Senior Project Engineer - GMP Biotech Facility (Onsite)

Catalent Pharma Solutions; Maryland; On-site; USD 94,000 - 128,000; Full time

Benefits offered by this job

Medical, dental and vision benefits

Tuition reimbursement

PTO + 8 holidays

Job summary

Catalent's Harmans, MD facility is seeking a Senior Project Engineer to lead engineering projects in an FDA-regulated environment. You will coordinate scheduling, documentation, and cross-functional communication with internal teams and external vendors to ensure compliance and successful execution.

The role reports to the Director, Facilities & Engineering and involves preparing project reports, managing budgets, and applying GMP-related standards.

Qualifications

• Bachelor’s degree in Engineering or related field.
• 4 years of experience managing engineering projects in pharma/biotech settings.
• Strong technical writing and clear communication skills.
• Ability to work to targets and deadlines with planning and organization.
• English proficiency required.

Responsibilities

• Prepare regularly scheduled project reports.
• Manage invoices and purchase orders for capital projects.
• Review deviations, SOPs, and change controls to ensure timely completion.
• Maintain detailed project schedules and milestones.
• Coordinate with schedulers and stakeholders to meet timelines.
• Lead cross-functional teams to deliver project deliverables.

Skills

Project management

Communication

Planning

English (written)

Education

Bachelor's degree in Engineering

Tools

Project tracking software

Job description

Catalent's Harmans, MD facility is seeking a Senior Project Engineer to lead engineering projects in an FDA-regulated environment. You will coordinate scheduling, documentation, and cross-functional communication with internal teams and external vendors to ensure compliance and successful execution.

The role reports to the Director, Facilities & Engineering and involves preparing project reports, managing budgets, and applying GMP-related standards.