Project Manager (s) - East PR region

Integrated Services for Productivity & Validation, Inc

Canóvanas (PR)

On-site

USD 100,000 - 130,000

Full time

14 days+

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Job summary

A leading service provider in the pharmaceutical industry is seeking an experienced project manager to oversee complex facility projects in Canóvanas, Puerto Rico. The ideal candidate will have a Bachelor's degree in Engineering and over 10 years of project management experience in the pharmaceutical industry. Responsibilities include managing stakeholders, controlling costs, and driving critical installations from design to commissioning. This position offers an opportunity to work with cutting-edge technology while ensuring quality and adherence to industry standards.

Qualifications

  • Must have 10+ years of experience managing pharmaceutical industry projects.
  • Experience overseeing complex facility projects is required.
  • Must ensure adherence to quality, budget, and schedule requirements.

Responsibilities

  • Oversee planning and execution of facility projects from design to commissioning.
  • Manage project stakeholders including architects and contractors.
  • Control costs and coordinate site activities related to project execution.

Skills

Project management
Knowledge of GMP and OSHA
Stakeholder management
Cost control
System installations

Education

Engineering Bachelor's Degree

Job description

Integrated Services For Productivity & Validation, Inc | Contract

Canovanas, Puerto Rico | Posted on 01/21/2026

We provide the industry with a platform of solutions designed to their actual needs. We share and implement leading edge technology and methods that exceed customer expectation and deliver a one-stop provider of services focus on the well-being of the company and the employees.

Job Description

Qualified / Available contractors must have vast experience managing pharmaceutical projects.

Oversees the planning, execution, and closeout of complex facility projects (labs, manufacturing, etc.), ensuring strict adherence to GMP , safety (OSHA), quality, budget, and schedule, by managing stakeholders (architects, engineers, contractors), controlling costs, coordinating site activities, handling permits, and driving critical system installations (HVAC, clean utilities) from design to commissioning .

Requirements

Must have an Engineering Bachelors Degree, 10 plus years of Project management experience with Pharmaceutical Industry projects related to equipment and/or manufacturing processes.

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