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  • Lexington, KY, USA ● Req #1876
    Tuesday, June 3, 2025
    Regulatory Affairs Specialist (Lexington, KY Site) Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Our Work MattersAs a Regulatory Affairs Specialist at Kindeva, your role is essential to ensuring our products remain compliant, safe, and accessible to patients worldwide. From managing licenses and technical documentation to supporting regulatory strategy and site activities, your work helps maintain the integrity ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1910
    Sunday, June 1, 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 seeking a highly skilled and detail-oriented Senior QC Investigations Analyst to join our Quality Control (QC) team. In this critical role, you will lead and manage a variety of laboratory investigations, ensuring compliance with Good Manufacturing Practice (GMP) and company quality standards. Apply your analytical expertise to identify root ... More
  • St. Louis, MO, USA ● Virtual ● Woodbury, MN, USA ● Req #1762
    Thursday, May 29, 2025
      OUR WORK MATTERS At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. ROLE SUMMARY This role will serve as a Contracts Specialist for a life sciences contract development and manufacturing organization. With significant changes in the marketplace, Kindeva is currently going through a period of substantial growth, and we are looking for talented individual to join our Legal team.  ROLE RESPONSIBILITIES Responsibilities inclu ... More
  • Lexington, KY, USA ● Req #1891
    Friday, May 23, 2025
    Manufacturing Team Leader (Lexington Site) 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 ... More
  • Lexington, KY, USA ● Req #1920
    Friday, May 23, 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 Validation Engineer, you will play a critical role in ensuring our pharmaceutical manufacturing systems and processes meet rigorous regulatory and quality standards. You will lead and execute validation activities—including equipment, utilities, facilities, and process validations—to ensure our operations remain compliant and inspection-ready. Your expertise in ... More
  • St. Louis, MO, USA ● Req #1864
    Wednesday, May 21, 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 Corporate Paralegal is responsible for providing administrative and project support to the Kindeva Legal department. Role Responsibilities Responsible for monitoring and processing company’s state drug distribution licenses ensuring compliance with state regulatory requirements.  Responsible for monitoring and processing annual business ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1895
    Thursday, May 15, 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 seeking Maintenance Engineers to join our growing team.   In this role you will perform both planned preventative maintenance (PPM) and reactive maintenance on manufacturing, production and process equipment in accordance with GMP standards working across our Loughborough sites. You will work flexibly to meet business demands, workin ... More
  • Lexington, KY, USA ● Req #1902
    Thursday, May 15, 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 Sr. Manufacturing Engineer II, you will play a critical role in driving manufacturing excellence through process optimization, equipment innovation, and cross-functional collaboration. By leading initiatives that enhance productivity, quality, and compliance, you will directly contribute to improved operational performance and product ... More
  • Lexington, KY, USA ● Req #1901
    Thursday, May 15, 2025
    Sr. Automation Engineer 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 Automation Engineer, you will play a vital role in designing, implementing, and maintaining automated systems to support pharmaceutical manufacturing in a cGMP environment. Your expertise will drive efficiency, improve equipment performance, and enhance product reliability. This role combines hands-on technica ... More
  • St. Louis, MO, USA ● Req #1912
    Thursday, May 15, 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 Supplier Quality Engineer’s primary responsibility is to manage assigned supplier relationships and quality program deliverables. Provides oversight, evaluation, and corrective action of all production and supplier quality related issues for external supplier processes and suppliers based on commodity class assigned. Generates reports, me ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1908
    Wednesday, May 14, 2025
    Our Work Matters:   At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.   Overall Mission:   To undertake pharmaceutical production line operator duties, working safely and in line with the highest standards of cGMP to meet agreed production schedules.   Role Overview:   You will work as part of team responsible for running an inhalation production line to ensure production targets are met.  You will be given training in the departmen ... More
  • St. Louis, MO, USA ● Req #1587
    Tuesday, May 13, 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 Manufacturing Process Engineer plays a crucial role in ensuring consistent high performance of manufacturing equipment and processes. This “hands on” position owns the manufacturing process and focuses on the performance of manufacturing operations to ensure quality, improve performance and reduce line scrap / waste.     Essential Job Fun ... More
  • Maryland Heights, MO, USA ● Req #1327
    Tuesday, May 13, 2025
    Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows. ROLE SUMMARY The Manufacturing Process Engineer plays a crucial role in ensuring consistent high performance of manufacturing equipment and processes. This “hands on” position owns t ... More
  • Bridgeton, MO, USA ● Req #1806
    Saturday, May 10, 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 In this role you will support the technical transfer activities of client projects by developing manufacturing instructions, creating process flow diagrams, analyzing process data for trends and inclusion to reports, and providing training. Role Responsibilities • Develop easily understood production instructions based on the client manufact ... More
  • Lexington, KY, USA ● Req #1880
    Friday, May 9, 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’re looking for a role with purpose, join our team and help support the manufacturing of life-changing medications. As a Warehouse Associate, you’ll play a critical role in ensuring materials and inventory are handled with precision and care in a GMP-regulated environment—supporting pharmaceutical production that direct ... More
  • Lexington, KY, USA ● Req #1879
    Friday, May 9, 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’re looking for a role with purpose, join our team and help support the manufacturing of life-changing medications. As a Warehouse Associate, you’ll play a critical role in ensuring materials and inventory are handled with precision and care in a GMP-regulated environment—supporting pharmaceutical production that directl ... More
  • Brentwood, MO, USA ● Req #1843
    Wednesday, May 7, 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 In this role, you are responsible for leading the aseptic filling operations and technical services within the Brentwood sterile injectable filling facility. The primary duties are to assure operational success and drive best-in-class capabilities, and performance related to safety, quality, compliance, and operational execution. Scope of re ... More
  • St. Louis, MO, USA ● Req #1859
    Friday, May 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 Senior Buyer is responsible for procuring direct and indirect materials essential to pharmaceutical manufacturing operations, ensuring timely supply to support production, quality, and compliance. This individual evaluates and selects suppliers based on cost, quality, and regulatory standards, and supports supplier diversity by ensuring c ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1794
    Thursday, April 24, 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:   This role sits within the Kindeva Outsourced Manufacturing Team, which supports the commercialized IDD Devices, providing basic technical / non-technical support to Outsourced partners, customers, and internal colleagues. The main device is the integrated dose counter/ dose indicator inserted into an actuator to deliver inhaled respiratory medic ... More
  • Lexington, KY, USA ● Req #1787
    Wednesday, April 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: 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 tea ... More
  • Lexington, KY, USA ● Req #1839
    Wednesday, April 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: 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 tea ... More
  • Lexington, KY, USA ● Req #1840
    Wednesday, April 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: 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 tea ... More
  • Bishop Meadow Rd, Loughborough LE12, UK ● Req #1766
    Wednesday, April 16, 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: As Senior Project Engineer you will take responsibility for providing safe and compliant delivery of assigned capital projects, on time, within budget and to the agreed scope. You will lead projects at your assigned manufacturing site and, by exception, other sites as appropriate driven by the project portfolio. In this role you will utilise your kn ... More
  • Lexington, KY, USA ● Req #1827
    Wednesday, April 16, 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 Project Manager – Engineering, you will lead cross-functional teams to successfully deliver critical engineering and validation projects that directly support operational excellence, innovation, and compliance. By effectively managing timelines, resources, risks, and budgets, you’ll ensure projects are executed with precision and trans ... More
  • Bridgeton, MO, USA ● Req #1712
    Thursday, April 10, 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 Senior Validation Engineer will assist in the development of Aseptic product manufacturing equipment qualification/validation, Cleaning Validation, Process validation, computer systems validation, perform testing and write validation reports.  This individual will generate validation protocols using templates and be responsible for protoc ... More