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.