Senior CPR Project Manager II

Kindeva; Lexington (KY); On-site; USD 120,000 - 170,000; Full time

Job summary

Kindeva in Lexington, KY is seeking a Senior Client Portfolio & Relationship Manager to be the primary contact for a portfolio of CDMO clients. You will drive client satisfaction, oversee governance, and coordinate with Quality and Technical Process Engineering teams to align on product lifecycle.

The role offers opportunity to influence client engagements, transfer processes, and continuous improvement initiatives, with growth potential as the Lexington facility expands.

Qualifications

• 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.

Responsibilities

• 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 timely delivery of product and process information
• 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
• 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
• 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
• Pursue continuous development, training, and workload management to strengthen professional and leadership capabilities

Skills

Communication skills

Client relationship management

Cross-functional collaboration

Education

BS in engineering/related degree or equivalent experience

Tools

Gantt charts

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 Portfolio & Relationship Manager (Sr. CPRM), 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 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