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Client Project Manager II

Kindeva Drug Delivery
Posted 2 months ago, valid for 16 days
Location

Lexington, Fayette 40546, KY

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Kindeva, located in Lexington, KY, is seeking a Client Portfolio & Relationship Manager II with a minimum of 2 years of cGMP experience in the biotech or pharmaceutical industry.
  • The role involves enhancing client engagement, managing product lifecycles, and supporting operational planning while ensuring effective communication with both internal and external stakeholders.
  • Candidates should possess a B.S/B.A. degree in Project Management, Business, or a related field, with PMP certification preferred, along with strong interpersonal and communication skills.
  • This position offers significant growth potential within a rapidly expanding organization that manufactures life-saving nasal spray medications.
  • Salary details are not provided, but the role emphasizes the importance of continuous professional development and the opportunity to contribute to meaningful healthcare solutions.

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 Contract Development and Manufacturing Organization (CDMO) where your expertise will directly enhance client engagement, product lifecycle management, and operational excellence. As a Client Portfolio & Relationship Manager II, you will serve as a point of contact for assigned projects. Clients may include external CDMO customers or internal Kindeva product customers. This role works collaboratively with internal site resources and executes projects in accordance with the Kindeva client engagement and governance model.

The role supports effective and routine open communications and relationship management discussions with internal Kindeva functional groups, as well as external client groups. The Client Portfolio Relationship Manager II also supports operational planning at the site and works as part of the CPRM team to execute continual process improvement methods for enhancing client satisfaction and business growth.

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 & Communication

  • Supports client engagement model, which includes client management governance, and agreements on routine operational communications / meetings
  • Supports client communications associated with routine engagement, messaging, escalation, and notifications
  • Promptly notifies line management and executes required escalation process to support client issues

 

Operational & Project Support 

 

  • Responsible for supporting the product transfer to manufacturing
  • Responsible for interfacing with the Client and Kindeva to ensure all relevant product and process information is received
  • Supports creation of a project tracker, schedule, process flow, and Gantt chart for kickoff meetings
  • Tracks project change control and coordinates completion with the assigned owning department and owner
  • Supports obtaining all information for Manufacturing Science & Technology (MST) to complete new product forms and support manufacturing

 

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 promote understanding and achieve Client Portfolio & Relationship Management strategic objectives
  • Executes goals and accountabilities based on agreed objectives and results
  • Shares best practices across the CPRM team

 

Professional Development

  • Pursue continuous development, training, and workload management to strengthen professional and leadership capabilities

 

Qualifications:

Minimum Qualifications Required

  • B.S / B.A. degree in Project Management, Business or a related pharmaceutical sciences field or equivalent experience in regulated industry. PMP certification preferred.
  • 2+ years cGMP experience in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment, ideally pre-clinical phases through commercial, and / or equivalent amount of experience managing commercial operations or client portfolio management roles.
  • Familiarization of business and operational planning, forecasting, and impact of demand planning on biotech, pharmaceutical or bio-pharmaceutical manufacturing operations.
  • Interpersonal and collaborative / facilitative skills across functions, across internal business enterprise, and externally with multiple clients within a portfolio.
  • Strong communication skills, oral and written across stakeholders.
  • Ability to work in a team setting with minimal supervision.
  • Proficiency in MS Office, Teams, and project management software (e.g., MS Project, Smartsheet).
  • Delivery-focused mindset supporting personal accountability.

 

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

 

California residents should review our Notice for California Employees and Applicants before applying. 
 
 

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

 

 

Equal Opportunity Employer:
 

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today! 




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