).
  • Medical device verification and validation.
  • Design management / Change Controls, NC/CAPA process.
  • Lead the team, support, and develop team members.
  • ECN / ECR Process, DHF maintenance, manufacturing & Change Control Procedures.
  • Communicating frequently across all project stakeholders.
  • Management of data using Windchill or PLM tool.
  • Material selection with respect to international standards.
  • Design and Risk Management documentation.

What you will need:

  • 7 – 11 years of work experience with educational background in Bachelors/Masters  in Mechanical Engineering
  • Strong understanding of project management along with proven record of working with global teams.
  • Strong background of product development, value improvement and customized product development experience
  • Strong knowledge of medical device design and development, preferably with orthopedic background.
  • Understanding the verification and validation of medical devices.
  • Expertise in CAD modelling and detailing using Creo.
  • Expertise in Windchill or PLM tool.
  • Design calculations and Finite Element Analysis (FEA).
  • Very good Knowledge of GD&T.
  • Knowledge of ECN / ECR Process, DHF maintenance, manufacturing process & Change Control Procedures
  • Good understanding of different standards, related to medical devices as per FDA or similar.
  • Knowledge of material selection and hands on experience on feasibility study.
  • Good understanding of ISO14971 & ISO13485.
  • Actively participate in cross functional teams
  • Demonstrated ability to apply knowledge of materials and manufacturing processes to product design.
  • Proven track record around working within a global team and employing excellent interpersonal, communication and presentation skills.
  • Ability to support and develop team members.

To apply for this job please visit careers.stryker.com.