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Manager Cdmo Jobs in Florida (NOW HIRING)

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 ...

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

Quality Control Chemist

Boca Raton, FL ยท On-site

$70K - $90K/yr

Onsite, Monday - Friday Day Overview Developing 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 ...

Screening Deputy Lead

Miami, FL ยท 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 ...

Office Coordinator

Gainesville, FL ยท 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 ...

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 ...

With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and ... To support project management in the completion of allocated projects to the agreed standards of ...

Material Handler

Miami, FL ยท 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 ...

Showing results 41-60

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.

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 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.

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 cities in Florida are hiring for Manager Cdmo jobs?

Cities in Florida with the most Manager Cdmo job openings:

Sr QC Chemist

Boca Raton, FL โ€ข On-site

System One
Business Consulting Servicesย โ€ขย 5 - 10K employees

Other

Medical, Dental, Vision, Life, Retirement

Re-posted 3 days ago


Job description

Job Title: Sr QC Chemist Location: Boca Raton, FL Type: Direct Hire Compensation: Work Model: Onsite – onsite

Overview Pharmaceutical CDMO in Boca Raton, FL is seeking an experienced Quality Control Chemist to join their team on a direct hire basis!

Responsibilities • Review/test raw materials (RM), packaged materials (PM), in-process (IP), and finished products to ensure quality standards are met. • Conduct method transfer and verification, including investigation of out-of-specification (OOS) and out-of-trend (OOT) results. • Ensure laboratory compliance through audits and data integrity practices. • Perform sampling and testing for raw and packing materials, managing distribution of work among 2-3 team members from sample collection to result generation. • Prepare specifications for raw materials, packing materials, and finished products according to USP/US Pharmacopeia standards. • Perform chemical testing using techniques such as FTIR, Karl Fischer titrations, and UV-Vis spectroscopy. • Review and approve test limits and testing procedures based on pharmacopeial requirements.

Requirements • BS/MS in Chemistry, Pharmacy, Pharmaceutical Sciences, Microbiology, or related discipline. • 5-8 years of QC experience in pharmaceutical sterile injectable manufacturing. • Experience with USP/US Pharmacopeia, including preparation of specifications and chemical testing. • Proficiency in FTIR, Karl Fischer Titrations, and UV-Vis techniques. • Strong knowledge of method transfer, investigations (OOS/OOT), and laboratory compliance. • Ability to review data, perform audits, and maintain data integrity.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-3 #LI-GS1 Ref: #558-Scientific


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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US