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Project Manager Cdmo Jobs in Kentucky (NOW HIRING)

kindeva

Senior Client Project Manager

Lexington, KY · On-site

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 ...

kindeva

Senior Client Project Manager

Lexington, KY · On-site

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 ...

kindeva

Senior Client Project Manager

Lexington, KY · On-site

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 ...

kindeva

Senior Project Manager

Lexington, KY · On-site

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

kindeva

Senior Project Manager

Lexington, KY

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

kindeva

Senior Project Manager

Lexington, KY · On-site

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

kindeva

Senior Project Manager

Lexington, KY · On-site

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

kindeva

Senior Project Manager

Lexington, KY · On-site

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

Piramal Pharma Limited

Project Manager I

Lexington, KY

... CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We ... Project Management Location: Lexington Job Overview Reporting to the Director of Project Management ...

kindeva

Senior CPR Project Manager II

Lexington, KY · On-site

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client ... As a Senior Client Portfolio & Relationship Manager (Sr. CPRM) , you will serve as the primary ...

kindeva

Senior CPR Project Manager II

Lexington, KY

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client ... As a Senior Client Portfolio & Relationship Manager (Sr. CPRM) , you will serve as the primary ...

kindeva

Senior CPR Project Manager II

Lexington, KY

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client ... As a Senior Client Portfolio & Relationship Manager (Sr. CPRM) , you will serve as the primary ...

kindeva

Senior CPR Project Manager II

Lexington, KY · On-site

Join a rapidly expanding pharmaceutical CDMO where your expertise will directly enhance client ... As a Senior Client Portfolio & Relationship Manager (Sr. CPRM) , you will serve as the primary ...

Piramal Pharma Limited

Project Manager I

Lexington, KY · On-site

... CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We ... Project Management Location: Lexington Job Overview Reporting to the Director of Project Management ...

Bionova Scientific, Inc.

$260 - $295/hr

... CDMO sector.The position combines hands-on program leadership -- client relationships, project plans, risk management, and team development -- with the coordination, tracking, and executive ...

BrainChild Bio, Inc.

$150 - $180/hr

Responsibilities Supply Planning & CDMO Oversight * Lead demand forecasting and supply planning ... Strong analytical, project management, and problem-solving skills. * Experience working within GxP ...

Celmark International

$150 - $200/hr

Strong leadership, project management, and organizational skills. * Strong customer-facing ... Contract manufacturing/CMO/CDMO experience strongly required. Success Factors * Product development ...

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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 Kentucky?

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

What job categories do people searching Project Manager Cdmo jobs in Kentucky look for?

The top searched job categories for Project Manager Cdmo jobs in Kentucky are:

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

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

Project Manager Cdmo jobs near you

Senior Client Project Manager

Kindeva Drug Delivery Company

Lexington, KY • On-site

$90 - $110/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

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

Why Kindeva?

  • Collaborative team culture
  • Direct impact on patient care

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.

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.

Job Family B - Project Management Office - Client Portfolio Relationship Ma

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