Please join us as:
Project Manager, NRO Development
SUMMARYThe Project Manager will coordinate New Technology and New Product Development efforts, consistent with medical device new product develpment customer requirements. The Project Manager will interface with Senior Management, Line Management, and external customers and supplier to assure success against Key Performance Indicators.
PRIMARY JOB RESPONSIBILITIES- Manages international development teams to assure technology and development efforts are achieved in alignment with established project and portfolio commitments.
- Develops and manages project plans, schedules, and budgets for NPD and technology projects.
- Develops and maintains strong relationship with internal and external suppliers. Lead the effort to identify, evaluate, and select relevant suppliers to meet project goals.
- Interacts with internal and external customers to assure scope of projects meet Voice-of-Customer needs.
- Provides regular updates to Senior Management, Product Management, Operations, and other departments to assure project deliverables are on track with intended goals. Using relevant KPIs, provides risk-based analysis of project to assure that project goals are met within constraints of given budgets and timelines.
- Works with Design and Quality assurance, leading the effort to assure medical devices are developed in compliance with relevant Quality Management Systems. May assist with product and QM audits, as necessary.
- Other duties may be assigned at the discretion of the manager.
REQUIRED QUALIFICATIONS - BS Degree in engineering in the field of Electrical, Biomedical, Mechanical, or related engineering discipline.
- Minimum 4 years' experience in project management of medical devices or similarly regulated industry.
- Experience in project management of international and global development teams.
- Demonstrated track record of technical project management leadership.
- Strong communication skills, with a focus on team collaboration/development.
- Strong group facilitation and mediation skills.
- Industry-related knowledge of medical device development.
PREFERRED QUALIFICATIONS- PMP or similar certification.
- Familiarity with Agile and other project management methodologies.
- Direct knowledge of FDA and MDR regulations.
- Experience with ISO 13485 and/or 21CFR820 compliant Quality Management Systems.
LEADERSHIP RESPONSIBILITIESWork with MST customers as project liaison between the development team and stakeholders.
Coordinate with team leads to drive project and establish estimates of project time and materials.
No direct personnel management required.
TRAVEL REQUIREMENTSMust be able to travel internationally and domestically, less than 15% of the time.
WORK ENVIRONMENT If onsite, this role is based in a temperature controlled professional office setting, which may include an office or cubicle with quiet to moderate noise level. If remote, the work environment is the employee's residence. Work may need to be completed on campus in a lab, or manufacturing environment such as clean room or warehouse. Personal protective equipment is required in the clean room and may be needed in a lab. The noise level in the lab, and manufacturing environments are quiet to moderate. The role may travel to vendors, customers, external training, expos, industry or product events, and networking events shifting the work environment.
This position is Hybrid, based in out Lake Oswego, Oregon office.
