Program Manager – GMP Facilities, On-Site Lead

Validation & Engineering Group, Inc.; Manatí (PR); On-site; USD 120,000 - 160,000; Full time

Job summary

Validation & Engineering Group, Inc. seeks a Program/Project Manager to lead complex pharma/biologics projects on-site in a multi-workstream environment.

You will own schedules, budgets, risk, and stakeholder communications, coordinating with Engineering, Operations, Quality, EHS, and Facilities to ensure GMP alignment and timely delivery. Ideal candidates bring experience managing CHP/SMP type programs, a track record in site master planning, and relevant certifications.

Qualifications

• Proven PM experience in pharma/biologics facilities operating under cGMP.
• Direct experience leading site master planning engagements at industrial/life sciences campuses.
• Certifications like PMP/CCM are preferred for lead roles.

Responsibilities

• Govern overall program and project schedule, budget, and risk.
• Coordinate stakeholders across Engineering, Ops, Quality, EHS, Facilities, Finance, Procurement.
• Develop and maintain integrated master schedules and cost tracking.

Skills

Leadership

Stakeholder management

Budget management

GMP/CGMP knowledge

Bilingual English/Spanish

Education

Engineering degree

Tools

MS Project

Primavera

Job description

Validation & Engineering Group, Inc. seeks a Program/Project Manager to lead complex pharma/biologics projects on-site in a multi-workstream environment.

You will own schedules, budgets, risk, and stakeholder communications, coordinating with Engineering, Operations, Quality, EHS, and Facilities to ensure GMP alignment and timely delivery. Ideal candidates bring experience managing CHP/SMP type programs, a track record in site master planning, and relevant certifications.