R and D Engineer - Stryker (lakeland, FL)
Job Title R and D Engineer Division Stryker Sustainability Solutions Business Unit U.
S.
Business Sub:
Functions New Product R and D Country United States State FL City Lakeland Shift 1st Job Description The R and D Engineer designs, develops, and improves new processes for medical devices and directs the testing and evaluation of medical devices.
DUTIES and
Responsibilities:
? Advanced understanding of project leadership skills needed to effectively lead a multiple tasked and cross functional team projects to completion.
? Advanced understanding of project management principles to effectively complete assignments and achieve desired outcomes.
? Increased project ownership and accountability ? Uses team management skills to lead the design group during product development through product launch ? Directs development of an action plan and estimates requirements for resources :
management, tasks, budgets, labor, materials, and time required to complete projects.
? Monitors progress of development project and compares actual costs with estimates.
? Leads design team to modify plans as appropriate if problems arise.
? Prepares communication in weekly reports, status updates, detailing progress and costs for management.
? Discusses project status reports at monthly project reviews with executive team and design review meetings.
? Advanced ability to generate detailed project plans, multitask, and fast tracking of project tasks.
? Plans and directs new product development ? Ability to effectively interact within a team environment and with other departments such as Quality, Operations, Regulatory Affairs, Mfg.
Engineering, Customer Service, Marketing, Sales, as well as external customers and suppliers.
? Establishes test protocols specified by customer input, national and international standards, and regulatory requirements.
? Directs and facilitates the testing of new products to verify product reliability.
? Interaction with production/manufacturing for design transfer to production floor ? Leads the development of technical protocols and reports.
? Improve/support existing processes.
? Advanced knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions.
EDUCATION and
Experience:
? Bachelors degree in an engineering or science field.
? 1:
3 years of practical experience in the medical device industry or 5
years exp.
in medical device industry plus advanced degree.
(medical device company preferred) ? Advanced understanding of Statistical Methods and Project Management Principles (formal training preferred) ? In:
depth knowledge of medical terminology/concepts related to medical devices.
? Knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions.
? Proficient in managing projects and project management principles to effectively complete assignments and achieve desired outcomes.
? Proficient in project management, ownership and team member supervisory skills.
? Excellent organizational skills and ability to plan/prioritize activities.
? Ability to work independently or with a team.
? Strong verbal and written communication skills; ability to present issues, plans and objectives.
? Ability to work in fast paced organization, meeting multiple deadlines and succeeding under pressure is a must.
? Motivated, resourceful, ambitious, enthusiastic and attentive to detail.
? Proficient in Microsoft Word, Excel, Power Point, Outlook, Project, Visio ? Exposure Source:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
S.
Business Sub:
Functions New Product R and D Country United States State FL City Lakeland Shift 1st Job Description The R and D Engineer designs, develops, and improves new processes for medical devices and directs the testing and evaluation of medical devices.
DUTIES and
Responsibilities:
? Advanced understanding of project leadership skills needed to effectively lead a multiple tasked and cross functional team projects to completion.
? Advanced understanding of project management principles to effectively complete assignments and achieve desired outcomes.
? Increased project ownership and accountability ? Uses team management skills to lead the design group during product development through product launch ? Directs development of an action plan and estimates requirements for resources :
management, tasks, budgets, labor, materials, and time required to complete projects.
? Monitors progress of development project and compares actual costs with estimates.
? Leads design team to modify plans as appropriate if problems arise.
? Prepares communication in weekly reports, status updates, detailing progress and costs for management.
? Discusses project status reports at monthly project reviews with executive team and design review meetings.
? Advanced ability to generate detailed project plans, multitask, and fast tracking of project tasks.
? Plans and directs new product development ? Ability to effectively interact within a team environment and with other departments such as Quality, Operations, Regulatory Affairs, Mfg.
Engineering, Customer Service, Marketing, Sales, as well as external customers and suppliers.
? Establishes test protocols specified by customer input, national and international standards, and regulatory requirements.
? Directs and facilitates the testing of new products to verify product reliability.
? Interaction with production/manufacturing for design transfer to production floor ? Leads the development of technical protocols and reports.
? Improve/support existing processes.
? Advanced knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions.
EDUCATION and
Experience:
? Bachelors degree in an engineering or science field.
? 1:
3 years of practical experience in the medical device industry or 5
years exp.
in medical device industry plus advanced degree.
(medical device company preferred) ? Advanced understanding of Statistical Methods and Project Management Principles (formal training preferred) ? In:
depth knowledge of medical terminology/concepts related to medical devices.
? Knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions.
? Proficient in managing projects and project management principles to effectively complete assignments and achieve desired outcomes.
? Proficient in project management, ownership and team member supervisory skills.
? Excellent organizational skills and ability to plan/prioritize activities.
? Ability to work independently or with a team.
? Strong verbal and written communication skills; ability to present issues, plans and objectives.
? Ability to work in fast paced organization, meeting multiple deadlines and succeeding under pressure is a must.
? Motivated, resourceful, ambitious, enthusiastic and attentive to detail.
? Proficient in Microsoft Word, Excel, Power Point, Outlook, Project, Visio ? Exposure Source:
.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
