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Manager Cdmo Jobs in Virginia (NOW HIRING)

... CDMO, distribution, healthcare providers, payors, and healthtech. Recruiting for this role ends on ... As a Manager, Strategy, Growth, and Transformation on the M&A team, you will be a key member ...

... CDMO) dedicated to advancing patient outcomes through innovation, engineering excellence, and ... Lead automation projects to successful completion by managing technical scope, schedules, budgets ...

... CDMO) dedicated to advancing patient outcomes through innovation, engineering excellence, and ... Lead automation projects to successful completion by managing technical scope, schedules, budgets ...

Manager Cdmo information

What are Manager CDMO roles and responsibilities?

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 Virginia? The most popular types of Cdmo jobs in Virginia are:
What are popular job titles related to Manager Cdmo jobs in Virginia? For Manager Cdmo jobs in Virginia, the most frequently searched job titles are:
What cities in Virginia are hiring for Manager Cdmo jobs? Cities in Virginia with the most Manager Cdmo job openings:
Infographic showing various Manager Cdmo job openings in Virginia as of June 2026, with employment types broken down into 59% Full Time, and 41% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.
Process Lead - Global Supply Chain Excellence

Process Lead - Global Supply Chain Excellence

Catalent Pharma Solutions

Manassas, VA

$143K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

60th of 86 rated pharmaceutical


Job description

Process Lead - Global Supply Chain Excellence

Position Summary:

  • Full time salaried position

  • When not traveling, position required to be onsite at a US Catalent site

The Process Lead - Global Supply Chain Excellence is responsible for driving operational excellence, standardization, and continuous improvement across the end-to-end supply chain within Catalent's network. This role strengthens supply chain performance in a highly regulated, client-focused environment by optimizing planning, procurement, inventory management, logistics, and technology-enabled processes.
As a Process Lead - Global Supply Chain Excellence, this role partners closely with site Supply Chains, Finance, and IT to ensure reliable operations that meet client expectations, comply with GMP requirements, enable technology and support on-time delivery of clinical and commercial products.
Our Bridgewater location is the corporate office for Catalent.

The Role:

  • Support global supply chain processes excellence across planning, scheduling, materials management and warehouse logistics, aligning to GMP standards and CDMO business models

  • Establish harmonized process controls and KPIs to ensure consistency across sites

  • Host global forums (Best Practice sharing, SMEs, and cross-functional working groups) to drive alignment and structured governance

  • Lead Lean/Six Sigma-based improvement programs aimed at reducing cycle times, optimizing inventory, and supporting right-first-time performance

  • Drive optimization of current systems (ERP, MES) to support GMP-compliant and data-driven decision making

  • Lead implementation of advanced planning capabilities (capacity modeling, MPS/MRP improvements, Finite Scheduling, E2E analytics)

  • Identify and deploy digital tools that improve process robustness (workflow automation, dashboards, exception management tools)

  • Needs to be flexible for a work schedule which will need a combination of "work from home", travel and on-site presence

  • 25% annual global travel expectations

  • Other duties as assigned

The Candidate:

  • Bachelor's degree in Supply Chain, Operations, Engineering, Life Sciences, or related field, required

  • APICS or CPIM certification, desired

  • Minimum ten years of supply chain experience, ideally in pharmaceutical or CDMO environments

  • Experienced and adaptable to work fluidly across many cultures to build teams and improve customer results

  • Demonstrated experience in global process ownership or multi-site operations leadership

  • Strong understanding of GMP, regulatory expectations (FDA, EMA), and pharmaceutical quality systems

  • Expertise in Lean, Six Sigma, or similar continuous improvement methodologies

  • Proficiency with ERP (SAP, JDE/Oracle), MES and analytics platforms (Power BI)

  • Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds


Pay:

New Jersey Posting
The anticipated salary range for this position in New Jersey is $85,000 - $122,000, plus bonus, when eligible.The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent:

  • Defined career path and annual performance review and feedback process

  • 152 hours of PTO + 8 paid holidays

  • Several Employee Resource Groups focusing on D&I

  • Generous 401K match

  • Medical, dental and vision benefits effective day one of employment

  • Tuition Reimbursement

  • WellHub - program to promote overall physical wellness

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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