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Project Manager Cdmo Jobs in Florida (NOW HIRING)

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 ...

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... Prepares study binders for source document storage as instructed by Project Management * Supports ...

... CDMO/CMO environment · Strong understanding of ingredient functionality, solubility, stability ... ability to manage multiple projects simultaneously · Working knowledge of FDA and cGMP ...

Material Handler

Miami, FL · On-site

$18/hr

... CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical ... Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a ...

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Project Management * Continuous Improvement * MS Office * Proficiency in computer-aided design (CAD ...

File Clerk - Per Diem

Miami, FL · On-site

$15.75 - $19/hr

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... To support the Project Management team in filing and archiving of study documents * To assist with ...

File Clerk - Per Diem

Miami, FL · On-site

$15.75 - $19/hr

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... To support the Project Management team in filing and archiving of study documents * To assist with ...

Accountable to work with key account managers and customer supply chain leaders / master planners ... Capture accurately the demand emerging from CDMO+ business. * Identify demand plan gaps against ...

Office Coordinator

Gainesville, FL · On-site

$16.25 - $21.75/hr

... CDMO) with the mission to streamline CMC development, apply expertise in analytical and process ... Manage candidate communications and interview scheduling. * Update and maintain job postings for ...

Showing results 21-37

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.

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 are the key skills and qualifications needed to thrive as a project manager in a CDMO, 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.

What are popular job titles related to Project Manager Cdmo jobs in Florida?

For Project Manager Cdmo jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Project Manager Cdmo jobs?

Cities in Florida with the most Project Manager Cdmo job openings:

Infographic showing various Project Manager Cdmo job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Sr. Quality Engineer

Evergen

Alachua, FL • On-site

$90K - $115K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 days ago


Job description

Location: Alachua, FL

Annual Bonus Opportunity up to $10,000.00

Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN; Eden Prairie and Glencoe, MN; Neunkirchen, Germany; Glasgow, UK; and Marton, New Zealand.

We are proud to be Great Place to Work® Certified in 2026, reflecting our commitment to creating an exceptional employee experience and workplace culture. Evergen currently has full-time career opportunities available across multiple locations.

Our comprehensive benefits package includes:

  • Paid Time Off (PTO)
  • 401(k) with up to a 6% company match
  • Holiday pay
  • Medical, dental, and vision insurance
  • Short-term and long-term disability coverage
  • Paid parental leave and much more!

Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://www.linkedin.com/company/evergenbio

RESPONSIBILITIES

  • Serves as a lead core team member of cross functional project teams whose responsibilities include coordinating deliverables for the improvement of processes across the manufacturing facility
  • Supervises the Quality Assurance Engineering team including performance management, corrective action, hiring and selection, and allocation of engineering support as it relates to quality assurance initiatives
  • Reviews quality Key Performance Indicator (KPI) data and actions to ensure continuous improvement in collaboration with various operations value streams
  • Reviews validations and risk management activities to support regulatory submissions, sustaining activities, and product launches are on time and have a high level of customer and patient focus
  • Leads and conducts problem solving through change management, nonconformance workflows, and continuous improvement or new product development initiatives
  • Reviews and edits nonconformance investigation and disposition phases for team members and assists in the preparation and presentation of materials for quality initiatives
  • Other duties as assigned

REQUIREMENTS

Education

  • Bachelor’s degree in relevant technical discipline

Experience

  • 6+ years of relevant medical device, pharmaceutical, or other regulated industry experience.
  • *Combination of advanced degree and experience may be considered.

Certification

  • AATB or CTBS Certification, preferred
  • Lead Auditor Certification, preferred
  • ASQ – CQE, CBA, or CQA, preferred

Skills

  • Excellent verbal and written communication
  • Technical writing
  • Problem solving methodologies
  • Microsoft Office Suite
  • Quality Management System software
  • Investigations
  • Statistical techniques

Travel

  • N/A

SAFETY

Physical Requirement

  • Move or lift objects up to 25 pounds
  • Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays
  • Frequent (>75%) fine manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.)

Working Environment

  • Onsite: Office environment with assigned workstation
  • Remote positions only: Home office environment with minimum distractions

More about Evergen:

Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management.


Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values:

  • Accountable: We own our actions and decisions.
  • Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth.
  • Growth Mindset: We embrace challenges as opportunities for continuous learning.
  • Customer-Centric: We prioritize customers at every touch point.
  • Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated.

At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success.

Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential.

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