Project Engineer II
Direct Hire
Richmond, VA

About the role:
The Project Engineer II is responsible for managing small to large-scale packaging engineering projects within a cGMP and FDA-regulated manufacturing environment. This role focuses on packaging equipment design, selection, installation, and optimization through identification of opportunities and implementation of effective solutions.

This position requires the ability to independently initiate, plan, and execute projects while also contributing to more complex initiatives. Project Engineer II collaborates cross-functionally to ensure equipment is properly selected, installed, and validated, while meeting production, quality, cost, and compliance objectives.

What you’ll do:
Technical & Project Execution

• Provide engineering support for packaging equipment projects for new and existing products within the  Richmond facility and third-party operations
  

• Design and develop packaging equipment lines and support systems integration
  

• Lead or support installation, commissioning, and verification of packaging equipment
  

• Develop and execute equipment testing and qualification protocols to ensure compliance with company and regulatory requirements
  

• Assist with vendor testing, factory acceptance testing (FAT), and site acceptance testing (SAT)

Project Management

• Initiate, plan, and manage multiple projects simultaneously, including scope, schedule, and budget
  

• Perform cost estimation for equipment, installation, labor, and materials; track and report project costs
  

• Support capital project planning, budgeting, and long-range planning initiatives
  

• Conduct project status updates and present progress to stakeholders and leadership
  

• Review and approve contractor bids, RFIs, and change requests

Cross-Functional Collaboration

• Collaborate with Operations, Quality, Regulatory Affairs, Engineering, Purchasing, and vendors to resolve packaging challenges and implement solutions
  

• Coordinate multi-disciplinary teams (Engineering, EHS, Quality, Production) to ensure successful project execution
  

• Ensure alignment with site standards, best practices, and regulatory requirements

Compliance & Continuous Improvement

• Ensure all activities comply with FDA cGMP and company policies
  

• Support site change control processes for new equipment and process changes
  

• Manage or support the Engineering Verification Process (equipment validation)
  

• Identify opportunities for process improvements, standardization, and new technologies
  

• Promote and exemplify cGMP compliance in all activities

Documentation & Training

• Prepare and maintain project documentation including SOPs, job aids, and technical reports
  

• Maintain accurate project records and history files
  

• Train production staff on new equipment and processes
  

• Serve as a technical resource and mentor to junior team members

Our ideal candidate:
Education & Experience:

• Bachelor’s degree in Mechanical Engineering or related field
  

• 5+ years of experience in a manufacturing environment (pharmaceutical, personal care, or similar preferred)
  

• Experience with equipment design, installation, commissioning, and validation in a cGMP environment

Skills & Abilities:

• Strong project management and organizational skills
  

• Ability to manage multiple projects independently
  

• Strong analytical, troubleshooting, and problem-solving abilities
  

• Effective communication and technical writing skills
  

• Working knowledge of FDA cGMP requirements
  

• Ability to read and interpret P&IDs, process flow diagrams, and technical drawings
  

• Experience with CAD or similar design software preferred
  

• Ability to lead cross-functional teams and influence stakeholders

What we offer:
Competitive salaries with a comprehensive benefits package including Medical, Dental, Vision, Short and Long-Term Disability, Life and AD&D, 401(k), and more.

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