Senior Project Engineer - GMP Biotech Facilities

Catalent Pharma Solutions

Harmans (MD)

On-site

USD 90,000 - 110,000

Full time

5 days ago
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Benefits offered by this job

Medical, dental, and vision benefits
Tuition reimbursement
Competitive PTO and holidays

Job summary

Catalent Pharma Solutions in Harmans, MD is seeking a Senior Project Engineer to lead capital projects in a GMP environment. You will coordinate scheduling, documentation, and cross‑department communication to ensure compliance and successful execution, reporting to the Director of Facilities & Engineering.

This is a 100% onsite role with standard M-F hours. Responsibilities include preparing project reports, managing invoices and vendor contracts, and ensuring control documentation such as

Qualifications

  • 2+ years of experience managing engineering projects supporting process, laboratory, or facility equipment.
  • Strong technical writing ability to clearly communicate technical ideas and concepts.
  • Effective interpersonal and communication skills, both written and oral.
  • Ability to work to targets and deadlines with strong planning and organizational skills.

Responsibilities

  • Assist in preparing regularly scheduled project reports and manage invoices and purchase orders for capital projects and operational budgets.
  • Follow up on execution and review of Deviations, SOPs, and Change Controls to ensure timely completion.
  • Schedule and manage multiple engineering projects across sites using project tracking software.
  • Coordinate with schedulers and stakeholders to maintain timelines and reduce downtime.
  • Prepare and maintain detailed project schedules with milestones for oversight and communication.

Skills

Engineering project management
Technical writing
Communication skills
English proficiency
Team collaboration

Education

Bachelor’s degree in Engineering

Tools

Project tracking software

Job description

Catalent Pharma Solutions in Harmans, MD is seeking a Senior Project Engineer to lead capital projects in a GMP environment. You will coordinate scheduling, documentation, and cross‑department communication to ensure compliance and successful execution, reporting to the Director of Facilities & Engineering.

This is a 100% onsite role with standard M-F hours. Responsibilities include preparing project reports, managing invoices and vendor contracts, and ensuring control documentation such as

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