Project Manager | Pharmaceutical Manufacturing

Job DescriptionJob DescriptionLocation: Gurabo, Puerto Rico (On Site) Industry: Pharmaceutical Manufacturing – Solid Dosage Position Type: ContractPosition OverviewWe 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.Main 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.General Requirements: Fluent in English (spoken and written).Proficiency in Microsoft Office 365 (Teams, SharePoint, Outlook, Excel, Word, PowerPoint) and project management tools.PMP or LPP certification (preferred).Excellent communication and leadership skills.Attention to detail, excellent problem solving and organizational skills.Strong understanding of pharmaceutical manufacturing environments.Knowledge of solid dosage manufacturing processes preferred.Education Requirements: Bachelor’s Degree in industrial engineering or other related fields.Master's Degree in Management, Project Management, Engineering or a related field (a plus).Experience Requirements: Minimum of 3 years of Project Management experience within the pharmaceutical industry preferred.Proficiency in project management tools.5+ years of process improvement experienceExperience supporting projects in solid dosage manufacturing environments is highly preferred.Physical Requirements: Ability to sit for long periods.Light physical activity may be required occasionally.Must be able to visit field locations as needed.Must be able to use personal protective equipment (PPE) when required.Ability to perform in a variety of industrial environments.