Unleash your potential 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 our winning team and pave the way for a bright future. With our extensive reach across various industries worldwide, our teams are uniquely positioned to support and empower you. You will have the opportunity to develop yourself through meaningful work projects and learning opportunities. We strive to provide our employees with an experience focused on supporting their physical, financial, and emotional wellbeing.
Join the Johnson Controls family and thrive in a culture that values your voice and ideas.
Your next incredible opportunity is just a few clicks away!
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 Life at JCI!
What will you do:
Provide executive-level leadership for a portfolio of validated environment and laboratory construction programs (including cleanrooms, BSCs, containment suites, biocontainment labs, and associated utilities) across a campus.
Act as the domain authority for programs requiring rigorous validation lifecycles (IQ/OQ/PQ), equipment qualification, and compliant deployment of regulated systems, ensuring alignment with corporate validation strategy and regulatory expectations.
Set strategic direction and governance for the validated program portfolio, partnering with QA/Validation, Project Development, Delivery, Sponsors, and regional leadership to achieve objective outcomes within a validated-state framework.
Lead the campus Project Management Office for validated environments, ensuring compliance with contract requirements, validation plans, and data integrity standards while coordinating with enterprise systems for performance reporting.
Anticipate, escalate, and mitigate risks that could impact validation deliverables, schedules, budgets, data integrity, or regulatory compliance; drive issues to resolution with executive-level visibility.
Oversee risk management of the campus portfolio, directing recovery and remediation plans that preserve validated status and impact metrics (scope, schedule, cost, quality).
Ensure accurate, timely, and actionable reporting of portfolio performance to Executive Management, including financial performance, validation milestones, compliance status, and risk controls, using validated data sources and enterprise systems.
Drive client relationship management and business development within the validated-environment sector, identifying opportunities to expand scope, deepen partnerships, and improve customer satisfaction through compliant, high-quality delivery.
Lead strategic vendor and subcontractor relationships, selecting qualified partners experienced in validated environments and aligning them to project goals and timelines.
Govern program financials at the campus level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with validated project baselines.
Ensure program documentation controls meet contract, regulatory, and QA requirements (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections/audits.
Continually seek opportunities to improve client satisfaction, streamline validation workflows, and enhance the competitive position through compliant, high-quality delivery.
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.
15+ years of direct Project/Program Management experience, including large, capital projects in regulated or validated settings (minimum $10M per project; portfolio-level responsibility preferred).
Demonstrated success delivering complex, multi-site programs in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
Deep understanding of contract language, project accounting, and portfolio management as they apply to validated environments.
Strong executive communication skills, with proven ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
Proven ability to lead and align diverse, 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 leading programs in datacenter-adjacent facilities requiring stringent validation regimes.
Demonstrated ability to develop and implement continuous improvement programs for validation processes and data integrity across a portfolio.
HIRING SALARY RANGE: $105,000.00 - 145,000.00 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.
Job Role – Senior Executive About the Organisation You will be joining a global life sciences and pharmaceutical organisation within Inizio Ignite , working across two highly specialised divisions— STEM Healthcare and Research Partnership . Together, these teams deliver strategic insights, benchmarking, market research, ...
... delivery across initiation, planning, execution, monitoring, and closure, using the methodology and tools appropriate to each initiative. - Develop and maintain project governance artifacts, including project plans, scope, milestones, dependencies, resource plans, risks, issues, releases, and deliverables. - Proactively manage ...
... generated total revenues of EUR € 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Job Title: IAM Project & Governance Manager Shift Timing: 12PM to 9PM Reporting to: Senior Manager Work Location: Bangalore, India SUMMARY OF ROLE AND OBJECTIVES: The IAM Project ...
... certifications in project coordination, administration, operations, or communication will be an advantage. Required Experience - 1–2 years of experience as an Executive Assistant, Founder’s Office Executive, Operations Coordinator, Program Coordinator, or a similar role. - Prior experience supporting founders, CXOs, senior ...
... operating models can transform the pharmaceutical and life sciences value chain from discovery through commercialization and market access. Key Responsibilities Executive Client Engagement - Lead and facilitate executive-level CFR visits for pharmaceutical, biotech, medtech, and healthcare clients and internal EY senior stakeholders ...
... schedules, risk registers, and governance routines - Coordinate cross-functional dependencies across engineering, product, data, and business teams - Produce executive-ready status reports, dashboards, and decision briefings - Mentor less experienced project managers on planning and stakeholder communication Requirements ...
... (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors. - Deep understanding of contract language, project accounting, and portfolio management as they apply to validated environments. - Strong executive communication skills, with proven ability to present to senior ...
... within assigned projects using SAS and other proprietary software.- Demonstrates judgment in resolving problems.- Maintain quality and timeliness of assigned project activities and perform control checks with help of other team members for all the generated reports.- Work with the programming teams and projects to ensure ...
... within assigned projects using SAS and other proprietary software.- Demonstrates judgment in resolving problems.- Maintain quality and timeliness of assigned project activities and perform control checks with help of other team members for all the generated reports.- Work with the programming teams and projects to ensure ...
Job Title: IT Helpdesk Support Specialist - Laboratory IT (Pharmaceutical Manufacturing) Overview: We are seeking an experienced IT Helpdesk Support Specialist to join our team and provide technical assistance for Laboratory IT systems in pharmaceutical manufacturing. The ideal candidate will have expertise in IT support, ...