Kindeva Drug Delivery

CPR Project Coordinator

Kindeva Drug Delivery  •  Bridgeton, MO (Onsite)  •  3 hours ago
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Job Description

Our Work Matters
At Kindeva, we make products that improve people's lives. Every day, our teams help develop and manufacture pharmaceutical therapies that patients around the world depend on. As a Client Project Coordinator, you'll play an important role in helping deliver customer projects on time by supporting our Client Project Management team and ensuring projects stay organized, on track, and well communicated.

Why Kindeva?
• Purpose-driven work environment
• Significant growth potential
• Collaborative team culture
• Direct impact on patient care
• Industry-leading innovation

The Impact You Will Make
Transform Lives Through Innovation As a Client Project Coordinator, you will provide administrative and operational support to the Client Project Management team for technology transfer and commercial manufacturing projects. You'll help maintain project documentation, coordinate meetings, track project milestones, and facilitate communication between internal cross-functional teams and external clients. Your organizational skills and attention to detail will help ensure projects move forward efficiently while supporting exceptional customer service.

Responsibilities
• Support Client Project Managers with day-to-day coordination of customer projects.
• Schedule and coordinate internal and client meetings.
• Prepare meeting agendas, capture meeting minutes, and distribute action items.
• Maintain project documentation and ensure project files remain current.
• Update project schedules, trackers, dashboards, and Gantt charts.
• Monitor project timelines and communicate status updates to the project team.
• Assist with preparation of governance presentations, business reviews, and customer communications.
• Coordinate information between Manufacturing, Quality, Supply Chain, Engineering, Technical Services, Finance, and other functional groups.
• Track project deliverables and follow up on outstanding action items.
• Escalate potential project delays or risks to the Client Project Manager.
• Support performance reporting and project metrics.
• Maintain a high level of professionalism while interacting with internal stakeholders and external clients.
• Perform other duties as assigned.

Qualifications

Required
• Bachelor's degree in business, Life Sciences, Engineering, or a related field, or equivalent experience.
• Minimum of two (2) years of project coordination, project administration, customer service, or operations support experience.
• Strong organizational and time management skills.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office, including Excel, PowerPoint, Outlook, and Teams.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong attention to detail and follow-through.

Preferred
• Experience supporting projects within the pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment.
• Experience working within a CDMO or GMP environment.
• Familiarity with project management tools such as Microsoft Project or Smartsheet.
• Experience coordinating cross-functional teams and customer-facing projects.

Physical Requirements
• Ability to work in an office environment.
• Occasional travel between sites or customer meetings may be required.
• Ability to sit, stand, and use a computer for extended periods.

#LI-Onsite #WH

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!
Kindeva Drug Delivery

About Kindeva Drug Delivery

Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.

For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.

Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.

Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.

Because every patient deserves tomorrow.

For more information about how we can transform tomorrows together, please visit www.kindevadd.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Woodbury, Minnesota
Year Founded
2020
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