Senior Client Project Manager

Kindeva Drug Delivery Company; Lexington (KY); On-site; USD 90,000 - 110,000; Full time

Benefits offered by this job

Professional development opportunities

Collaborative team culture

Job summary

Kindeva Drug Delivery Company in Lexington, KY, is seeking a Senior Client Project Manager (Sr. CPM) to enhance client engagement and manage product lifecycles within a rapidly expanding pharmaceutical environment.

The role involves overseeing client communications, collaborating across functions, and ensuring project success. Candidates must have a BS in engineering or a related field, a strong background in GMP practices, and 5+ years of industry experience.

Join us in our mission to manufacture life-saving medications and make a positive impact on patient health.

Qualifications

• 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.

Responsibilities

• Execute and manage the client engagement model.
• Collaborate across Quality, Manufacturing, and Technical Operations.
• Organize and oversee product transfers to manufacturing.
• Support operational and business planning.

Skills

GMP pharmaceutical manufacturing

Technical transfers

cGMP knowledge

GAMP5 understanding

Strong communication skills

Education

BS in engineering or related degree

Master's degree (preferred)

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