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Bishop Meadow Rd, Loughborough LE12, UK ● Req #1766Wednesday, April 16, 2025Our 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 ...Read more about Senior Capital Project EngineerMore
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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 ...Read more about Engineering Project ManagerMore
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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 Quality Assurance Specialist, you will play a vital role in safeguarding product integrity, ensuring regulatory compliance, and driving a culture of quality across the organization. Your contributions will directly impact patient safety, product reliability, and the overall success of our mission to deliver high-quality pharmaceutica ...Read more about Quality Assurance Specialist IIMore
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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 ...Read more about Senior Validation EngineerMore
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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 be responsible for auditing aseptic processes to ensure compliance with established specifications, procedures, cGMPs, and FDA regulations, while identifying any non-conformances. You will need strong written and verbal communication skills, as well as the ability to collaborate effectively across multiple department ...Read more about QA Inspector - 3rd ShiftMore
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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 Systems Supervisor plays a critical role in driving quality and compliance across the organization, directly impacting the success of our CDMO operations. By leading key quality systems, particularly CAPA management, audit hosting, supplier quality oversight, and annual product quality reviews, this individual ensures continuo ...Read more about Sr. Supervisor, Quality SystemsMore
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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 successful candidate will ensure products, processes and equipment comply with quality standards and regulations by leading a team of validation engineers and overseeing the validation activities, including testing, documentation, and compliance with cGMP and regulatory requirements for the entire lifecycle within the assigned site. Rol ...Read more about Validation ManagerMore
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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 Control Lab Technician engages in statistical sampling, inspection and physical testing of incoming materials for conformance to approved written specifications, Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), and Food and Drug Administration (FDA) regulations. Typical hours for this role are: ...Read more about Quality Control Lab TechnicianMore
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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 pharmaceutica ...Read more about Senior Process EngineerMore
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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: Transform Lives Through Innovation As ...Read more about Supplier Process Engineer IIMore
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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 develop, direct, and lead Quality oversight for process improvements in equipment and material preparation, aseptic compounding, filling, inspection, and packaging at the Brentwood, Maryland Heights, and Bridgeton facilities. You will coordinate support activities, reviews, audits, and the release of semi-finished prod ...Read more about Quality EngineerMore
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Lexington, KY, USA ● Req #1777Tuesday, April 1, 2025Our 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: Transform Lives Through Innovation Joi ...Read more about Senior Environmental, Health, Safety & Security SpecialistMore
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Lexington, KY, USA ● Req #1568Monday, March 31, 2025Our 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 be responsible for performing maintenance and calibration activities in a pharmaceutical cGMP manufacturing facility and supporting the manufacturing of life-changing and life-saving prescriptio ...Read more about Maintenance and Calibration Technician - 2nd ShiftMore
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Lexington, KY, USA ● St. Louis, MO, USA ● Virtual ● Woodbury, MN, USA ● Req #1781Thursday, March 27, 2025Our 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, oversee strategic sourcing and supplier management for the chemical category (Active pharmaceutical ingredients, excipients, gases, propellants, etc), ensuring alignment with business goals, compliance with regulatory standards, and cost efficiency. This role requires expertise in category management, supplier relations ...Read more about Category Manager - Direct Procurement, ChemicalsMore
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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 Supply Chain Director is responsible for leading the strategic direction of the Supply Chain functions and activities within the Injectables & Global Health Security Business Unit, accountable for Sales & Operations Planning and Sales & Operations Execution; demand Planning and Scheduling; Warehouse, Logistics and Distribution; ass ...Read more about Sr. Director, Supply Chain & LogisticsMore
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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 lead all finance and accounting functions for Kindeva’s St. Louis drug and device manufacturing operations. You will support the Site GM/VP in strategic decision-making, oversee standard costing, financial reporting, month-end closes in compliance with US GAAP, and assist with audits. Additionally, you will manage b ...Read more about Senior Finance DirectorMore
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Bridgeton, MO, USA ● Req #1721Thursday, March 6, 2025Our 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 as the Director of Technical Transfer, Product & Process Technology (“Tech Transfer”) you are responsible for engineers, scientists, and technical professionals with expertise in aseptic/ sterile drug product formulation, vial, syringe and cartridge filling, inspection and primary packaging manufacturing activities for liquid, l ...Read more about Director, Technical Transfer and Process TechnologyMore
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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: Transform Lives Through Innovation Joi ...Read more about Manufacturing ManagerMore
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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 be responsible for auditing aseptic processes to ensure compliance with established specifications, procedures, cGMPs, and FDA regulations, while identifying any non-conformances. You will need strong written and verbal communication skills, as well as the ability to collaborate effectively across multiple departments ...Read more about Technical Transfer Process LeadMore
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Bridgeton, MO, USA ● Req #1613Friday, January 10, 2025Our 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 drive strategic alignment with the vision and operational plans to achieve site and business objectives while adhering to regulatory and Kindeva standards without compromising quality, compliance, or values. You will provide clarity, alignment, and direction to your team, partnering cross-functionally to develop and execu ...Read more about Senior Director, Aseptic Manufacturing OperationsMore
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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. Ready to work with purpose? Look no further, we are hiring for a motivated, talented, and passionate Sr. Manufacturing Engineer to join our St. Louis Missouri team! The Sr. Manuf ...Read more about Sr. Manufacturing EngineerMore
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Clitheroe BB7, UK ● Columbia, MD, USA ● Loughborough LE12, UK ● Northridge, Los Angeles, CA, USA ● St. Louis, MO, USA ● Union City, CA, USA ● Woodbury, MN, USA ● Req #1043Monday, December 18, 2023Create your career profile by completing this general application. Stay in touch regarding opportunities to combine forces with us in manufacturing more tomorrows. ...Read more about JOIN OUR TALENT COMMUNITYMore