Job Description: Laboratory Systems Operations (LSO) group is a key study team partner in the lab engagement process and plays a critical role in supporting Client Clinical Trials. For every Client clinical study, LSO assists with the dev...
Responsibilities: The Regulatory Affairs Specialist is responsible for working with cross-functional teams to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality Ma...
Responsibilities: Lead mechanical design efforts using SolidWorks 3D, focusing on sheet metal and casting components. Collaborate with cross-functional teams to develop prototypes and support production ramp-up. Drive Value Analysis/Val...
Job Description: The purpose of the Product Development & Testing position is to complete assignments in support of R&D process development for the commercialization of new medical wire coating applications. The successful candidate will...
Summary: We are seeking a Commissioning Engineer to join one of our largest pharmaceutical clients 5x/week onsite in Rensselaer, NY. This individual will be joining the engineering team within the Engineering and Automation space assistin...
Job Description: Our client is a large medical device manufacturer addressing FDA-driven remediation needs within manufacturing operations. They are seeking an experienced, fully onsite Quality Engineer to support process risk, validatio...
Job Description: The Manufacturing Services Associate I supports cGMP manufacturing production suites by ensuring materials, equipment, and facilities are maintained to compliance standards. This entry-level role involves stocking suites, ...
Responsibilities: Own the end-to-end design of major subsystems and ensure successful integration into full systems. Lead cross-functional design reviews, making trade-off decisions between mechanical, electrical, and software requiremen...
Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets Crea...
The Global Regulatory Affairs (GRA) is responsible for obtaining approval for new products and ensuring that approval is maintained throughout the product lifecycle. GRA serves as the interface between the regulatory authorities and the pr...