Job Details. The ideal candidate will be responsible for developing, executing, and documenting validation strategies in alignment with FDA, EMA, and ICH Q7–Q10 guidelines. The role focuses primarily on commissioning and qualification (C&Q) of GMP equipment, utilities, and facility systems to ensure regulatory compliance and operational readiness. E. Employers have access to artificial intelligence language tools (“AI”) that help generate and enh...
Job Details. We are seeking a technical contractor to support a file share migration project. The objective is to move files from an on-premises file share to cloud-based storage, such as SharePoint Online or Azure Hot Storage. Key Responsibilities. Assess the current file share environment to identify documents containing embedded links. Provide input into a detailed migration plan based on the scope and complexity of embedded link dependencies....
Job Details. Senior GxP IT Consultant. . The Senior GxP IT Consultant will be responsible for working cross-functionally and collaboratively with outside vendors on GxP specific systems support. . 10 years of relevant experience supporting GxP projects. Location: MA or EST Contract Duration: 1 Year Contract Rates: $ 60/ph. Key Responsibilities. Configure elluminate® environments, modules, roles/permissions, and support compliant Release. Manageme...
Job Details. Job Summary. We are seeking an experienced Senior MES (Manufacturing Execution Systems) Solutions Consultant to join our team on a contract basis. This role emphasizes strategic expertise in identifying operational gaps and developing innovative solutions within MES environments, rather than hands-on validation execution. Our client utilizes Syncade as their MES platform, but direct experience with this specific system is not require...
Job Details. What I m looking for. Experience with PLCs, HMIs, SCADA, MES, OSI PI, DeltaV, Rockwell, Siemens, Ignition. Strong understanding of regulated manufacturing processes. Hands-on involvement in commissioning, validation, and system integration. Familiarity with industrial protocols like Modbus, Profibus, and Ethernet/IP. These roles offer the chance to work on cutting-edge projects in pharma manufacturing and R&D from greenfield builds t...
Role Description. This is a contract role for a Process Quality/Validation Engineer. The day-to-day tasks include ensuring compliance with Good Manufacturing Practice (GMP), performing validation and functional verification, and troubleshooting or debugging issues as they arise. The engineer will work on RTL design and validation processes. This role is on-site and is located in Boston, MA. Qualifications. 1 year's of experience required. Knowled...
