Pharma Project Coordinator - GMP, Site Logistics & Docs

Inteldot

Gurabo (PR)

On-site

USD 45,000 - 65,000

Full time

14 days+

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Job summary

Inteldot is seeking a Project Coordinator in Gurabo, Puerto Rico, to provide administrative and coordination support to capital project teams within a pharmaceutical manufacturing environment. Key responsibilities include document management, tracking project actions, and coordinating project logistics.

The ideal candidate will have a relevant technical degree and at least one year of project coordination experience. Bilingual in Spanish and English is required. This is a full-time onsite role, ensuring compliance with GMP and safety standards.

Qualifications

  • Minimum one year of project coordination experience in a regulated industry.
  • Experience supporting capital projects in pharmaceutical or biotechnology.
  • Familiarity with project documentation and procurement processes.

Responsibilities

  • Provide administrative and coordination support to project management.
  • Prepare meeting minutes, track actions, and maintain logs.
  • Support document control activities and site logistics coordination.
  • Assist in preparation of procurement packages and RFIs.
  • Facilitate communication between contractors and internal teams.

Skills

Organizational skills
Communication skills
Administrative skills
Bilingual (Spanish and English)

Education

Relevant technical diploma or degree in Engineering, Construction Management, Business Administration

Job description

Inteldot is seeking a Project Coordinator in Gurabo, Puerto Rico, to provide administrative and coordination support to capital project teams within a pharmaceutical manufacturing environment. Key responsibilities include document management, tracking project actions, and coordinating project logistics.

The ideal candidate will have a relevant technical degree and at least one year of project coordination experience. Bilingual in Spanish and English is required. This is a full-time onsite role, ensuring compliance with GMP and safety standards.

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