Position Responsibilities / Essential Functions:
- Manage an assigned construction package, including scope, budget, schedule, contracts, and project risks.
- Lead contractor execution from mobilization through mechanical completion and system turnover.
- Coordinate with design, construction, and equipment teams to resolve RFIs, design changes, and field issues.
- Monitor contractor performance and ensure work is completed safely, on schedule, and to quality standards.
- Support GMP-compliant construction practices and minimize rework on critical systems.
- Promote a strong safety culture and ensure compliance with project HSE requirements.
- Manage project change control, contractor claims, and monthly cost and schedule reporting.
- Coordinate system turnover activities with Commissioning & Qualification (C&Q) teams.
- Collaborate with other Project Managers and stakeholders to ensure seamless project execution.
- Bachelor's degree in Civil, Mechanical, Electrical, Chemical, Construction Engineering, or a related field.
- 15+ years of capital project experience, including at least 7 years managing pharmaceutical or biotechnology facility construction projects.
- Experience managing large-scale construction projects ($100M+ preferred).
- Experience with cleanroom, GMP, or pharmaceutical manufacturing facilities.
- Strong contractor management, change management, and project controls experience.
- PMP certification and OSHA 30 certification preferred.
- English required; Spanish strongly preferred.
- Strong leadership, communication, and stakeholder management skills.
- Experience serving as an Owner's Representative on large capital projects.
- Ability to manage multiple contractors and cross-functional project teams.
- Knowledge of GMP regulations and pharmaceutical construction standards.
- Experience in one or more of the following disciplines:
- Civil, Structural, and Architectural (CSA)
- Mechanical, Electrical, and Plumbing (MEP) Fit-Out
- Process and Clean Utilities
- Strong problem-solving, planning, and organizational skills with the ability to deliver projects safely, on time, and within budget.
Skills Required
- Bachelor's degree in Civil, Mechanical, Electrical, Chemical, Construction Engineering, or related field
- 15+ years of capital project experience
- At least 7 years managing pharmaceutical or biotechnology facility construction projects
- Experience with cleanroom, GMP, or pharmaceutical manufacturing facilities
- Strong contractor management, change management, and project controls experience
- Ability to manage multiple contractors and cross-functional project teams
- Experience managing large-scale construction projects ($100M+)
- PMP certification
- OSHA 30 certification
- English language proficiency
- Spanish language proficiency
- Experience serving as an Owner's Representative on large capital projects
- Knowledge of GMP regulations and pharmaceutical construction standards
- Experience in Civil/Structural/Architectural (CSA), MEP fit-out, or Process and Clean Utilities disciplines
- Strong leadership, communication, problem-solving, planning, and organizational skills
What We Do
PACIV, Inc. (Process Automation – Controls.Instruments.Validations) was founded and registered as a corporation in the Commonwealth of Puerto Rico in 1997. Listening to our clients' desire for local support and standardization among their facilities, we opened our Indiana office (PACIV-USA, LLC) in 2003. Moreover, in 2011 we opened PACIV-Ireland in Cork, Ireland. Our expansion, including international presence with local resources, responds to the needs of our Life Sciences multinational clients regarding replication and consistency of implementation, who demand our life sciences automation and regulatory compliance solutions in a localized market format. Our thorough understanding of the challenges faced by the Life Science sector and our collaborative approach with our clients has enabled us to become a leading Life Sciences automation and regulatory compliance service company. Since our inception, we provide our Life Sciences clients with our services in their multiple manufacturing sites worldwide. The fact that we hold Master Service Agreements (MSA’s) and Preferred Vendor status with the world’s leading Life Science Companies serves a testimony of our quality of service and leadership standing within the Life Science industry. We attract and develop the best talent which allows us to provide our demanding clients with the right knowledge and expertise ensuring we provide significant value within our automation solutions and services.
