Project Manager | Pharmaceutical Manufacturing

LEGAL PROJECT MANAGEMENT PARTNERS LLC • Caguas, PR

2d • Onsite

About The Position

We are seeking a motivated and experienced Project Manager to support pharmaceutical manufacturing operations in a GMP-regulated environment. The ideal candidate will have hands-on experience managing projects within the pharmaceutical industry, specifically related to solid dosage manufacturing processes. This role will focus on coordinating cross-functional activities, supporting project execution, driving timelines, and ensuring projects are completed efficiently while maintaining compliance with pharmaceutical standards and procedures. The ideal candidate is someone with strong pharmaceutical process knowledge and practical project management experience. Extensive budgeting or advanced scheduling expertise is not required for this position.

Requirements

• Fluent in English (spoken and written).
• Proficiency in Microsoft Office 365 (Teams, SharePoint, Outlook, Excel, Word, PowerPoint) and project management tools.
• Excellent communication and leadership skills.
• Attention to detail, excellent problem solving and organizational skills.
• Strong understanding of pharmaceutical manufacturing environments.
• Proficiency in project management tools.
• 5+ years of process improvement experience

Nice To Haves

• PMP or LPP certification (preferred).
• Knowledge of solid dosage manufacturing processes preferred.
• Experience supporting projects in solid dosage manufacturing environments is highly preferred.

Responsibilities

• Manage and support pharmaceutical projects related to manufacturing processes, equipment, and operational improvements.
• Coordinate activities between cross-functional teams including Manufacturing, Engineering, Quality, Validation, and Operations.
• Monitor project progress, deliverables, timelines, and action items to ensure successful execution.
• Facilitate meetings, provide project updates, and communicate status to internal stakeholders.
• Support implementation of process improvements and operational initiatives within GMP environments.
• Ensure project activities comply with company procedures, safety standards, and regulatory requirements.
• Identify project risks, issues, and potential delays while helping develop mitigation plans.
• Assist with documentation review, change controls, and project-related records as needed.
• Collaborate with site personnel to ensure alignment with manufacturing priorities and business objectives.

What This Job Offers

• Career Level: Mid Level