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Senior Continuous Improvement Specialist II

Kindeva


Job Location:

Lexington, KY - USA

Monthly Salary: Not provided by the employer
Posted: 30 July 2026 (30+ days ago)
Application Deadline: 27 October 2026
Vacancies: 1 Vacancy

Job Summary

Our Work MattersAt Kindeva we make products that save lives ensuring better health and well-being for patients around the KindevaPurpose-driven work environmentSignificant growth potentialCollaborative team cultureDirect impact on patient careIndustry-leading innovationAt Kindeva we manufacture products that improve the lives of patients around the world. Join a team where your expertise will directly support operational excellence in a highly regulated pharmaceutical manufacturing Impact You Will MakeAs the Senior Specialist Operational Excellence & Data Analytics you will play a critical role in driving operational excellence and continuous improvement across our manufacturing organization. Youll serve as a key liaison between Manufacturing Quality Assurance Supply Chain and Materials Management to ensure production teams have the resources documentation and data needed to operate efficiently while maintaining role combines operational excellence manufacturing support and data analytics to improve process performance streamline workflows and enhance manufacturing execution. Youll partner with cross-functional teams to implement Lean methodologies optimize production processes support manufacturing documentation and leverage data to drive informed decision-making throughout the Improvement & Operational ExcellenceLead and support continuous improvement projects aimed at optimizing manufacturing processes enhancing quality and reducing and implement process improvements related to resource coordination documentation flow process performance and inventory Kaizen events workshops and training sessions to promote a culture of continuous with cross-functional teams to implement Lean manufacturing tools and techniques such as 5S Six Sigma and lean inventory management with Manufacturing Supervisors to manage and analyze production data and equipment Documentation & PaperworkEnsure availability and distribution of production documentation including batch records logbooks and other manufacturing real-time review of production documentation for compliance and with Quality Assurance and Document Control to manage document life cycles and ensure current document versions are available for manufacturing documentation including Standard Operating Procedures (SOPs) Batch Records (BRs) and -Functional CollaborationPartner with Supply Chain and Materials Management teams to coordinate timely delivery of materials and proactively resolve inventory changes in production needs or material availability to prevent production detailed manufacturing schedules with input from Process Performance Maintenance Validation Engineering and other functional other responsibilities as school diploma or equivalent with 10 years of pharmaceutical manufacturing in using Lean tools and software applications such as Smartsheet Power BI Power Apps and similar of Good Manufacturing Practices (GMP) and regulatory requirements within the pharmaceutical to make sound decisions regarding compliance-related issues with moderate to manage multiple priorities and tasks in a dynamic written and verbal communication skills along with excellent organizational to work effectively within a team environment to maximize efficiency and RequirementsRegular use of hands to handle materials and to use electronic devices for extended periods throughout the to communicate effectively by telephone and electronic to regularly stand and walk for extended to occasionally lift and/or move up to 25 Impact of the RoleThis position will help strengthen manufacturing operations by driving continuous improvement initiatives enhancing operational performance through data-driven decision-making and ensuring manufacturing teams have the documentation materials and processes necessary to safely and efficiently produce life-changing pharmaceutical products. Success in this role will improve operational efficiency strengthen cross-functional collaboration and support Kindevas commitment to quality compliance and operational our One Team mission of manufacturing more tomorrows. Your expertise will help ensure better health and well-being for patients worldwide.#LI-Onsite #WH

Required Experience:

Senior IC


About Company

Kindeva: A purpose-fueled, people-centric, drug delivery CDMO dedicated to advancing your project, your ambitions and our industry.

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