Kindeva Drug Delivery
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 Supply Chain Specialist I, you will be responsible for managing and optimizing end-to-end supply chain processes for pharmaceutical products-from raw materials and intermediates to finished goods. Your role will ensure the timely, compliant, and efficient delivery of materials to support manufacturing, development, and commercial operations.
By collaborating with internal stakeholders, external suppliers, and contract manufacturing organizations, you will strengthen supplier partnerships, resolve complex supply chain challenges, and drive continuous improvement. With your expertise in GMP/GDP regulations, ERP systems, and cross-functional project leadership, you will contribute directly to seamless operations and the successful delivery of life-changing treatments.
Growth Opportunity
Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions.
Responsibilities: Drive process optimization for D365 (ERP System). Coordinate and oversee Corrective and Preventive Actions (CAPA) related to supplier quality events, vendor complaints, and change management activities. Manage commercial client relationships and ensure on-time, in-full (OTIF) delivery performance. Collaborate with Manufacturing, Quality, Regulatory, and R&D to align supply chain activities with business objectives. Manage supplier and CMO relationships, including raw material sourcing and performance monitoring. Resolve supply disruptions, shipment delays, and quality issues with vendors. Oversee inbound and outbound logistics, including cold chain and controlled substances. Ensure compliance with GMP, GDP, and company SOPs. Prepare and maintain documentation for audits, inspections, and regulatory submissions. Serve as SME during internal and external audits. Lead or support cross-functional projects (ERP upgrades, serialization, sustainability). Track and report key KPIs for supply chain operations. Assist in budget development and manage service and supplier contracts via ConvergePoint. Qualifications:
Education:
Bachelor's degree in Supply Chain Management, Business, Engineering, Life Sciences, or related field. Experience:
Minimum 6 years of supply chain experience in pharma/biotech (medical device/components preferred). Knowledge of cGMPs, FDA guidelines, ISO and ASTM standards, and global supply chain regulations. Experience with cold chain logistics and temperature-sensitive products. Strong analytical and problem-solving skills; proficiency with Microsoft Excel, Power BI, and supply chain systems. Ability to mentor junior staff and lead cross-functional initiatives. Excellent communication and interpersonal skills; able to manage multiple priorities in a fast-paced environment. Strong understanding of CAPA processes and ability to recommend corrective/preventive actions. Statistical and mathematical skills applicable to supply chain and process analysis. Computer skills: Microsoft Office Suite, Microsoft Project, and statistical software (Minitab, Stat Graphics, PH Stat). Familiarity with supplier and materials processes, ERP systems, and measurement/calibration techniques. Physical/Mental Requirements:
Occasionally required to stand, walk, sit, talk, or hear. Must be able to lift/move up to 35 pounds. Ability to adjust focus; moderate noise level in the work environment. Non-Standard Work Schedule, Travel, or Environment Requirements:
Minimal travel (5-10%) both within the U.S. and abroad. Must manage multiple priorities, meetings, and communications across global teams. Willingness to work beyond typical hours, which may include weekends or holidays, to meet deadlines.
# LI-Onsite
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 Supply Chain Specialist I, you will be responsible for managing and optimizing end-to-end supply chain processes for pharmaceutical products-from raw materials and intermediates to finished goods. Your role will ensure the timely, compliant, and efficient delivery of materials to support manufacturing, development, and commercial operations.
By collaborating with internal stakeholders, external suppliers, and contract manufacturing organizations, you will strengthen supplier partnerships, resolve complex supply chain challenges, and drive continuous improvement. With your expertise in GMP/GDP regulations, ERP systems, and cross-functional project leadership, you will contribute directly to seamless operations and the successful delivery of life-changing treatments.
Growth Opportunity
Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions.
Responsibilities: Drive process optimization for D365 (ERP System). Coordinate and oversee Corrective and Preventive Actions (CAPA) related to supplier quality events, vendor complaints, and change management activities. Manage commercial client relationships and ensure on-time, in-full (OTIF) delivery performance. Collaborate with Manufacturing, Quality, Regulatory, and R&D to align supply chain activities with business objectives. Manage supplier and CMO relationships, including raw material sourcing and performance monitoring. Resolve supply disruptions, shipment delays, and quality issues with vendors. Oversee inbound and outbound logistics, including cold chain and controlled substances. Ensure compliance with GMP, GDP, and company SOPs. Prepare and maintain documentation for audits, inspections, and regulatory submissions. Serve as SME during internal and external audits. Lead or support cross-functional projects (ERP upgrades, serialization, sustainability). Track and report key KPIs for supply chain operations. Assist in budget development and manage service and supplier contracts via ConvergePoint. Qualifications:
Education:
Bachelor's degree in Supply Chain Management, Business, Engineering, Life Sciences, or related field. Experience:
Minimum 6 years of supply chain experience in pharma/biotech (medical device/components preferred). Knowledge of cGMPs, FDA guidelines, ISO and ASTM standards, and global supply chain regulations. Experience with cold chain logistics and temperature-sensitive products. Strong analytical and problem-solving skills; proficiency with Microsoft Excel, Power BI, and supply chain systems. Ability to mentor junior staff and lead cross-functional initiatives. Excellent communication and interpersonal skills; able to manage multiple priorities in a fast-paced environment. Strong understanding of CAPA processes and ability to recommend corrective/preventive actions. Statistical and mathematical skills applicable to supply chain and process analysis. Computer skills: Microsoft Office Suite, Microsoft Project, and statistical software (Minitab, Stat Graphics, PH Stat). Familiarity with supplier and materials processes, ERP systems, and measurement/calibration techniques. Physical/Mental Requirements:
Occasionally required to stand, walk, sit, talk, or hear. Must be able to lift/move up to 35 pounds. Ability to adjust focus; moderate noise level in the work environment. Non-Standard Work Schedule, Travel, or Environment Requirements:
Minimal travel (5-10%) both within the U.S. and abroad. Must manage multiple priorities, meetings, and communications across global teams. Willingness to work beyond typical hours, which may include weekends or holidays, to meet deadlines.
# LI-Onsite