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Senior CPR Project Manager II
Kindeva
- Lexington, Kentucky, United States
- Lexington, Kentucky, United States
Über
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.
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Sprachkenntnisse
- English
Hinweis für Nutzer
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