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Company Description
Kyro BioPharma Solutions is a specialized recruitment and contract employment partner for FDA-regulated industries, uniting engineering, technical, and scientific talent to advance critical projects with precision and speed. Headquartered in New Hampshire and active across New York, Pennsylvania, North Carolina, Florida, and New Jersey, the firm supports clients in pharmaceuticals, biotechnology, cell and gene therapy, medical devices, and CRO/CMO/CDMO environments. Kyro delivers managed staffing programs, contract consultants, and direct hire solutions that keep operations compliant and productive from lab to commercial manufacturing. Its project scope spans CAPEX project execution; commissioning, qualification, and validation (CQV); automation and controls; MES and CSV; process engineering; manufacturing science and technology (MSAT); operations management; factory and site acceptance testing (FAT/SAT); and comprehensive QMS and GMP remediation. The team routinely assembles project-based teams and places individual contributors including validation and automation engineers, QA/RA and compliance specialists, CAPA investigators, construction project managers, facilities and site engineers for HVAC, cleanrooms, and utilities, technical writers and SOP experts, as well as project controls and scheduling professionals. Clients choose Kyro for regulatory depth, tailored delivery, and market-best pricing, trusting an approach that integrates risk mitigation, quality assurance, and operational efficiency to accelerate timelines without compromising safety or compliance. Candidates gain access to flexible consulting engagements and long-term roles that contribute to safer, more effective therapies and devices, with opportunities aligned to emerging guidance and evolving quality expectations across FDA-regulated sectors. Whether expanding API capacity, remediating inspection findings, scaling a new line, or modernizing manufacturing with digital and automated systems, Kyro BioPharma Solutions aligns specialist talent to measurable outcomessustaining compliance, optimizing throughput, and ensuring readiness for audits and submissions while supporting the continuous advancement of global health.
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