Project Manager
About this RoleThis role leads the planning, execution, and delivery of construction and facility-related projects within a regulated pharmaceutical environment.Key ResponsibilitiesOversee end-to-end project lifecycle for construction, facility upgrades, utilities, and infrastructure projects within GMP environments.Develop and manage project scopes, budgets, schedules, risk registers, and change controls.Lead cross-functional coordination with Engineering, Validation, Quality, Operations, EHS, Procurement, and external contractors.Ensure all work complies with FDA, GMP, OSHA, and site-specific safety and documentation standards.Prepare and maintain project documentation: URS, design packages, commissioning plans, status reports, and closeout packages.Conduct site walks, contractor oversight, and safety audits to ensure adherence to construction and EHS protocols.Facilitate timely decision-making, escalation management, and stakeholder communication.Support commissioning, qualification, and turnover activities for new or modified systems.Drive continuous improvement in project workflows, contractor management, and communication practices.Required QualificationsBachelor's degree in Engineering (Mechanical, Electrical, Civil, Chemical, Industrial) or related field.5+ years of experience managing construction or capital projects in pharmaceutical, biotech, medical device, or similarly regulated industries.Strong understanding of GMP, EHS, and validation principles.Proven ability to manage contractors, negotiate scopes, and maintain project controls.Experience with project management tools (MS Project, Primavera, or similar).Excellent communication skills in English and Spanish, with the ability to translate technical information clearly for diverse audiences.Demonstrated ability to work in fast-paced, compliance-driven environments with multiple priorities.Preferred QualificationsExperience with cleanrooms, utilities (HVAC, WFI, compressed air), and process equipment installations.Knowledge of CQV methodologies and documentation.PMP, CAPM, or equivalent certification.Experience in Puerto Rico's pharmaceutical manufacturing ecosystem.Competencies & Work StyleStrong ownership mindset with disciplined follow-through.Clear, respectful communicator who maintains alignment across teams.Organized, detail-oriented, and proactive in identifying risks and solutions.Comfortable balancing field presence with documentation and stakeholder management.Values safety, compliance, and ethical decision-making.What's In It for YouComprehensive health coverage (medical, dental, and vision)Company-paid life and disability insuranceOptional benefits such as pet insurance, legal, and supplemental health plans401(k) with day-one eligibility, 3% safe harbor, plus up to 2.5% company matchGenerous time off: 10 paid holidays and PTO starting at 15 days, growing up to 25Access to Consertus Academy for continuous learning and developmentEqual Employment Opportunity StatementConsertus is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We welcome applicants from all backgrounds and identities, and we do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, veteran status, or any other protected status.J-18808-Ljbffr