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Pharmaceutical Project Manager Jobs (NOW HIRING)

Lead pharmaceutical project planning, including objectives, scope, timelines, budgets, resources, and risk management. * Manage and motivate remote cross-functional teams in a collaborative ...

PR · On-site

Pharmaceutical Manufacturing Position Type: Contract Position Overview We are seeking an experienced and results-driven Project Portfolio Manager to lead and oversee a portfolio of capital and ...

PR · On-site

Pharmaceutical Manufacturing Position Type: Contract Position Overview We are seeking an experienced and results-driven Project Portfolio Manager to lead and oversee a portfolio of capital and ...

... pharmaceutical company, with pharmaceutical project management experience. 6. Experience in digitalization and automation. 7. Project management Professional (PMP) certification. 8. Experience ...

Bachelor's degree with 3+ years of pharmaceutical project management experience OR Associate degree with 4+ years of pharmaceutical project management experience OR High school diploma/GED with 6+ ...

PR · On-site

Pharmaceutical Manufacturing - Solid Dosage Position Type: Contract Position Overview We are seeking an experienced and results-driven Project Manager to lead and support capital and operational ...

PR · On-site

Pharmaceutical Manufacturing - Solid Dosage Position Type: Contract Position Overview We are seeking an experienced and results-driven Project Manager to lead and support capital and operational ...

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We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.

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Be Seen First

We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives.

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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 May 29, 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.

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.

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 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.
What cities are hiring for Pharmaceutical Project Manager jobs? Cities with the most Pharmaceutical Project Manager job openings:
What states have the most Pharmaceutical Project Manager jobs? States with the most job openings for Pharmaceutical Project Manager jobs include:
Infographic showing various Pharmaceutical Project Manager job openings in the United States as of May 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 95% Physical, and 5% Hybrid job distribution, with an average salary of $105,026 per year, or $50.5 per hour.
Pharmaceutical Project Manager

Pharmaceutical Project Manager

Catalent Pharma Solutions

Saint Petersburg, FL • On-site

Full-time

Life, PTO

Posted 13 days ago


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 70 rated pharmaceutical


Job description

Pharmaceutical Project Manager

The Pharmaceutical Project Manager will serve as the primary customer-facing leader responsible for managing end-to-end CDMO client projects across the full product lifecycle, from pre-clinical development through Phases I-IV and lifecycle management.

Position Summary

This position is on-site at the St. Petersburg site.

Join Catalent's flagship Softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility.

The Project Manager is responsible for ensuring customer satisfaction, timely clinical delivery, adherence to revenue forecast and budget, and effective cross-functional execution, all while maintaining compliance with cGMP, regulatory, quality, and safety standards required in a global, FDA-regulated CDMO setting.

The Role

  • Serve as the single point of contact for assigned CDMO clients.

  • Manage client relationships, including hosting site visits, governance meetings, and routine project updates.

  • Proactively monitor and manage customer satisfaction ("customer temperature"), addressing risks and escalations as needed.

  • Provide clear, timely, and professional communication to customers throughout the project lifecycle.

  • Ensure timely follow-up on decisions, risks, and deliverables.

  • Escalate critical path issues impacting schedule, cost, quality, or compliance.

  • Coordinate and conduct phase gate review and approval prior clinical manufacturing for each development phase and/or prior registration, validation, and major regulatory changes.

  • All other duties as assigned.

The Candidate

  • Bachelor's degree is required; preferably in a scientific field, including, but not limited to, Chemistry, Biology, Pharmacy, Chemical and Mechanical engineering with at least 5 years of industry experience is required; preferably in the pharmaceutical industry, and most preferably with an FDA-regulated CDMO company.

  • Working knowledge of project management principles and concepts in a cGMP environment is required.

  • At least 2 years of project management experience or other experience that demonstrates successful team leadership and project management acumen.

  • PMP certification is preferred.

  • PC skills, including training on Microsoft Project, Outlook, Excel, Word, PowerPoint, WorkFront and other Catalent software packages are required.

  • Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 40.09 pounds without assistance.

  • Be accessible to manufacturing floor and office staff and to use required office equipment.

  • Specific vision requirements include reading of written documents and frequent use of computer monitor.

Why You Should Work At Catalent

  • Spearhead exciting and innovative projects

  • Fast-paced, dynamic environment

  • High visibility to members at all levels of the organization

  • 152 hours of PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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