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  • Germantown, MD, USA ● Req #1985
    Thursday, July 3, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Combination Product Development team is a dynamic, growing part of Kindeva’s Development Services organization. We have recently opened a facility in Germantown, MD and are seeking talented team members to help us provide customers in each major drug delivery combination product segment with a comprehensive offering of market-ready combin ... More
  • Lexington, KY, USA ● Req #1939
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Manufacturing Team Leader at our Lexington facility, you will play a vital role in leading daily production operations, ensuring adherence to Good Manufacturing Practices (GMP), and driving efficiency and quality across a designated production area. You will directly support and develop production technicians, oversee compliance and training, and help deliver l ... More
  • Lexington, KY, USA ● Req #1938
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Manufacturing Team Leader at our Lexington facility, you will play a vital role in leading daily production operations, ensuring adherence to Good Manufacturing Practices (GMP), and driving efficiency and quality across a designated production area. You will directly support and develop production technicians, oversee compliance and training, and help deliver l ... More
  • Lexington, KY, USA ● Req #2008
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: As a Validation Engineer, you will play a key role in supporting the qualification and validation activities that ensure our manufacturing processes and equipment meet rigorous regulatory and quality standards. Your expertise will help maintain compliance with cGMP and industry guidelines, contributing to the reliable production of safe a ... More
  • Lexington, KY, USA ● Req #1997
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: As a Senior Scientist in Product Development, you will be a scientific leader independently driving complex formulation and combination product development activities. You will support the design, development, and commercialization of drug-device combination products, significantly contributing to product strategy, regulatory submissions, ... More
  • Lexington, KY, USA ● Req #1996
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: As the Analytical Development Manager, you will lead and oversee analytical activities supporting drug substance and drug product development across all phases of the product lifecycle. You will ensure successful development, validation, and transfer of analytical methods with a focus on scientific excellence, regulatory compliance, and c ... More
  • Lexington, KY, USA ● Req #1998
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: As an Analytical Scientist II, you will be a key contributor to the development, validation, and transfer of analytical methods that ensure the quality and safety of our pharmaceutical products. Your expertise will directly support drug substance and product development, enabling reliable manufacturing processes and regulatory compliance. ... More
  • Lexington, KY, USA ● Req #1962
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: As a Senior Quality Assurance Specialist I, you will play a pivotal role in ensuring the highest standards of product quality and regulatory compliance. You will provide leadership and technical expertise to the QA team while driving quality improvement initiatives across the organization. Your contributions will directly support the deli ... More
  • St. Louis, MO, USA ● Req #1933
    Wednesday, July 2, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The aseptic manufacturing engineer is a key technical role responsible for ensuring consistent high performance of aseptic manufacturing processing areas. The role requires specialized aseptic manufacturing and compliance experience. The incumbent will provide focused technical ownership over manufacturing processes while driving quality, the ... More
  • 19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1865
    Tuesday, July 1, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.    The Impact You Will Make The Scheduler is a highly organized and detail-oriented individual who can develop and manage production schedules while aligning with APICS principles and best practices. This role requires strong analytical skills, cross-functional collaboration, and expertise in supply chain management.   Responsibilities   Develop and maintain MRP-bas ... More
  • St. Louis, MO, USA ● Req #1966
    Tuesday, July 1, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make This position will be responsible for performing investigational analysis and testing activities in the Quality Development Support Laboratory along with managing protocols and experimental studies. This includes performing visual and functional evaluations, measurements, and testing as well as coordinating and overseeing testing performed by ... More
  • 11200 Hudson Rd, Woodbury, MN 55129, USA ● Req #1911
    Monday, June 30, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make This is an excited opportunity as a Advanced Manufacturing Specialist to lead the manufacturing responsibilities for the NPI (New Product Introduction) teams to scale up products / processes that meet our manufacturing strategies and objectives. You will also be working with our contract manufacturing facilities globally and a diverse suppli ... More
  • Lexington, KY, USA ● Req #1960
    Monday, June 30, 2025
    Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make: If you are ready to work for a purpose, join Kindeva Drug Delivery! Working on the KDD Manufacturing Team as a Manufacturing Technician, you will play a crucial role in supporting the manufacturing of life-changing and life-saving prescription nasal spray medications. The Lexington location is experiencing exponential growth. Join our te ... More
  • Lexington, KY, USA ● Req #1979
    Monday, June 30, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. As a Senior Specialist, Operational Excellence, you will play a key role in driving performance and fostering a culture of continuous improvement across our Lexington manufacturing site. You will lead cross-functional initiatives that improve efficiency, reduce waste, and enhance quality using Lean, Six Sigma, and structured problem-solving methodologies. Your abili ... More
  • Lexington, KY, USA ● Req #1967
    Monday, June 30, 2025
    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 testing products – we’re ensuring the safety and quality of nasal spray medications that make a difference.   The Impact You Will Make: Transform Lives Through Inn ... More
  • 19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1735
    Friday, June 27, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make This is a great opportunity at our Northridge location as a Buyer to purchase materials, supplies and services at the most favorable terms for the organization. This individual will work with vendors, evaluate bids, and negotiates prices and terms for purchased goods and services.  Responsibilities ERP (D365) proficiency and understanding o ... More
  • 11200 Hudson Rd, Woodbury, MN 55129, USA ● Req #1849
    Thursday, June 26, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.  The Impact You Will Make This is a great opportunity to support our Project Managers by handling administrative tasks, ensuring projects stay on schedule and within budget, and facilitating communication and collaboration among team members and stakeholders.  This role will have responsibility for organizing and maintaining project documentation, including project p ... More
  • 19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1965
    Monday, June 23, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The Supervisor, Quality Operations, is responsible for overseeing daily quality operations in compliance with cGMP regulations, company policies, and industry standards. This role ensures the effective execution of quality-related activities, including batch record issuance, quality presence on the floor, batch record review, and product/lot ... More
  • Bridgeton, MO, USA ● Req #1711
    Monday, June 23, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make The mission of Controls - Vision Engineer is to provide highly effective automation, manufacturing workflow solutions, and information collection and reporting for the St. Louis facilities. Our Bridgeton site is a state-of-the-art facility. This individual will provide automation troubleshooting expertise/guidance for corrective maintenance a ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1959
    Thursday, June 19, 2025
    Our Work Matters: At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   Role Overview: We are excited to announce we are expanding our team.   In this role you will be joining our pharmaceutical production line in a controlled environment, working safely and in line with the highest standards of cGMP to meet agreed production schedules.   Working as part of team responsible for running an inhalation production line, full training on a ... More
  • 11200 Hudson Rd, Woodbury, MN 55129, USA ● Req #1953
    Thursday, June 19, 2025
    ROLE SUMMARY The person hired for the position of pMDI Product Development Scientist will support the development and testing of pMDI pharmaceutical products from early development through final submission of regulatory dossiers. This is an exciting role within an expanding team of process and product development specialists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products by applying their creative technical ... More
  • 11200 Hudson Rd, Woodbury, MN 55129, USA ● Req #1952
    Thursday, June 19, 2025
    ROLE SUMMARY The person hired for the position of pMDI Product and Process Development Scientist I will support the development and testing of pMDI pharmaceutical products. This is an exciting role within an expanding team of process and product development specialists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products. ROLE RESPONSIBILITIES Ensure world-class safety within the laboratory and Kindeva Headq ... More
  • 11200 Hudson Rd, Woodbury, MN 55129, USA ● Req #1961
    Thursday, June 19, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make This is an exciting opportunity as a Project Manager, Global Lab Services at our Woodbury location. This role will manage projects from the point of customer engagement to final reporting and confirmation of invoicing. They will follow harmonized robust processes for growth in our global Analytical Services organization. The Project Manageme ... More
  • Bridgeton, MO, USA ● Req #1705
    Thursday, June 19, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make This is an exciting opportunity as a Senior Capital Project Engineer role in Bridgeton facility. This position will assume a leadership role to manage projects in support of the development/implementation of manufacturing processes of new products at the site. In addition, this position will also manage projects to maintain existing Auto Inje ... More
  • 19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1969
    Thursday, June 19, 2025
    Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   The Impact You Will Make The Quality Assurance Auditor (Specialist) demonstrates expertise in core areas of auditing techniques, and considerable knowledge of pharmaceutical, medical device, and combination product regulations and Data Integrity principles. They are responsible for leading the inspection readiness program, planning for internal and external audits, ... More