Pharmaceutical Project Manager

Alloy Enterprises; Milwaukee (WI); On-site; USD 130,000 - 165,000; Full time

Benefits offered by this job

Competitive base salary

Three weeks paid vacation

Comprehensive benefits package

On-the-job training

Collaborative team environment

Zero Harm policy

Scheduling and management support

Employee discount programs

Job summary

Johnson Controls seeks a senior Project Manager to lead validated-environment construction projects across multiple sites, including GMP/GLP facilities. You will ensure IQ/OQ/PQ, data integrity, and regulatory readiness while coordinating Owners, Architects, Engineers, QA/Validation, and Contractors.

You will manage scope, schedule, and budgets, develop validation plans, and drive risk mitigation with a focus on quality and compliance. Willingness to travel is expected.

Qualifications

• Bachelor's degree in construction, civil, mechanical, electrical engineering, construction management, business, or related field.
• 5–10 years of direct project management on large capital projects in regulated settings (GMP/GLP/ISO 17025).
• Experience delivering multi-site validated environments in labs, pharma, or healthcare sectors.
• Knowledge of contract language, project accounting, and portfolio management for validated environments.
• Strong executive communication and stakeholder influence.

Responsibilities

• Plan, execute, monitor, and close validated environment projects across multiple sites.
• Coordinate Owners, Architects, Engineers, QA/Validation, Contractors, and Vendors to meet objectives.
• Define scope, schedule, and budget baselines; monitor progress and report deviations.
• Develop validation strategies and documentation aligned with corporate policy.
• Identify and mitigate project risks impacting deliverables, budgets, or compliance.
• Track performance and report to Project Executive; manage changes and logs weekly.
• Ensure documentation controls meet QA and regulatory standards for inspections.
• Travel to multiple sites as needed and lead cross-functional teams.

Skills

Executive communication

Cross-functional leadership

Travel willingness

Regulated environments knowledge

Education

Bachelor's degree in construction, engineering, or related field

Tools

Primavera P6

MS Project

MS Office advanced

CSV/validation awareness

Job description

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!

Our teams are uniquely positioned to support a multitude of industries across the globe. 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.

Become a member of the Johnson Controls family and thrive in an empowering company culture where your voice and ideas will be heard – your next great 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 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.

https://jobs.johnsoncontrols.com/about-us

Johnson Controls International plc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, genetic information, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. To view more information about your equal opportunity and non-discrimination rights as a candidate, visit EEO is the Law. If you are an individual with a disability and you require an accommodation during the application process, please visit here.