Project Engineer

Inteldot

Gurabo (PR)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Job summary

Inteldot is seeking a Project Engineer to support the planning and execution of capital projects within a regulated pharmaceutical manufacturing environment in Gurabo, Puerto Rico. The role involves collaborating with cross-functional teams to ensure compliance with GMP and quality standards, playing a critical part in both synthetic and biotherapeutic operations.

The ideal candidate will have a Bachelor's degree in engineering and a minimum of 3 years of experience in the pharmaceutical industry. Strong communication skills in both English and Spanish are essential for success.

Qualifications

  • Minimum 3 years of experience managing or supporting capital projects in the pharmaceutical industry.
  • Experience in manufacturing and packaging processes and equipment.
  • Familiarity with GMP environments and regulated project execution.

Responsibilities

  • Support execution of capital projects through technical engineering input.
  • Assist with technical design development and design reviews.
  • Ensure engineering deliverables comply with GMP and safety standards.

Skills

Project management
GMP compliance
Bilingual (Spanish and English)
Technical problem-solving
Communication skills

Education

Bachelor’s degree in engineering

Job description

Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Employment type: Full time and onsite role

Role Summary

The Project Engineer supports the planning, design, and execution of capital projects within a regulated pharmaceutical manufacturing environment. This role provides technical engineering support across manufacturing, packaging, equipment, and facility-related projects in both synthetic and biotherapeutic operations. The Project Engineer works closely with cross-functional teams, contractors, and vendors to ensure successful delivery of engineering solutions in compliance with GMP, safety, and quality standards.

Key Responsibilities
  • Support the execution of capital projects through technical engineering input and coordination.
  • Assist with technical design development, engineering deliverables, and design reviews.
  • Review and manage design change requests in alignment with project requirements and quality standards.
  • Liaise with engineering contractors, equipment vendors, and internal technical Subject Matter Experts (SMEs).
  • Support development of basis-of-design (BOD) documents and technical specifications.
  • Participate in installation, commissioning, and qualification activities for manufacturing and packaging systems.
  • Support punch-list development, tracking, and resolution during project execution and closeout.
  • Ensure engineering deliverables comply with GMP, safety, and regulatory requirements.
  • Assist in troubleshooting technical issues and supporting project execution timelines.
Requirements & Qualifications
  • Bachelor’s degree in engineering (Mechanical, Chemical, Electrical, or related field).
  • Minimum 3 years of experience managing or supporting capital projects in the pharmaceutical industry.
  • Experience in manufacturing and packaging processes and equipment, including synthetic and/or biotherapeutic operations.
  • Familiarity with GMP environments and regulated project execution.
  • Experience working with engineering design documentation, specifications, and construction/installation support.
  • Strong communication skills with ability to work across contractors, vendors, and internal teams.
  • Ability to support technical problem-solving and coordinate multiple stakeholders.
  • Bilingual (Spanish and English).
Preferred Qualifications
  • Experience supporting commissioning, qualification, and validation (CQV) activities.
  • Familiarity with cleanroom environments, pharmaceutical utilities, or process systems.
  • Exposure to design change control processes in regulated environments.
  • Understanding of project lifecycle from design through installation and startup.
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