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Pharmaceutical Project Manager Jobs (NOW HIRING)

Visium Resources, Inc.

Project Manager

Boulder, CO · On-site

The ideal candidate will possess strong pharmaceutical project leadership experience within biotech ... This role requires the ability to manage project schedules, budgets, risks, resources, and ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

$80K - $105K/yr

Pharmaceutical Manufacturing Position Type: Contract General The Project Manager will be responsible for leading and coordinating Capital Projects, Automation, Utilities, Infrastructure, and ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Coordinate project activities related to pharmaceutical Commissioning, Qualification, and ... Support document management activities, including organization, tracking, and version control ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Coordinate project activities related to pharmaceutical Commissioning, Qualification, and ... Support document management activities, including organization, tracking, and version control ...

MMR Consulting

PR · On-site

Salary: Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning ... Its services include Engineering, Project Management, and Validation. MMRConsulting ...

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Pharmaceutical Project Manager information

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$45K

$105K

$169.5K

How much do pharmaceutical project manager jobs pay per year?

As of Jun 20, 2026, the average yearly pay for pharmaceutical project manager in the United States is $105,026.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $128,500.00 per year, depending on experience, location, and employer.

Can I make 100k as a project manager?

A pharmaceutical project manager can earn a salary of $100,000 or more, depending on experience, education, location, and the complexity of projects managed. Senior project managers with certifications like PMP and strong leadership skills are more likely to reach or exceed this salary level.

What is a Pharmaceutical Project Manager job?

A Pharmaceutical Project Manager oversees drug development projects from initiation to completion, ensuring they meet regulatory, budget, and timeline requirements. They coordinate cross-functional teams, including researchers, regulatory specialists, and manufacturing professionals, to bring pharmaceutical products to market. Their responsibilities include risk management, resource allocation, and stakeholder communication. Strong project management skills, industry knowledge, and attention to compliance are essential for success in this role.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $140,000 annually, with median salaries around $115,000. Compensation varies based on experience, location, and company size, and often includes benefits such as bonuses and health insurance.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior executive roles such as Chief Scientific Officer, Vice President of Research and Development, or Chief Medical Officer tend to be the highest paying positions. These roles require extensive experience, advanced degrees, and leadership skills, often offering compensation packages that include high salaries, bonuses, and stock options.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Project Manager position, and why are they important?

A Pharmaceutical Project Manager needs a strong background in life sciences or pharmaceuticals, experience in project management, and often a relevant degree or certification such as PMP. Familiarity with tools like Microsoft Project, regulatory compliance systems (e.g., FDA or EMA guidelines), and document management platforms is crucial. Excellent communication, leadership, problem-solving, and organizational abilities set standout candidates apart. These skills are vital to effectively lead cross-functional teams, ensure regulatory compliance, and successfully deliver projects on time and within budget in a complex industry.

What does a project manager do in the pharmaceutical industry?

A pharmaceutical project manager oversees the planning, execution, and completion of drug development and manufacturing projects. They coordinate teams, manage budgets, ensure compliance with regulatory standards, and track project timelines using tools like Gantt charts and project management software. Strong organizational, communication, and regulatory knowledge are essential for success in this role.

What are the main challenges a Pharmaceutical Project Manager faces during a drug development project?

Pharmaceutical Project Managers often encounter challenges such as navigating complex regulatory requirements, managing tight project timelines, and coordinating across multiple departments like clinical research, regulatory affairs, and manufacturing. Ensuring effective communication among diverse stakeholders and addressing unforeseen obstacles, such as changes in trial protocols or supply chain disruptions, are also common. Strong organizational and leadership skills are essential for adapting to evolving project demands and keeping teams aligned. By anticipating challenges and fostering collaboration, Pharmaceutical Project Managers help ensure successful project outcomes and regulatory approvals.

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Pharmaceutical Project Manager jobs near you
Pharmaceutical Project Executive

Pharmaceutical Project Executive

Johnson Controls

Richmond, VA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 22 days ago

Johnson Controls rating

8.0

Company rating: 8.0 out of 10

Based on 386 frontline employees who took The Breakroom Quiz

133rd of 518 rated manufacturers

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: $150,000 - 185,000. USD 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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