Senior Project Manager

Acumed-ffe1f67; Hillsboro (OR); On-site; USD 130,000 - 170,000; Full time

Job summary

Acumed LLC in Hillsboro, Oregon seeks a Senior Project Manager to independently plan, manage, and execute multiple complex NPI projects, leading cross-functional Product Development Teams from initiation to implementation.

You will set objectives, scopes, schedules, budgets, and resources, drive risk management, validations, design reviews, and ensure DHF compliance with FDA/ISO requirements, while guiding stakeholders and mentoring junior PMs.

Qualifications

• Bachelor’s degree in Engineering or related field required.
• 8–10 years NPI project management in regulated environment.
• PMP or equivalent certification preferred.

Responsibilities

• Lead 3–7 large, complex NPI projects from initiation through implementation.
• Establish objectives, scope, schedules, budgets, resources, and deliverables.
• Manage risk, design reviews, RCA, and corrective actions.
• Maintain DHF in line with FDA/ISO requirements.
• Communicate status and risks to executives and stakeholders.
• Mentor other Project Managers and support PM processes.

Skills

Leadership

Cross-functional coordination

Project risk management

Stakeholder management

Mentoring

Communication

Problem-solving

FDA/ISO knowledge

MS Project

Education

Bachelor’s degree in Engineering or related field

MS/MBA preferred

PMP certification preferred

Tools

MS Project

SAP

ERP systems

PLM software

Job description

Acumed LLCAs a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best.Location: Hillsboro, OregonJob ScopeThe Senior Project Manager (SPM) independently plans, manages, and executes multiple complex New Product Introduction (NPI) projects simultaneously. This role leads cross-functional Product Development Teams (PDTs) from project initiation through implementation, ensuring objectives for scope, schedule, cost, quality, and risk are achieved. The SPM partners with Program Management, Product Management, functional leaders, and other stakeholders to align projects with portfolio goals and product requirements.Duties/ResponsibilitiesLead 3–7 large, complex NPI projects simultaneously from initiation through implementation.Establish project objectives, scope, schedules, budgets, resources, and deliverables; manage scope changes throughout the project lifecycle.Lead cross-functional Product Development Teams and coordinate with functional leaders to ensure appropriate resources and expertise.Drive project risk management, validation and verification activities, design reviews, technical problem solving, and corrective actions.Ensure project documentation and Design History Files (DHF) are complete and maintained in accordance with FDA and quality requirements.Facilitate customer preference, design review, and product validation labs.Monitor project performance and develop recovery plans when projects fall behind scope, schedule, budget, or quality objectives.Communicate project status, risks, and priorities to executives, sponsors, and key stakeholders.Partner with Program Management and Product Management on product roadmaps and process improvements.Mentor and provide guidance to other Project Managers.Support project management, change management, ERP/SAP, and PLM processes and training.QualificationsBachelor’s degree in Engineering or related field with 8–10 years of experience; MS/MBA and PMP preferred. Equivalent experience with PMP certification may be considered.Demonstrated NPI project management experience in an engineering/manufacturing environment producing regulated durable goods such as medical devices, high technology, or defense.Experience leading complex cross-functional projects and working with internal/external stakeholders and customers.Experience in a formal gated product development/project management environment.Knowledge of FDA and ISO regulations.Demonstrated leadership, communication, problem-solving, stakeholder management, and mentoring skills.High proficiency with MS Project or equivalent project management software required.Experience with project management and product development tools, including design reviews, root cause analysis, work breakdown structures, and corrective action methods.SAP or other ERP experience preferred.Familiarity with medical device or similar regulated product development environments.General understanding of financial analysis, market research, pricing, and product launches.Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to [e-mail], and please be sure to include the title and the location of the position for which you are applying.