Site Integration Project Manager

PACIV

Alamogordo, NMJobNo compensation foundTracked 1mo agoSeen in employer's feed 5 days ago

Evaluate my fit

Most applications go out cold — see where you stand first. No sign-up to start.

Don't just apply. Show up ready.

Olive works from this exact posting — no sign-up to start.

Evaluate your fitSee where you stand — strengths, gaps, and what to fix first.Get started →Tailor your résuméRewritten against this posting, with a diff of every change.Get started →Practice the interviewA voice mock interview built from this job description.Get started →

At a glance

Compensation

No compensation found

Location

Alamogordo, NM

Work Authorization

Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

PACIV is hiring a Site Integration Project Manager. The Site Integration Project Manager will lead the planning and execution of projects connecting new facilities to existing pharmaceutical manufacturing operations. This role involves managing utility tie-ins, facility modifications, and other site integration projects while minimizing impact on ongoing GMP production. The manager will coordinate project scope, budget, schedule, and risks, ensuring successful completion with minimal disruption to plant operations.

Key focus areas include Manage a portfolio of site integration and utility tie-in projects from planning through turnover., Coordinate project scope, budget, schedule, contractor performance, and project risks., and Partner with Operations to plan shutdowns, production impacts, and change control activities..

Successful candidates bring Bachelor's Degree In Mechanical, Chemical, Civil Engineering, Construction Management Or Related Field, 12+ Years Capital Project Experience, and 5+ Years Managing Brownfield Or Utility Tie‑In Projects In Pharmaceutical, Biotechnology Or Chemical Manufacturing Facilities. Important skills include GMP Change Control, Management Of Change (MOC) Processes, English, and Spanish. Preferred (not required): Leadership, Communication, Stakeholder Management, and Coordinate Cross-Functional Teams.

Skills & qualifications

RequiredNice to have

Skills

GMP Change ControlManagement of Change (MOC) ProcessesEnglishSpanishLeadershipCommunicationStakeholder ManagementCoordinate Cross-Functional TeamsCoordinate ContractorsCoordinate Operations PersonnelUtility Systems KnowledgeFacility Modifications KnowledgeBrownfield Construction PracticesConstruction SafetyGMP ComplianceProject ControlsPlanningOrganizationProblem-Solving

Qualifications

Bachelor's Degree in Mechanical EngineeringBachelor's Degree in Construction ManagementBachelor's Degree in Related Field12+ Years Capital Project Experience5+ Years Managing Brownfield Projects5+ Years Managing Utility Tie-in ProjectsExperience in Pharmaceutical Manufacturing FacilitiesExperience in Biotechnology Manufacturing FacilitiesExperience in Chemical Manufacturing FacilitiesExperience in Operating GMP Manufacturing EnvironmentsProven Experience Delivering Projects Without Disrupting OperationsExperience Serving as Owner's Representative

Full job description

PACIV , a global leader in industrial automation solutions servicing the Life Sciences sector, is seeking a Site Integration Project Manager to lead the planning and execution of projects that connect new facilities to existing pharmaceutical manufacturing operations. This role is responsible for managing utility tie-ins, modifications to existing facilities, and other site integration projects while minimizing impacts to ongoing GMP production.

Position Responsibilities / Essential Functions:

Manage a portfolio of site integration and utility tie-in projects from planning through turnover.
Coordinate project scope, budget, schedule, contractor performance, and project risks.
Partner with Operations to plan shutdowns, production impacts, and change control activities.
Coordinate utility tie-ins and modifications with engineering, construction, and operations teams.
Lead contractor activities in operating facilities, including site access, training, GMP requirements, and restricted area compliance.
Promote safe execution and ensure compliance with GMP, HSE, and Management of Change (MOC) requirements.
Monitor project progress, costs, schedules, and risks, providing regular updates to project stakeholders.
Ensure successful project completion with minimal disruption to plant operations.

Requirements:

Bachelor's degree in Mechanical, Chemical, Civil Engineering, Construction Management, or a related field.
12+ years of capital project experience, including at least 5 years managing brownfield or utility tie-in projects in pharmaceutical, biotechnology, or chemical manufacturing facilities.
Experience working in operating GMP manufacturing environments.
Strong knowledge of GMP change control and Management of Change (MOC) processes.
Proven experience delivering projects without disrupting ongoing plant operations.
English required; Spanish strongly preferred.

Desired Skills:

Strong leadership, communication, and stakeholder management skills.
Experience serving as an Owner's Representative on pharmaceutical capital projects.
Ability to coordinate cross-functional teams, contractors, and operations personnel.
Knowledge of utility systems, facility modifications, and brownfield construction practices.
Strong understanding of construction safety, GMP compliance, and project controls.
Excellent planning, organization, and problem-solving skills in active manufacturing environments.

You've read the whole posting — now see how you match it.

Evaluate my fit