Paterson, New jersey
Project Manager, Medical Product -- PMO Job Opening in Paterson, New jersey - Our client, a global medical technology company that specializes in improving patient care and patient safety, is looking for a Project/Product Manager to work within their PMO managing projects around launching a new business platform that will continue the company's growth. This is an outstanding opportunity to join a company with a start-up mentality, growth, and creativity that has solid financial resources of a Fortune 500 type company. This is NOT a Software Development role. Software Development PMs will not be considered.
This is a mid-level PMO Manager who will drive a team of functional professionals with multiple functions. It will include resources from external partners. The PM will have overall accountability for project planning and execution, leading up to successful launch and commercial success of products.
Responsibilities:
Lead product development efforts using many processes and tools. Accountable for delivery, technical excellence and process effectiveness of product development activities.
Make sure that products are developed within the company's development processes and design control procedures.
Responsible for project plan, work breakdown structure, contingency plans. Skilled in the use of various project management software/tools.
Leads multiple small to medium scale projects.
Act as primary contact on Development Agreements and Projects. Interacts with senior external personnel on technical matters often requiring coordination between resources.
Manage project communications.
Manage project resources and make sure they can participate at the level needed for project success.
Communicate project team plans and results at project review meetings. Make sure that senior management are aware of any project issues, etc as they develop.
Develop and manage project budgets, schedules and work plans. Participate in portfolio road mapping exercises, concept phases, etc.
Qualifications:
BA/BS REQUIRED. Degree in science, engineering or similar discipline a plus. Project Management certification a plus but not required.
8 years experience working in a product development environment, including design control and process validation. Pharmaceutical, Medical Device, Medical technology experience highly preferred.
Experience leading cross functional teams.
Ability to build relationships with business partners, external stakeholders etc.
Solid understanding of product development process and innovation within an ISO13485 or CFR820 part 21 environment.
Experience with plastic design and injection molding is a plus.
This is NOT a Software Development PM role. Responses with a Software Development PM background will not be acknowledged and will be immediately rejected.
Candidates must be able to work in the US WITHOUT SPONSORSHIP, now and in the future.
Job Type: Full-time
Salary: $100,000.00 to $112,000.00 /year
Required education:
Bachelor's
Required experience:
experience in ISO13485 or CRF820 part 21 environments: 2 years
project management in pharma, medical devices, medical technology: 8 years
Product Management: 5 years
Required licenses or certifications:
PMP or similar Project Management certification
ability to work in US without sponsorship now and moving forward
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