Onsite Pharma Project Manager — GMP & Capital Projects

Inteldot; Juncos (PR); On-site; USD 90,000 - 120,000; Full time

Job summary

Inteldot, a life sciences partner with operations in Puerto Rico and the US, seeks an experienced Project Manager to lead capital projects, process improvements, and validation initiatives in a pharmaceutical manufacturing setting. You will manage scope, schedule, and budget while ensuring GMP and regulatory compliance.

The role is full-time and onsite in Puerto Rico, requiring 8+ years of PM experience in regulated industries and a Bachelor’s in engineering; bilingual in Spanish and English is

Qualifications

• Bachelor's degree in engineering required.
• 8+ years PM experience in pharmaceutical/regulated industries.
• Knowledge of GMP and regulatory requirements.

Responsibilities

• Lead project delivery across low to high complexity capital projects.
• Develop and maintain project plans, schedules, budgets, and risk registers.
• Coordinate cross-functional teams across engineering, manufacturing, packaging, and operations.
• Ensure compliance with GMP, EHSS, FDA, EMA, and regulatory requirements.
• Escalate issues and drive timely decision-making.
• Support project closeout, documentation, and lessons learned.

Skills

Leadership

Communication

Stakeholder management

Problem solving

Project planning

Education

Bachelor's degree in engineering

Job description

Inteldot, a life sciences partner with operations in Puerto Rico and the US, seeks an experienced Project Manager to lead capital projects, process improvements, and validation initiatives in a pharmaceutical manufacturing setting. You will manage scope, schedule, and budget while ensuring GMP and regulatory compliance.

The role is full-time and onsite in Puerto Rico, requiring 8+ years of PM experience in regulated industries and a Bachelor’s in engineering; bilingual in Spanish and English is