Endo International plc

Project Engineer

Endo International plc$83K — $113K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

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)
  • Strong project management and organizational skills
  • Excellent communication and stakeholder management abilities

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.

Benefits

  • Support for continuous improvement initiatives and professional development activities.
  • Opportunity to participate in cross-functional projects and training sessions.
  • Access to maintaining departmental documentation and process optimization efforts.
  • Work in a diverse environment balancing office work and manufacturing plant activities.
  • Regular opportunities for interdepartmental coordination and teamwork.
Full Job Description
Job Description Summary

The Project Engineer is responsible for managing and executing capital expenditure projects within a pharmaceutical manufacturing environment. This role ensures projects are delivered safely, on time, within budget, and in compliance with regulatory standards (GMP, FDA, etc.).

Job Description

ESSENTAIL FUNCTIONS:
• 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.

DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
• Perform additional duties and special projects as assigned by department leadership.
• Support continuous improvement initiatives within the department.
• Assist with cross-functional projects and interdepartmental coordination.
• Participate in training sessions, workshops, and professional development activities.
• Maintain departmental documentation, reports, and records as required.
• Provide backup support for other team members during absences or peak workloads.
• Contribute to process optimization and efficiency improvements.
• Attend meetings and provide input on departmental goals and performance.
• Support implementation of new tools, systems, or procedures within the department.
• Ensure compliance with company policies and relevant regulatory requirements when performing assigned tasks.

MINIMUM REQUIREMENTS:

Education:
Bachelor's Degree in Engineering (Chemical, Mechanical, Electrical or related discipline)

Experience:
1-3+ years experience in manufacturing environments. (Pharmaceutical or regulated manufacturing preferred)

Preferred Skills/Qualifications:
• Proven experience managing CAPEX projects.
• Strong knowledge of GMP and regulatory requirements.
• Project Management certification (PMP or equivalent )

Other Skills:
• Strong project management and organizational skills.
• Excellent communication and stakeholder management abilities.
• Technical expertise in process equipment and facility systems.
• Problem-solving mindset with attention to detail.
• Ability to manage multiple projects simultaneously.

Competencies:
• CAD/CAM Proficiency
• Problem Solving & Root Cause Analys
• Continuous Improvement (Lean/Six Sigma)
• Automation & Industry 4.0 Awareness

WORKING CONDITIONS:
• Position will work both an office environment and in a manufacturing plant environment.
• Must be able to wear the required Personal Protective Equipment (PPE) out on the plant site as deemed necessary by EH&S.
• Occasional travel required.

The expected base pay range for this position is $83,895 -$113,505. Please note that base pay offered may vary depending on factors including job-related knowledge, skills, and experience.

About Endo International plc

Endo International plc is a global specialty pharmaceutical company focused on improving patients' lives while creating shareholder value. Endo develops, manufactures, markets and distributes quality branded and generic pharmaceutical and non-pharmaceutical products. The Company operates through three segments: U.S. Branded Pharmaceuticals, U.S. Generic Pharmaceuticals and International Pharmaceuticals. Endo's headquarters are in Dublin, Ireland, and its operational headquarters are in Malvern, Pennsylvania, USA. Endo has global headquarters in Dublin, Ireland, and U.S. headquarters in Malvern, Pennsylvania. The Company's ordinary shares are listed on the NASDAQ Global Select Market under the symbol ENDP.
Learn more about Endo International plc
Size
3,103 employees
Market Cap
$68.3 million
Industry
Net Income
$183.9 million
5 Year Trend
-5.7%
Revenue
$2.9 billion
NASDAQ

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