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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. Role Overview: This role is joining our dynamic team in Manufacturing Technology (Process & Manufacturing Engineering) where you will be supporting the production and assembly of complex precision components for pulmonary/inhalation drug delivery devices. In this role you will lead the projects/requests for quotation, simultaneously at Kindeva and Kindeva suppl ...Read more about Senior 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 Analytical Scientist required to support multiple R&D activities in Union City. This is a key role within an expanding team of formulation and product development scientists and offers the successful candidate an opportunity to make a significant contribution to the development of new inhalation products ...Read more about Analytical ScientistMore
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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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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 inspection, assembly and packaging product manufacturing equipment qualification/validation, process validation protocols, computer systems validation, and performs testing. The engineer generates validation protocols using templates and is responsible for protocol execution of ...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 The Validation Engineer will assist in the development of inspection, assembly and packaging product manufacturing equipment qualification/validation, process validation protocols, and performs testing. The engineer generates validation protocols using templates and is responsible for protocol execution of various types of basic processing eq ...Read more about 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 The compliance team is responsible for quality compliance improvement within the value stream. The Compliance Engineer will provide technical support to the Inhalation value stream focusing on driving compliance and improving processes. Role Responsibilities Documentation management for manufacturing including reviews of completed batch reco ...Read more about Compliance 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. Role Overview: This is a fantastic opportunity for an engineer who thrives on variety, solving problems, and wants to grow their career within a company that values innovation, teamwork, and continuous improvement. This vital role, where you will use your knowledge and experience to troubleshoot and repair a wide range of complex machinery and systems, join ...Read more about Plant 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 the Supervisor of QC Microbiology – Environmental Monitoring, you will lead a team dedicated to contamination control and quality assurance in our cleanroom environments. Your leadership will be instrumental in maintaining high standards for microbiological monitoring, supporting critical batch and routine testing, and driving qualific ...Read more about Supervisor, QC MicrobiologyMore
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19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1948Monday, June 9, 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 The Senior Complaint Specialist will provide technical leadership and subject matter expertise for the complaints department. This role will focus on overseeing complaint investigations, as well as assisting with metric tracking, complaint trending, complaint reviews including reviewing for potential regulatory reporting, and the issuance and ...Read more about Senior Complaint SpecialistMore
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19901 Nordhoff St, Northridge, CA 91324, USA ● Req #1819Friday, June 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 The Supply Chain Master Planner is responsible for developing and executing strategic supply chain plans that optimize inventory, production, and demand planning. This role ensures alignment with business objectives by integrating APICS principles, managing inventory effectively, and overseeing the Material Review Board (MRB) process to driv ...Read more about Supply Chain Master PlannerMore
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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 This is an exciting opportunity at our new state-of-the-art facility performing validation activities and process transfer as a member of the technical operations team, supporting the contract manufacturing business unit. The candidate will primarily be responsible for supporting multiple technical transfer projects for the aseptic fill and f ...Read more about Senior Manufacturing EngineerMore
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Bishop Meadow Rd, Loughborough LE12, UK ● Req #1942Thursday, June 5, 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 be responsible for managing and coordinating capital projects with a strong focus on mechanical aspects and packaging design. You will lead projects at your assigned manufacturing site and, by exception, other sites as appropriate driven by the project portfolio. Additionally, you will be responsible for providing ...Read more about Senior Capital Project Engineer, Mechanical PackagingMore
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Virtual ● Woodbury, MN, USA ● Req #1654Thursday, June 5, 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 The Senior Director, Quality, Analytical Services is a pivotal leadership position within Kindeva’s Analytical and Development Services (ADS) business unit, overseeing quality operations across the organization. This role is responsible for driving enterprise-wide quality strategy, ensuring compliance with regulatory requirements, and fosteri ...Read more about Senior Director-Quality, Analytical ServicesMore
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St. Louis, MO, USA ● Req #1944Thursday, June 5, 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 This position is accountable for: Serving as EHS point of contact for potential new product introductions, tech transfer activities to achieve production readiness. This includes: providing EHS expertise and inputs in support of bench-scale process development and high potent chemical banding alignment assist with supporting current o ...Read more about Environmental Health and Safety Project Manager and Technical TransferMore
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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 Device (QCD) Manager will be primarily based in the Maryland Heights Manufacturing building and will provide general oversight to the QCD Laboratories. The QCD Manager develops, directs and leads the QC Device testing laboratory, supporting the testing of incoming components (packaging materials, preassembled components, ...Read more about Quality Control Device ManagerMore
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11200 Hudson Rd, Woodbury, MN 55129, USA ● St. Louis, MO, USA ● Req #1791Wednesday, June 4, 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 This individual will be responsible for the Treasury function at Kindeva. In this highly visible role, you will update cash forecasting each week for the management team and PE sponsors. You'll use that forecast to make good decisions around transferring funds and borrowing. As the chief fiduciary of the company's cash, you'll also adminis ...Read more about Treasury ManagerMore
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Bridgeton, MO, USA ● Req #1768Wednesday, June 4, 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 be responsible for overseeing the quality of equipment and material preparation, as well as aseptic compounding, filling, and inspection activities. Supporting site-wide objectives, you will coordinate support activities, review and audit semi-finished product manufacturing and testing documentation, and ensure that al ...Read more about Integrated Quality Assurance Inspector - 2nd ShiftMore
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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 ...Read more about Regulatory Affairs SpecialistMore
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Bishop Meadow Rd, Loughborough LE12, UK ● Req #1910Sunday, June 1, 2025Our 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 ...Read more about Senior QC Investigations AnalystMore
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St. Louis, MO, USA ● Virtual ● Woodbury, MN, USA ● Req #1762Thursday, May 29, 2025OUR 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 ...Read more about Contracts Specialist - CDMOMore
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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 ...Read more about Manufacturing Team Lead - Second ShiftMore
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Validation Engineer 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-rea ...Read more about Sr. 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 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 ...Read more about Corporate ParalegalMore
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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. 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 ...Read more about Maintenance 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 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 ...Read more about Senior Manufacturing Engineering IIMore