Program Manager

Program ManagerJoin a leading team in the medical device manufacturing industry as a Program Manager. This role is pivotal in managing customer programs from initial concept to full commercialization in a regulated environment. As the main liaison between customers and internal teams, you will ensure projects are delivered on time, within budget, and adhere to stringent quality and regulatory standards.ResponsibilitiesLead customer programs through product development, validation, commercialization, launch, and production transfer.Develop and manage project plans, schedules, budgets, resource plans, and risk mitigation strategies.Coordinate cross-functional teams across Engineering, Manufacturing, Quality, Operations, Supply Chain, Regulatory, R&D, Tooling, and Customer Service.Serve as the primary customer contact, providing project updates, managing expectations, and resolving program risks and issues.Support new product introductions, validation activities, manufacturing readiness, tooling transfers, and commercialization efforts.Drive accountability, issue resolution, and project execution across multiple concurrent programs.Track project financials, timelines, KPIs, and documentation while maintaining program visibility for leadership and customers.Ensure compliance with FDA regulations, ISO standards, and internal quality systems.Essential SkillsExperience in medical device manufacturing, ideally class II or class III.Engineering Degree, preferably in biomedical engineering.Strong communication skills, able to handle difficult conversations and provide solutions.Proficiency in team development and mentoring newer engineers.Project management experience, with knowledge of product lifecycle management.Familiarity with FDA regulations and ISO standards.Experience in medical device manufacturing, contract manufacturing, plastics processing, extrusion, injection molding, assembly, automation, or similar production environments.PMP certification or equivalent project management experience.Additional Skills & QualificationsBachelor's degree in Engineering, Business, Operations, Life Sciences, or a related field.3+ years of program or project management experience in a regulated manufacturing environment.Experience with project management tools and ERP systems is preferred.Lean Manufacturing or Six Sigma certifications are a plus.Work EnvironmentThis position is based fully onsite at a manufacturing facility. Join a fast-growing medical device manufacturer with plans to double its workforce over the next year. Employees have the opportunity to work with innovative products, advance their careers, and make a meaningful impact in a rapidly expanding organization.Job Type & LocationThis is a Permanent position based out of Charlotte, NC.Pay and BenefitsThe pay range for this position is $90000.00 - $150000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Benefits & Perks Medical, Dental & Vision Insurance 401(k) with Company Match Paid Time Off (PTO) & Paid Holidays Life & Disability Insurance Health Savings Account (HSA) & Flexible Spending Accounts (FSA) Employee Assistance Program (EAP) Career Growth & Advancement Opportunities Training and Professional Development Fast-Growing Medical Device Manufacturing Environment Exposure to Innovative, Life-Impacting ProductsWorkplace TypeThis is a fully onsite position in Charlotte,NC.Application DeadlineThis position is anticipated to close on Oct 1, 2026.