Unknown Company

Pharmaceutical Project Manager

houston, tx • Posted 1 weeks ago
Onsite Contract Bio & Pharmacology & Health

Build your best future with the Johnson Controls team!


As a global leader in smart, healthy, and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places, and the planet.Join a winning team that enables you to build your best future!


What we offer



  • Competitive base salary and a comprehensive bonus program.


  • Three weeks paid vacation in a calendar year / holidays / sick time / three PTO days in a calendar year.


  • Comprehensive benefits package including 401K, medical, dental, and vision care - Available day one.


  • Extensive product and on the 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)



Check us Out: A Day in the Life at JCI!


Summary: This role is the day-to-day project lead for validated environment and laboratory construction projects (e.g., cleanrooms, 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 on-site 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; elevate 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 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; portfolio responsibility not required).

  • 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 communication skills; ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.

  • Ability to lead and coordinate cross-functional teams (Owners, Architects, Engineers, QA/Validation, Contractors) in regulated contexts.

  • Proficiency with standard project management tools (Primavera P6, MS Project) and reporting platforms; advanced skills in MS Office with the ability to create executive-level dashboards and presentations.

  • Working knowledge of validation concepts, commissioning/qualification processes, data integrity best practices, and regulatory expectations for validated facilities.

  • Ability to establish and maintain professional relationships with key stakeholders and subcontractors in validated environments.

  • Willingness to travel and operate across multiple sites as needed.


Preferred:



  • Master’s degree.

  • PMI certification (PMP) or equivalent.

  • Certifications or hands‑on experience in CQV; CSV awareness; familiarity with FDA 21 CFR Part 11, EU Annex 11, and related regulatory frameworks.

  • Specific experience delivering validated environments: GMP/GLP labs, ISO 14644 cleanrooms, ISO 17025 laboratories, or similar.

  • Experience working on programs in datacenter‑adjacent facilities requiring stringent validation regimes.

  • Demonstrated ability to contribute to continuous improvement programs for validation processes and data integrity across a project portfolio.


Reporting line:



  • This position reports to the Project Executive. May supervise project coordinators or junior project team members as part of the assigned project team.


HIRING SALARY RANGE:


$130,000.00 - 165,000.00 USD Annual. (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.) This position includes a competitive benefits package.


For details, please visit the About Us tab on the Johnson Controls Careers site.


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Pharmaceutical Project Manager in houston at Unknown Company

This position is listed as contract and onsite.

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