Job Information
Steris Senior Project Manager Job Details | Steris Corporation in United States
Senior Project Manager
Req ID: 44396
Job Category: Service/Technical Services
Mentor, OH, US, 44060
Description:
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position Summary
STERIS is looking for a Senior Project Manager to be responsible for the overall direction, coordination, implementation, execution, control and completion of multiple medical device new product/service development projects that include the following: new products, line extensions and product improvements (which also includes business continuity and product support projects) ensuring consistency with company strategy, commitments and goals. This person will also be responsible for managing complex new product development projects with multi-functional teams; responsibilities include the planning of all project activities according to defined product development and stage gate processes, coordination of project team activities to meet project deliverables, FDA/ISO requirements, and the management of the overall project schedule, resource requirements, risk assessment, business case, and budget, including progress reporting and reviews with senior management.
Duties
Leads and drives the planning and implementation of multiple projects, varying in size and scope and recommends revisions in project work plans as appropriate to meet changing needs and requirements.
Facilitates the definition of projects’ scope, goals and deliverables.
Assembles Cross Functional Teams (CFT) and leads them through the development process for projects of varying complexity, including new medical devices and services.
Identifies and defines resource requirements needed and recommends assignments for individual CFT member responsibilities.
Manages day-to-day operational aspects of projects and scopes.
Leads Voice of Customer initiatives and works closely with Product Management to define customer/market requirements for new products development
Works with various department heads to assure alignment of CFT member objectives and work schedules to assure projects deliverables are achieved.
Effectively applies Stage/Gate methodology and enforce project standards to drive project completion.
Duties - cont'd
Leads and manages creation of Gate deliverables and Gate presentations with project team and senior management.
Ensures project documents and Gate deliverables are complete, up-to-date, and stored appropriately.
Complies with and helps to enforce standard New Product Development policies and procedures.
Work with CFTs to develop project schedules and tracks project deliverables to completion
Leads and coordinates market release inventory requirements with Supply Chain and Materials/Logistics departments.
Work with Quality, Regulatory, and Document Control to ensure all project documentation requirements are fulfilled for product release.
Develops and manages budgets for the project including resource loading, external expenses and capital requirements.
Work with Product Managers, Sales Team, Product Specialists, Manufacturing and Engineers in creating design and manufacturability process validation plans and lab tests. Attends CFT market research sessions when appropriate.
Required Experience
Bachelor’s degree with ten+ year’s successful demonstrated experience managing complex new product development projects is required.
Technical degree in the sciences or engineering fields highly beneficial
Project Management Professional (PMP) or New Product Development Professional (NPDP) certification(s) a plus.
Demonstrated planning and organizational skills with background and experience in Design Control and Stage Gate methods is required.
Experience with FDA guidance, ISO 13485 regulations and CE Mark requirements is highly preferred. Experience with Medical Device development is highly desired.
Must be a proficient user of Microsoft Project (or similar), Excel, Power Point, Visio, and Word.
Possess ability to conduct market research via internet.
Up to 15% domestic travel is required.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries.
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.
Req ID: 44396
Job Category: Service/Technical Services
Mentor, OH, US, 44060
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