Pharma Program Manager — Parenteral Manufacturing (Onsite)

Loxo; Puerto Rico; On-site; USD 90,000 - 140,000; Full time

Job summary

Loxo is seeking a senior Program/Project Manager for a pharmaceutical/biologics manufacturing environment, located north of Puerto Rico. The role requires supervising complex, multidisciplinary projects supporting site operations, infrastructure, planning, and continuous improvement.

You will be accountable for schedule, budget, risk, stakeholder coordination, procurement support, documentation, and reporting.

Qualifications

• Must have proven PM experience in pharma/biologics manufacturing under cGMP.
• Strong communication and coordination skills in English and Spanish.

Responsibilities

• Provide overall project governance (schedule, budget, risk, resources).
• Develop and maintain integrated project schedules and milestone plans.
• Coordinate activities across Engineering, Operations, Quality, EHS, Facilities, Finance, Procurement and others.
• Support cost estimation, budgeting, and capital project planning.
• Manage procurement, coordination with vendors and engineering firms.
• Maintain risk registers and mitigation plans; manage change control and documentation.
• Coordinate regulatory and permitting activities as applicable.
• Prepare regular project status reports for leadership.
• Support GMP compliance, validation, and commissioning/qualification activities.

Skills

English proficiency

Spanish proficiency

Project management

Cross-functional coordination

Education

PMP/CCM certification

Job description

Loxo is seeking a senior Program/Project Manager for a pharmaceutical/biologics manufacturing environment, located north of Puerto Rico. The role requires supervising complex, multidisciplinary projects supporting site operations, infrastructure, planning, and continuous improvement.

You will be accountable for schedule, budget, risk, stakeholder coordination, procurement support, documentation, and reporting.