• Project Engineer AVI

    Actalent (Greenville, NC)


    Description

    We are seeking a highly motivated and experienced Project Engineer to lead and support initiatives involving automated visual inspection systems within our pharmaceutical manufacturing operations. This role is critical to ensuring product quality, regulatory compliance, and operational efficiency through the implementation and optimization of cutting-edge inspection technologies.

    Key Responsibilities

    • Lead the design, installation, commissioning, and validation of automated visual inspection equipment for pharmaceutical products (e.g., vials, syringes, ampoules).

    • Collaborate with cross-functional teams including Quality Assurance, Validation, Maintenance, and Production to ensure seamless integration of inspection systems.

    • Develop and manage project timelines, budgets, and resource allocation for equipment upgrades and new installations.

    • Author and review technical documentation including URS, FRS, IQ/OQ/PQ protocols, and change controls.

    • Troubleshoot and optimize inspection systems to improve detection accuracy, reduce false rejects, and enhance throughput.

    • Ensure compliance with cGMP, FDA, EU Annex 1, and other applicable regulatory standards.

    • Interface with equipment vendors and service providers to evaluate new technologies and coordinate service activities.

    • Train operations and maintenance personnel on equipment functionality and best practices.

     

    Skills

     

    project engineering, automated visual inspection, pharmaceutical

    Additional Skills & Qualifications

    • Bachelor’s degree in Engineering (Mechanical, Electrical, Industrial, or related field).

    • 3+ years of experience in pharmaceutical manufacturing, with a focus on automated visual inspection systems.

    • Hands-on experience with inspection platforms such as Seidenader, Eisai, Antares, or similar.

    • Strong understanding of pharmaceutical packaging formats and defect classification.

    • Familiarity with validation lifecycle and regulatory documentation requirements.

    • Excellent problem-solving, communication, and project management skills.

    • Proficiency in data analysis tools and manufacturing software (e.g., SCADA, MES, PLC/HMI interfaces).

    Preferred

    • Experience with serialization and track-and-trace systems.

    • Knowledge of lean manufacturing and continuous improvement methodologies.

    • Ability to manage multiple projects in a fast-paced, regulated environment.

     

    Job Type & Location

     

    This is a Contract position based out of Greenville, NC.

    Pay and Benefits

    The pay range for this position is $45.00 - $65.00/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 Greenville,NC.

     

    Application Deadline

     

    This position is anticipated to close on Nov 20, 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.