Pharma CAPEX Project Engineer

Endo; Hobart (IN); On-site; USD 84,000 - 114,000; Full time

Job summary

Par Health in the United States is seeking a Project Engineer to lead end-to-end CAPEX projects in a pharmaceutical manufacturing environment, delivering projects safely, on time, and within budget while complying with GMP and FDA requirements.

The role requires a Bachelor's in Engineering, 1–3+ years in pharma manufacturing, PMP or equivalent, and strong skills in project management, coordination with cross-functional teams, and documentation.

Qualifications

• Bachelor’s degree in Engineering (Chemical, Mechanical, Electrical or related discipline).
• 1–3+ years experience in manufacturing environments; pharmaceutical or regulated manufacturing preferred.
• Proven experience managing CAPEX projects.
• Strong knowledge of GMP and regulatory requirements.
• Project Management certification (PMP or equivalent).

Responsibilities

• Lead end-to-end execution of CAPEX projects including planning, design, procurement, construction and commissioning.
• Develop project scopes, budgets, schedules, and resource plans.
• Coordinate cross-functional teams including engineering, quality, validation, manufacturing, and external vendors.
• Ensure compliance with cGMP, FDA, EMA, and other regulatory requirements.
• Oversee equipment selection, installation, and qualification (IQ/OQ/PQ).
• Manage contractors, suppliers, and construction activities on-site.
• Perform risk assessments and implement mitigation strategies.
• Track project performance and provide regular status updates to stakeholders.
• Drive continuous improvement and cost optimization in project execution.
• Ensure proper documentation and support validation efforts.

Skills

CAPEX project leadership

GMP knowledge

PMP certification

Education

Bachelor's in Engineering

Job description

Par Health in the United States is seeking a Project Engineer to lead end-to-end CAPEX projects in a pharmaceutical manufacturing environment, delivering projects safely, on time, and within budget while complying with GMP and FDA requirements.

The role requires a Bachelor's in Engineering, 1–3+ years in pharma manufacturing, PMP or equivalent, and strong skills in project management, coordination with cross-functional teams, and documentation.