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Project Manager Cdmo Jobs in Florida (NOW HIRING)

Evergen

Sr. R&D Project Manager

Alachua, FL · On-site

$100K - $125K/yr

This rebranding reflects our strategic evolution as a leading CDMO in regenerative medicine and ... Has subject matter expertise across all knowledge areas of project management and uses this ...

Evergen

Operations Engineer 2

Alachua, FL · On-site

$80K - $90K/yr

Project management * Problem-solving methodologies * Technical writing * Statistical methods and ... our position as the CDMO of Choice in regenerative medicine solutions. We recognize that ...

Evergen

Operations Manager

Alachua, FL · On-site

$100K - $120K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Project Management * Process Improvement Methodologies Travel * N/A Safety: Physical Requirement

Evergen

Buyer 2

Alachua, FL · On-site

$65K - $75K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Manages project lead times and provides up-to-date information to project manager when needed

Ion Labs, Inc.

Account Manager - Remote

Largo, FL · On-site +1

Description Ourvita is the largest Europe-based CDMO for food supplements, with a strong global ... Using Project Management tools to onboard customers, sponsor projects and serve as key contact ...

New

Evergen

Operations Engineer 2

Alachua, FL · On-site

$75K - $95K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Executes project management leadership for multiple projects including leading core team meetings ...

Evergen

Sr. Quality Engineer

Alachua, FL · On-site

$90K - $115K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... RESPONSIBILITIES * Serves as a lead core team member of cross functional project teams whose ...

Deloitte

M&A Data Analytics Manager - LSHC

Tampa, FL · On-site

... CDMO, distribution, healthcare providers, payors, and healthtech. Work you'll do: As a Manager ... projects. A successful candidate would possess these skills: Ability to work independently and ...

Deloitte

M&A Data Analytics Manager - LSHC

Tampa, FL

Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... CDMO, distribution, healthcare providers, payors, and healthtech. Recruiting for this role ends on ...

Deloitte

M&A Data Analytics Manager - LSHC

Miami, FL

Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... CDMO, distribution, healthcare providers, payors, and healthtech. Recruiting for this role ends on ...

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Project Manager Cdmo information

What is a Project Manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.

What does a project manager at a pharmaceutical company do?

A project manager at a pharmaceutical company oversees the planning, execution, and completion of drug development and clinical trial projects. They coordinate teams, manage budgets, ensure regulatory compliance, and track project timelines using tools like Gantt charts and project management software. Their role ensures projects meet scientific, regulatory, and business objectives efficiently.

What are the key skills and qualifications needed to thrive as a Project Manager in a CDMO (Contract Development and Manufacturing Organization), and why are they important?

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

How does a Project Manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.

What is the highest paying project manager?

The highest paying project managers are often those working in industries like technology, finance, or pharmaceuticals, with senior roles such as Program Manager or Portfolio Manager earning top salaries. Certifications like PMP and experience managing large, complex projects can also contribute to higher compensation, especially in regions with high demand for project management expertise.

Can I make 100k as a project manager?

Project managers, especially in the pharmaceutical or biotech industries, can earn $100,000 or more annually depending on experience, location, and certifications like PMP. Senior project managers or those working in high-demand sectors often have higher earning potential, with salaries influenced by project complexity and company size.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior roles such as Vice President of Research and Development or Chief Scientific Officer tend to be the highest paying positions, often earning six-figure salaries. Project Managers in CDMO companies with extensive experience and advanced certifications can also earn high compensation, especially when overseeing large-scale projects or managing multiple teams.
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Infographic showing various Project Manager Cdmo job openings in Florida as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Pharmaceutical Project Manager

Pharmaceutical Project Manager

Catalent, Inc.

Saint Petersburg, FL • On-site

Full-time

Life, PTO

Re-posted 27 days ago

Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

50th of 74 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.

What Catalent employees say

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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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