• QA Project Manager Medical Device

    Actalent (Irvine, CA)


    Project Manager - Quality Assurance in M&A

    *The position is 100% onsite in Irvine, CA*

     

    We are seeking a highly experienced Project Manager to lead Quality Assurance (QA) activities for a strategic M&A initiative in the medical device industry. This role demands a strong leader capable of navigating complex situations and collaborating effectively with cross-functional teams, including Regulatory Affairs (RA) and Clinical Affairs (CA). .

    Responsibilities

    + Assemble and lead project teams, assign responsibilities, and identify resources to ensure timely project completion.

    + Capture detailed customer requirements, constraints, and assumptions to define project deliverables.

    + Develop strategy and planning documentation.

    + Estimate, monitor, and manage project budgets throughout the lifecycle.

    + Align stakeholders and team members by setting clear expectations and maintaining a shared understanding of project goals.

    + Identify, assess, monitor, and close project risks proactively.

    + Manage scope, schedule, and cost changes using verification techniques to maintain an accurate and approved project plan.

    + Improve team performance through leadership, mentoring, and motivation to foster cooperation and efficiency.

    + Measure and report project performance using appropriate tools and techniques.

    + Ensure stakeholder alignment and manage resource prioritization.

    + Escalate employee performance and workflow issues as needed.

    + Review and spot-check deliverables to ensure quality and compliance.

    Essential Skills

    + 10+ years of Project/Program Management experience in the medical device industry.

    + Proven ability to analyze and resolve complex process and system issues using independent judgment.

    + Strong interpersonal, communication, and negotiation skills.

    + Ability to build trust and influence mid-level management and present effectively to executives.

    + Skilled in generating and explaining detailed proposals, schedules, budgets, and documentation.

    + Proficient in project management tools and software.

    + Medical device industry experience with a deep understanding of FDA regulations, ISO standards, and global quality systems.

     

    Additional Skills & Qualifications

     

    + PMP or equivalent certification preferred.

    + Experience managing QA activities in M&A environments is preferred.

    + Experience coordinating with Regulatory Affairs and Clinical Affairs teams is preferred.

    Work Environment

    This role is based onsite 5 days a week (8 a.m. - 5 p.m. core hours) in Irvine, CA. The company offers 3 weeks of PTO and a supportive work culture dedicated to quality and compliance in a fast-paced environment.

     

    Job Type & Location

     

    This is a Contract position based out of Irvine, CA.

    Pay and Benefits

    The pay range for this position is $65.00 - $80.00/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 Nov 14, 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 [email protected] (%[email protected]) for other accommodation options.