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Pharmaceutical Project Manager

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Johnson Controls, Inc.
Full Time position
Listed on 2026-07-02
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90500 - 135000 USD Yearly USD 90500.00 135000.00 YEAR
Job Description & How to Apply Below
Location: Indianapolis

What we offer

  • Competitive base salary and a comprehensive bonus program.
  • Three weeks paid vacation a calendar year.
  • Comprehensive benefits package including 401K, medical, dental, and vision care –
    available day one
    .
  • Extensive product and job‑cross training opportunities.
  • Encouraging and collaborative team environment
    .
  • Dedication to safety through our Zero Harm policy
    .
  • Providing scheduling and management support.
  • JCI Employee discount programs (The Loop by Perk Spot).
Summary

This role is the day‑to‑day project lead for validated environment and laboratory construction projects (e.g., clean rooms, biosafety cabinets, containment suites, biocontainment labs, and related utilities) across a campus. The Project Manager will report to the Project Executive and partner with Engineering, QA/Validation, Delivery, Sponsors, and regional leadership to deliver projects within a validated‑state framework, focusing on operational excellence, compliance, and both tactical and financial performance.

What

will you do
  • Plan, execute, monitor, and close validated environment projects across multiple sites, ensuring IQ/OQ/PQ, equipment qualification, data integrity, and regulatory expectations are met.
  • Serve as the on‑site/day‑to‑day project lead, coordinating Owners, Architects, Engineers, QA/Validation, Contractors, and Vendors to achieve project objectives within validated‑state constraints.
  • Collaborate with the Project Executive to define and maintain project scope, schedule, and budget baselines; monitor progress and report deviations. Drive project schedule with a sense of urgency while not compromising quality.
  • Develop and implement validation strategies and documentation (validation plans, commissioning/qualification activities, and related records) aligned with corporate validation policy.
  • Identify, assess, and mitigate project‑level risks that could impact deliverables, schedules, budgets, data integrity, or compliance; and escalating as needed with proposed remedies.
  • Track and report project performance to the Project Executive, including schedule status, budget, risk, QA/validation progress, and regulatory readiness.
  • Manage and appropriately document change orders, project delays, procurement, and contract administration for assigned projects; ensure alignment with validated baselines and contract requirements. Update all logs on at least a weekly basis. Manage all documentation as per standards in Solution Navigator.
  • Ensure robust documentation controls that meet contract, QA, and regulatory standards (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections.
  • Seek opportunities to improve validation workflows, data integrity practices, and delivery quality to enhance client satisfaction.
  • Maintain relationships with sponsors and stakeholders; act as a trusted advisor on validated‑environment delivery and compliance at the project level.
  • Manage vendor and subcontractor performance for assigned projects, selecting qualified partners and ensuring alignment with timelines and objectives.
  • Manage project finances at the assignment level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with project baselines.
  • Prepare the project team for regulatory inspections and audits through thorough documentation and traceability.
  • Foster a safe, compliant, and collaborative project environment; provide guidance to junior team members as needed.
What you will need to be successful (Required)
  • Bachelor’s degree in Construction, Civil, Mechanical, Electrical Engineering, Construction Management, Business Management, Architecture, or a related field.
  • 5–10 years of direct project management experience on large capital projects, including regulated or validated settings (typical project sizes in the $5–$20M range).
  • Demonstrated success delivering complex, multi‑site projects in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
  • Understanding of contract language, project accounting, and basic portfolio management as they apply to validated environments.
  • Strong executive…
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