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Responsible for supporting QC Critical Materials, Reference Standards, and procurement of laboratory materials at the Limerick Manufacturing site. Duties include purchasing, managing orders, evaluating completeness and accuracy, checking inventory levels, and supporting project work within the group.
Provide administrative support and coordination to Senior Vice President and Senior Staff in the Global Patient Safety department at Regeneron. Responsibilities include calendar management, meeting logistics, travel coordination, expenses processing, and technical support. Must have 4-6+ years of relevant administrative experience and a minimum of an Associate or BS/BA degree.
The Global Procurement Associate - Leadership Development Rotational Program at Regeneron is a two-and-a-half-year rotational program designed for recent university graduates. Participants will undergo three distinct rotational roles to gain diverse procurement experiences. Responsibilities include collaborating with stakeholders, analyzing data, negotiating with suppliers, and supporting global procurement efforts. Applicants must have a four-year degree and skills in analytics, organization, communication, and technology.
Join Regeneron as a Process Controls & Validation Engineer in the Process Sciences Drug Product Engineering department. Provide engineering support for designing robust drug product processes and enable global delivery of medications. Collaborate with teams, design unit operations, write protocols, support investigations, and drive process improvements. Travel may be required.
Senior LIMS Developer role at Regeneron supporting the RCM unit in Cambridge, MA. Responsibilities include customizing LIMS, developing data solutions, collaborating with scientists, and supporting IT systems. Requires advanced degree in Computer Science or similar field, 3 years of experience in programming, and expertise in informatics software platforms.
Lead and support programming activities within therapeutic areas, ensuring high-quality results for multiple studies. Provide technical guidance, contribute to regulatory submissions, mentor junior programmers, and collaborate with global teams. Requires proficiency in SAS programming, knowledge of clinical development, and a Master's degree with 8+ years of experience.
Manage Global Price Management System, conduct pricing analytics, provide recommendations to stakeholders, generate pricing reports, and support Global Pricing Committee. Requires 5+ years of experience in Market Access / Pricing in Pharma or Biotech sector.
Regeneron is seeking a QC Micro Specialist to develop new QC microbiology test methods, provide critical microbiology support, and ensure departmental compliance. Responsibilities include leading test method verifications, implementing verified methods, authoring protocols and reports, troubleshooting microbiological assays, collaborating on change control activities, and participating in internal audit discussions.
Senior IT Operations Specialist responsible for managing service providers, ensuring high service availability and efficiency, maintaining operational support functions, and driving service and support in operational projects. Requires strong experience in Infrastructure Operations, knowledge of IAAM, QAR, CyberArk, and SailPoint tools, and proficiency in ITIL disciplines.
The Quality Control Analyst at Regeneron performs routine testing of drug samples, provides support to the manufacturing process, assesses data for product specification compliance, conducts investigations of test results, and maintains lab inspection readiness.
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