Scheduler/Planning Engineer

Inteldot; San Juan (PR); Hybrid; USD 70.000 - 95.000; Vollzeit

Zusammenfassung

Inteldot in Puerto Rico seeks a Scheduler / Planning Engineer to develop, maintain, and analyze detailed project schedules for capital projects in a GMP-regulated pharmaceutical environment. This role ensures accurate planning, progress tracking, and schedule performance reporting to support on-time, compliant project execution.

Candidates should have a technical degree, 1+ year scheduling experience, CPM and Primavera P6 familiarity, and strong analytical/communication skills; bilingual

Qualifikationen

• Technical degree in Engineering, Construction Management, or related field.
• Minimum 1 year scheduling experience in a regulated industry.
• Experience in scheduling/planning within capital projects, preferably pharma/regulated.
• Familiarity with scheduling tools (e.g., Primavera P6).
• Understanding of CPM and project planning principles.
• Strong analytical and communication skills.
• Bilingual in Spanish and English.

Aufgaben

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

Kenntnisse

Scheduling

CPM

Analytical thinking

Communication

Bilingual Spanish/English

Ausbildung

Engineering

Construction Management

Tools

Primavera P6

Jobbeschreibung

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.