Project Engineer II

FAREVA RICHMOND INCRichmond, VA
13dOnsite

About The Position

The Project Engineer II is responsible for independently managing small to large-scale engineering projects in one or more packaging areas within our cGMP and FDA-regulated facility. This role requires strong technical expertise, project leadership, and the ability to deliver solutions that improve production efficiency, ensure compliance, and support long-term business objectives. As a Project Engineer II, you will serve as a subject matter expert (SME) for packaging equipment design, installation, and validation, while also mentoring less-experienced engineers. You will balance hands-on technical work with project coordination, budgeting, and cross-functional leadership.

Requirements

  • Bachelor’s degree in Mechanical Engineering, Packaging Engineering, or related field.
  • 5–7 years of experience in a manufacturing or packaging engineering role, preferably within cGMP-regulated environments.
  • Demonstrated expertise in equipment commissioning, validation, and change control processes.
  • Proven ability to lead cross-functional project teams and independently manage complex projects.
  • Strong project management and organizational skills.
  • Ability to interpret P&IDs, process flow diagrams, and engineering drawings.
  • Proficiency in CAD or similar design programs.
  • Excellent communication skills, both written and verbal.
  • Strong problem-solving and analytical skills with attention to detail.
  • Commitment to safety and regulatory compliance.

Nice To Haves

  • Experience in aerosol or pharmaceutical packaging technology is strongly preferred.

Responsibilities

  • Lead engineering projects for packaging equipment installations, upgrades, and system integrations for new and existing products.
  • Provide advanced packaging line design services, including process flow analysis, equipment layout, and systems integration.
  • Drive standardization and continuous improvement initiatives, incorporating the latest FDA and cGMP guidelines.
  • Develop, review, and execute equipment testing and qualification protocols to ensure compliance.
  • Manage vendor selection, testing, and oversight of equipment installation and verification.
  • Lead multi-disciplinary project teams (Engineering, EHS, Quality, User Groups) to ensure successful project execution.
  • Prepare and manage project budgets, forecasts, timelines, and resource allocations; track expenditures against targets.
  • Support development of capital budgets, long-range master plans, and requests for capital projects.
  • Provide training to production staff on new equipment and updated procedures.
  • Manage and maintain site Engineering Verification processes and validation documentation.
  • Review and approve contractor bids, RFIs, and change requests.
  • Mentor junior engineers and serve as a resource for Packaging Services and Operations.
  • Exemplify and promote cGMP compliance in all activities.

Benefits

  • Fareva provides competitive salaries and a comprehensive benefits package, including Medical, Dental, Vision, Short- and Long-Term Disability, Life and AD&D, 401(k), and additional offerings.
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