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Pharmaceutical Project Engineer Jobs (NOW HIRING)

Johnson Controls, Inc.

The Project Manager will report to the Project Executive and partner with Engineering, QA ... biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.

The Rockridge Group

Project Engineer

Wilson, NC · On-site

Project Engineer, Pharmaceutical Packaging Line LOCATION: Wilson, NC Shift Schedule: Onsite role, no hybrid schedule. Monday-Thursday: 7:00am-5:30pm EST DURATION Feb 5 - 12/31/2024 Job Summary: The ...

Nooter Construction

Project Engineer

Lebanon, IN · On-site

The ideal Project Engineer can hit the ground running, manage multiple priorities with minimal ... You will understand complex electrical construction projects within the pharmaceutical and life ...

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Pharmaceutical Project Engineer information

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$45K

$90.6K

$136K

How much do pharmaceutical project engineer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for pharmaceutical project engineer in the United States is $90,644.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $103,500.00 per year, depending on experience, location, and employer.

What does a pharmaceutical project engineer do?

A Pharmaceutical Project Engineer is responsible for planning, coordinating, and overseeing engineering projects within pharmaceutical manufacturing or research facilities. Their work includes designing and implementing new production processes, managing equipment installations, ensuring compliance with industry regulations, and optimizing operations for efficiency and safety. They often collaborate with cross-functional teams such as quality assurance, validation, and production to make sure projects are completed on time and within budget.

How does a pharmaceutical project engineer typically collaborate with cross-functional teams during a project lifecycle?

Pharmaceutical Project Engineers work closely with cross-functional teams, including quality assurance, regulatory affairs, production, and R&D, to ensure that projects meet industry standards and compliance requirements. They often facilitate communication between departments, manage timelines, and coordinate technical solutions to address challenges that arise. This collaborative approach is key to delivering projects on time while adhering to strict safety and regulatory guidelines. Effective teamwork and communication skills are essential, as engineers must align diverse stakeholders and maintain project momentum.

What are the key skills and qualifications needed to thrive as a pharmaceutical project engineer, and why are they important?

To thrive as a Pharmaceutical Project Engineer, you need a solid background in engineering (usually a degree in chemical, mechanical, or process engineering), combined with knowledge of pharmaceutical manufacturing processes and regulatory standards. Familiarity with project management software, CAD tools, and validation protocols, along with certifications like PMP or Six Sigma, is often required. Excellent problem-solving, communication, and teamwork skills help manage cross-functional teams and address complex project challenges. These skills and qualifications are crucial to ensure projects are delivered efficiently, safely, and in compliance with industry regulations.

What is the difference between Pharmaceutical Project Engineer vs Pharmaceutical Manufacturing Specialist?

AspectPharmaceutical Project EngineerPharmaceutical Manufacturing Specialist
CredentialsBachelor's in Engineering, Project Management certificationsTechnical degree, GMP training, certifications in manufacturing processes
Work EnvironmentEngineering offices, labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical manufacturing facilities, contract manufacturers
Primary FocusPlanning, executing, and managing engineering projectsEnsuring manufacturing processes meet quality and compliance standards

The Pharmaceutical Project Engineer focuses on managing engineering projects within pharmaceutical companies, overseeing design, installation, and process improvements. In contrast, the Pharmaceutical Manufacturing Specialist concentrates on the day-to-day operations of manufacturing processes, ensuring quality and compliance. Both roles are essential in pharmaceutical production but differ in scope and responsibilities.

More about Pharmaceutical Project Engineer jobs

What states have the most Pharmaceutical Project Engineer jobs?

States with the most job openings for Pharmaceutical Project Engineer jobs include:

What are popular job titles related to Pharmaceutical Project Engineer jobs?

For Pharmaceutical Project Engineer jobs, the most frequently searched job titles are:

Pharmaceutical Project Engineer jobs near you
Infographic showing various Pharmaceutical Project Engineer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 86% Full Time, 8% Part Time, and 4% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $90,644 per year, or $43.6 per hour.

Pharmaceutical Project Executive

Indianapolis, IN • On-site

Johnson Controls
Machinery Manufacturing • 10K+ employees
Learn more about Johnson Controlsexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago

Johnson Controls rating

8.0

Company rating: 8.0 out of 10

Based on 416 frontline employees who took The Breakroom Quiz

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 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: $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.

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About Johnson Controls

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Johnson Controls is a world leader in smart buildings, creating safe, healthy and sustainable spaces. For nearly 140 years, we’ve made buildings better and now we’re transforming them again with our award-winning digital technologies and services. We’re using artificial intelligence and data driven solutions to give you deeper insight into your building’s health, sustainability and performance. It’s changing the way we design, operate and maintain indoor environments and driving to a new era of autonomous buildings. We deliver the blueprint of the future for industries such as healthcare, schools, data centers, airports, stadiums, hotels, manufacturing and beyond through OpenBlue, our comprehensive suite of connected solutions. Johnson Controls offers the world’s largest portfolio of building technology, software and services. Supported by a team of more than 100,000 dedicated employees working across 150 countries, we’re helping customers achieve their sustainability goals and power their mission.

Industry

Machinery manufacturing, water transportation, public safety statistics centers and offices and manufacturing

Company size

10,000+ Employees

Headquarters location

Milwaukee, WI, US

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