Staff Engineer

Work Flexibility: Hybrid What you will do: • Independently research, design,
develop, modify, and verify components, modules and sub-systems for medical
devices Translate user needs to design inputs/ specifications and produce
complex system level designs with some guidance. • Conduct or design advanced
prototyping and testing. Analyze and correct complex product design issues using
independent judgment • Working on multiple projects simultaneously in product
engineering such as gap assessments, design changes, manufacturing transfers,
product development, regulatory or business-driven projects, etc. • Execution of
NC CAPA implement design controls & risk controls.Experience in executing NPD
projects involving the complete product development life cycle phases from
concept to launch. • Advance solutions by applying in-depth knowledge of
customer needs, market and competitive offerings and apply detailed knowledge of
clinical procedures to author design inputs • Support Voice of Customer sessions
internally and with clinicians. Demonstrate developing financial acumen • Be
proficient with and mentor others in usage of industry standards, including
design requirements and test strategies per applicable regulations • Lead
creation and refinement of engineering documentation, such as the Design History
file. Follow and mentor others on R&D procedures like design controls and risk
management, per the • Work cooperatively with R&D, Quality, Manufacturing,
Regulatory, Clinical, Marketing and Project Management to ensure project success
• Identify and support the creation of or improvements to procedures, policies,
processes, systems, and technology. Support and execute segments of complex
multifunctional teams to advance projects through the design /development/launch
process • Deliver high quality results with passion, energy and drive to meet
business priorities. Collaborate with cross-functional teams to build
partnership to achieve business objectives What you will need- Required Skills :
• Bachelor of Science in Engineering, Mechanical Engineering & 6-9 years of work
experience • Strong technical ability to develop and optimize designs for
mechanical / electro-mechanical assemblies incorporating DFM principles;
creating engineering drawings, models, applying GD&T and CAE tool. • Experience
with analysis tools, specifically tolerance analysis, CFD and FEA using ANSYS
software preferred. Competency in statistics, process capability, design of
experiments, including statistical applications such as Minitab, etc. Preferred
Qualifications: • Adept at applying knowledge of materials and manufacturing
processes to product design and ability to communicate moderate complexity plans
and technical information to team members • Good working knowledge of CAD
applications (Creo/SolidWorks/UniGraphics) • Experience in working with
regulated industries like Medical devices, Aerospace, Automotive etc.
Understanding of medical device standards and regulations is preferred. Good
understanding of designing of jigs & fixtures and inspection methods. Travel
Percentage: 10% Stryker is one of the world’s leading medical technology
companies and, together with its customers, is driven to make healthcare better.
We offer innovative products and services in Orthopaedics, Medical and Surgical,
and Neurotechnology and Spine that help improve patient and hospital outcomes.
We are proud to be named one of the World’s Best Workplaces! For more
information, visit: www.stryker.com Work Flexibility Remote – Role allows you to
work the majority to 100% of time from an alternate workplace. These roles could
have travel expectations, and you must work within the country of the job
requisition location. Field-based – You can expect to regularly work a majority
to 100% of time at customer facilities and has a set territory or expectation to
travel within a set boundary. Almost all sales roles would likely be qualified
as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc
flexibility may be available depending on role, level, and job requirements.
Manufacturing roles and any role that requires physical presence at the office
would qualify under this category. Hybrid – You can expect to regularly work in
both an alternate workplace and a Stryker facility. Roles that are partially
remote or co-located would qualify as hybrid, and the expectation to be onsite
would be defined and agreed upon by your manager/supervisor.