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Manager Cdmo Jobs in Kentucky (NOW HIRING)

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Project Manager ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Project Manager ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Project Manager ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Portfolio ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Portfolio ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Project Manager ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Portfolio ...

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Portfolio ...

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

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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 popular job titles related to Manager Cdmo jobs in Kentucky? For Manager Cdmo jobs in Kentucky, the most frequently searched job titles are:
What cities in Kentucky are hiring for Manager Cdmo jobs? Cities in Kentucky with the most Manager Cdmo job openings:

Senior Client Project Manager

kindeva

Lexington, KY

Other

Re-posted 6 days ago


Kindeva rating

6.7

Company rating: 6.7 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

Why Kindeva?

  • Purpose-driven work environment
  • Significant growth potential
  • Collaborative team culture
  • Direct impact on patient care
  • Industry-leading innovation

At Kindeva – Lexington, KY, we're not just making products – we're manufacturing life-saving nasal spray medications that make a difference.

 

The Impact You Will Make:

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Senior Client Project Manager (Sr. CPM), you will serve as the primary point of contact for a portfolio of CDMO clients. Working cross-functionally with Quality and Technical Process Engineering teams, you will drive client satisfaction, business growth, and operational alignment throughout the product lifecycle.

Growth Opportunity

Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions.

 

Responsibilities:

Client Engagement & Governance

  • Execute and manage the client engagement model, including governance structure, operational communications, and business performance reviews
  • Manage routine client communication, escalation, and notifications to ensure transparency and alignment
  • Serve as the primary interface between clients and Kindeva, ensuring the timely delivery of product and process information

 

Operational Management

 

  • Collaborate across Quality, Manufacturing, and Technical Operations to support client and product needs
  • Organize and oversee product transfers to manufacturing
  • Develop and maintain project trackers, schedules, process flows, and Gantt charts for kickoff and ongoing client projects
  • Track and coordinate project change controls through completion

 

Business Planning & Process Improvement

  • Execute goals and accountabilities based on agreed-upon objectives and results
  • Support operational and business planning, including forecasting, budgeting, and performance tracking
  • Share best practices across functions and maintain standard operating procedures to ensure consistency and quality
  • Review and execute process improvement initiatives to enhance client satisfaction and business efficiency

 

Cross-Functional Collaboration

  • Collaborate with other functional areas to achieve Client Portfolio & Relationship Management strategic objectives
  • Notify line management and Quality leadership of potential issues or risks promptly
  • Coordinate with Manufacturing Science & Technology (MST) to complete product forms and support manufacturing activities

 

Professional Development

  • Pursue continuous development, training, and workload management to strengthen professional and leadership capabilities

 

Qualifications:

Minimum Qualifications Required

  • BS in engineering/related degree or equivalent experience
  • 5+ years of related experience with a Bachelor’s degree; or 3 years with a Master’s degree
  • Previous work experience in GMP pharmaceutical manufacturing and technical transfers
  • Working knowledge of cGMP, GAMP5, and regulatory requirements

Preferred Qualifications

  • Experience working with nasal spray products/devices or related drug-delivery technologies
  • Strong technical and nontechnical communication skills
  • Experience supporting client/regulatory audits and follow-up responses
  • Extensive technical writing experience

Join our One Team mission of manufacturing more tomorrows. Your expertise will help ensure better health and well-being for patients worldwide.

# LI-Onsite


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