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Open nowPosted 10 days ago

Scheduler/Planning Engineer

inteldot18 open roles

Where
Juncos, Puerto Rico
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Your applicationOpen nowScheduler/Planning Engineerinteldot · Juncos, Puerto Rico

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  4. 14.6%14 days
  5. 34.1%30 days
This job: posted 10 days ago

The posting

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 Scheduler / Planning Engineer is responsible for developing, maintaining, and analyzing detailed project schedules for capital projects within a regulated pharmaceutical environment. This role ensures accurate planning, progress tracking, and schedule performance reporting to support compliant, safe, and on-time project execution aligned with GMP and company standards.

Key Responsibilities

  • Develop and maintain detailed project schedules using client approved scheduling tools.
  • Apply scheduling techniques including logic development, critical path analysis, resource leveling, and look-ahead planning.
  • Produce regular schedule updates, progress reports, and schedule performance analyses.
  • Perform schedule risk analysis and identify delays, conflicts, and dependencies across projects.
  • Coordinate with project teams to resolve scheduling issues and optimize execution sequencing.
  • Support integration and alignment of schedules across multiple capital projects.

Requirements & Qualifications

  • Relevant technical degree in Engineering, Construction Management, or related field.
  • Minimum one (1) year of scheduling experience in the regulated industry.
  • Experience in project scheduling or planning within capital projects, preferably in pharmaceutical or regulated industries.
  • Familiarity with scheduling tools (e.g., Primavera P6 or equivalent).
  • Understanding of critical path method (CPM) and project planning principles.
  • Strong analytical and communication skills.
  • Bilingual (Spanish and English).

Preferred Qualifications

  • Experience in pharmaceutical, biotechnology, or industrial construction projects.
  • Familiarity with GMP-regulated environments and project lifecycle phases (design, construction, commissioning).
  • Exposure to integrated project controls environments.
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