Kindeva Drug Delivery · 5 days ago
Senior CPR Project Manager II
Lexington, KY
Full-time
Onsite
Senior Level
5+ years expKindeva Drug Delivery is a purpose-driven company focused on manufacturing life-saving nasal spray medications. The Senior CPR Project Manager II will serve as the primary point of contact for CDMO clients, driving client satisfaction and operational alignment throughout the product lifecycle.
Manufacturing
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
Qualification
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
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
Company
Kindeva Drug Delivery
Kindeva Drug Delivery is a global contract development and manufacturing organization (CDMO) in the pharmaceutical industry.
1001-5000 employees
H1B Sponsorship
Kindeva Drug Delivery has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2024 (4)
2023 (1)
2022 (3)
Funding
Current Stage
Late StageTotal Funding
$46.96MKey Investors
Global Britain Investment Fund
2023-08-03Grant· $41.96M
2022-11-14Acquired
2022-06-13Series Unknown· $5M
Leadership Team
Brian Schubmehl
Chief Human Resources Officer
Recent News
MarketScreener
2026-01-01
Company data provided by crunchbase