Associate Manager- Life Cycle Management

Why engineering at Stryker?

At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.

Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: https://www.strykercareersblog.com/post/8-reasons-to-join-strykers-engineering-team

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

• Design & develop designs for Legacy products (sustenance Engineering) using engineering principles and medical device Design Control process.
• Experience in leading the team, people management activities.
• Collaborate with NPI and Verification and Validation Team to execute projects .
• Good Understanding of Project management and Product Management .
• Experience in handling Mechanical, Electronics Hardware, Software, and System level Sustenance Engineering activities.
• Value improvement and design optimization activities.
• Knowledge of Engineering System with good understanding of Software Design Cycle and Hardware design Cycle.
• Collaborate with cross functional teams and work with suppliers & contractors.
• Knowledge of Developing designs to meet requirements for performance, reliability, cost, and manufacturability.

• 10- 12 years of work experience, with Bachelors/Masters in engineering.
• Preferred to have candidate with Mechatronics, Robotics, Biomechanics background . Open for Mechanical Candidates with Electronics hardware and software Knowledge .
• Prior experience in leading the team, people management activities.
• PMP Certifications are desirable.
• Understanding of the Medical Device Design control process and sustenance activities .
• Good Understanding of Change Control process, especially ECN/ECR Process.
• Experience in Attending the Change control board and Change Implementation Board Meetings.
• knowledge and understanding of engineering practices and design principles.
• Knowledge of Value Improvement Process and design optimization.
• Actively participate in cross functional teams.
• Ability to apply knowledge of materials and manufacturing processes to product design.
• Excellent written and oral communication skills in English.
• Ability to communicate strategy, plans and technical information to team members.