Job Title: Program ManagerJob Description This role involves leading projects that implement manufacturing strategies for new Neurovascular products, specifically focusing on venous thromboembolism clot removal. The Program Manager will be accountable for all design transfer activities, ensuring that products are delivered on time, within scope, with quality, and on budget. The role demands effective management of project and product costs, alongside proactive identification and mitigation of project risks. Responsibilities + Activate and motivate the project team to drive project success and achieve goals on time. + Collaborate closely with R&D, production, and suppliers to understand end-customer needs and ensure successful project implementation. + Innovate and improve the current project management tools and PMO governance. + Ensure stakeholder alignment and resource prioritization. + Handle employee performance issues and escalate any workflow issues. + Review deliverables and conduct spot checks to maintain quality standards. + Manage EU MDR Plus or base business or sustaining type of roles, including tasks such as changing labels, GTIN, and transitioning software systems. Essential Skills + Proven expertise in project management. + Experience in the medical device industry. + Stakeholder alignment and resource prioritization skills. + Knowledge of EU MDR regulations. + Labeling and regulatory affairs proficiency. + PMP certification or equivalent preferred. Additional Skills & Qualifications + Bachelor's Degree in Engineering. + 6+ years of post-graduate work experience. + 6-8+ years of project management experience. + Experience in new product introduction. Work Environment This position is based onsite in Irvine, CA. The role offers 2 weeks of paid time off and includes 10 client-paid holidays. The work environment is dynamic and collaborative, encouraging innovation and improvement in project management practices. Pay and Benefits The pay range for this position is $60.00 - $70.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Irvine,CA. Application Deadline This position is anticipated to close on Jul 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.