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Manager Cdmo Jobs in Florida (NOW HIRING)

Evergen

Facilities Engineer 2

Alachua, FL · On-site

$80K - $95K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Experience * 4-6 years of experience in project management, critical engineering systems, or ...

Evergen

Buyer 2

Alachua, FL · On-site

$65K - $80K/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

Evergen

Purchasing Manager

Alachua, FL · On-site

$110K - $120K/yr

Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in ... Lead and manage team performance through goal setting, coaching, and feedback; ensure consistent ...

Evergen

Operations Supervisor

Alachua, FL · On-site

$65K - $80K/yr

... CDMO) in regenerative medicine. As the only regenerative medicine company that offers a ... Interfaces with Operations Management Team regarding production needs and challenges as well as ...

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 ...

Ourvita

Account Manager - Remote

Largo, FL

Ourvita is the largest Europe-based CDMO for food supplements, with a strong global presence ... The Account Manager will serve as the liaison to grow our business. It is the Account Manager ...

Jacobs Management Group

Packaging Engineer

Alachua, FL

$65K - $80K/yr

Work for a global CDMO with manufacturing facilities across the US, Europe, and New Zealand...real scale, real impact * Own packaging engineering end-to-end: design, prototyping, validation, and ...

Celmark International

R&D Formulator

Orlando, FL · On-site

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

System One

Sr QC Chemist

Boca Raton, FL · On-site

$90K - $110K/yr

Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an experienced Quality ... Perform sampling and testing for raw and packing materials, managing distribution of work among 2-3 ...

System One

Sr QC Chemist

Boca Raton, FL · On-site

$90K - $110K/yr

Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an experienced Quality ... Perform sampling and testing for raw and packing materials, managing distribution of work among 2-3 ...

System One

Sr QC Chemist

Boca Raton, FL · On-site

Work Model: Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an ... Perform sampling and testing for raw and packing materials, managing distribution of work among 2-3 ...

System One Holdings, LLC

Sr QC Chemist

Boca Raton, FL · On-site

$90K - $110K/yr

Onsite - onsite Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an experienced Quality ... managing distribution of work among 2-3 team members from sample collection to result generation ...

Quotient Sciences

Screening Deputy Lead

Miami, FL · On-site

$111K/yr

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... The Role: * Assist the Screening Manager in tracking performance of screening activities for ...

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Manager Cdmo information

What are the roles and responsibilities of a Manager CDMO?

A Manager CDMO (Contract Development and Manufacturing Organization) oversees the relationship and project management between a pharmaceutical or biotech company and external CDMO partners. Their responsibilities include coordinating project timelines, ensuring regulatory compliance, managing budgets, and facilitating communication between internal teams and the CDMO. They play a key role in ensuring that drug development and manufacturing projects meet quality standards and are delivered on time. The Manager CDMO also addresses any issues that arise during the project lifecycle and ensures alignment with company objectives.

What are the key skills and qualifications needed to thrive as a Manager CDMO, and why are they important?

To thrive as a Manager CDMO (Contract Development and Manufacturing Organization), you need a solid background in pharmaceutical or biotechnology processes, project management expertise, and a relevant science or engineering degree. Familiarity with quality management systems (QMS), regulatory compliance tools (like GMP, ISO), and project tracking software is typically required. Strong leadership, negotiation, and interpersonal communication skills help in managing cross-functional teams and client relationships. These skills and qualifications are vital for ensuring project success, regulatory adherence, and client satisfaction in a highly regulated and competitive industry.

How does a Manager CDMO typically interact with clients and internal teams to ensure project success?

A Manager CDMO (Contract Development and Manufacturing Organization) acts as a key liaison between clients and various internal departments such as R&D, quality assurance, and manufacturing. They coordinate project timelines, communicate client requirements, and address any issues that arise to keep projects on track. Effective collaboration and clear communication are essential, as managers often facilitate meetings, provide regular updates, and align cross-functional teams to meet client expectations and regulatory standards. This role requires strong organizational skills and the ability to adapt to shifting client needs.

What is the difference between Manager Cdmo vs Project Manager?

AspectManager CdmoProject Manager
CredentialsTypically requires life sciences or pharmaceutical management experience, relevant certifications (e.g., PMP, regulatory training)Requires project management certifications (e.g., PMP), often with industry-specific experience
Work EnvironmentWorks within pharmaceutical or biotech companies, overseeing clinical development or manufacturingWorks across industries, managing projects in various sectors including healthcare, IT, construction
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and contract manufacturing organizationsUsed across multiple industries, including healthcare, construction, IT, and engineering

The Manager Cdmo primarily focuses on managing contract development and manufacturing operations within the pharmaceutical industry, requiring specialized industry knowledge. In contrast, a Project Manager oversees various projects across industries, emphasizing project execution and delivery. While both roles involve leadership and coordination, the Manager Cdmo's expertise is more industry-specific, especially in regulated environments.

What are the most commonly searched types of Cdmo jobs in Florida? The most popular types of Cdmo jobs in Florida are:
What are popular job titles related to Manager Cdmo jobs in Florida? For Manager Cdmo jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Manager Cdmo jobs in Florida look for? The top searched job categories for Manager Cdmo jobs in Florida are:
What cities in Florida are hiring for Manager Cdmo jobs? Cities in Florida with the most Manager Cdmo job openings:
Manager Cdmo jobs near you

Facilities Engineer 2

Evergen

Alachua, FL • On-site

$80K - $95K/yr

Full-time

Re-posted 26 days ago

Job description

Location: Alachua, FL

Annual CIP bonus opportunity of up to $8,000


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, DE., Glasgow, UK., and Marton, NZ.


Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://lnkd.in/eMSfVJkM

RESPONSIBILITIES

  • Provides engineering support for maintenance of a biotech manufacturing plant with a focus on critical engineering systems (CES)
  • Applies engineering principles to research, design, identify, install, document, validate, and make improvements to equipment and systems
  • Provides engineering support, troubleshoots, problem-solves, and resolves issues with equipment and systems
  • Prepares design drawings, plans, and specifications for engineering projects
  • Supports the engineering design process for assigned projects, with responsibility for successful adherence to company standards, specifications, budgets, schedules, and regulatory requirements
  • Evaluates the feasibility and cost of implementing proposed engineering projects and performs economic analyses on major equipment items
  • May occasionally work alternative hours or weekends during critical equipment maintenance
  • Analyzes workflow, space requirements, and equipment layout in order to maximize efficiency
  • Proactively collaborates with other functions to identify possible solutions to improving productivity, efficiency, simplification, or support innovation while ensuring projects are completed on-time
  • Identifies risks in processes or assets using analytical tools and works with stakeholders in mitigating risks
  • Prepares project plans and reports to proactively share with stakeholders
  • Other duties as assigned

REQUIREMENTS:

Education

  • Bachelor’s degree in engineering discipline or a relevant field preferred.


Experience

  • 4-6 years of experience in project management, critical engineering systems, or related field
  • Experience may substitute for education requirement

Certification

  • N/A

Skills

  • Microsoft Office Suite, advanced Excel
  • Lean Manufacturing Processes
  • Statistical Methods and Analysis
  • Current Good Manufacturing Processes
  • Computer Aided Drafting software
  • Project Management software
  • Excellent verbal and written communication
  • Technical Writing

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 Evergen in 2020 and has supported the transformation of the company to its next level of potential.


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