Onsite Pharma Project Manager — GMP & Compliance

Inteldot; Gurabo (PR); On-site; USD 90,000 - 110,000; Full time

Job summary

Inteldot is seeking a Project Manager for a full-time, onsite role in Gurabo, Puerto Rico. The role involves leading capital projects and ensuring compliance with regulatory standards in a pharmaceutical manufacturing environment.

Ideal candidates will have 8+ years of project management experience, a Bachelor's degree in engineering, and strong leadership and communication skills. Bilingual in Spanish and English is a plus.

Qualifications

• 8+ years of project management experience in pharmaceutical or regulated industries.
• Strong knowledge of GMP and regulatory compliance in a pharmaceutical environment.
• Experience managing capital projects and process improvements.

Responsibilities

• Lead overall project delivery and execution across various project complexities.
• Manage project scope, risks, and change control activities.
• Ensure compliance with GMP, EHSS, FDA, and EMA regulations.

Skills

Leadership

Communication

Stakeholder management

Problem-solving

Bilingual (Spanish and English)

Education

Bachelor's degree in engineering

Tools

Project planning and scheduling tools

Job description

Inteldot is seeking a Project Manager for a full-time, onsite role in Gurabo, Puerto Rico. The role involves leading capital projects and ensuring compliance with regulatory standards in a pharmaceutical manufacturing environment.

Ideal candidates will have 8+ years of project management experience, a Bachelor's degree in engineering, and strong leadership and communication skills. Bilingual in Spanish and English is a plus.