The candidate will work as part of a collaborative, chemical process development team with a range of responsibilities including organic synthesis, reaction characterization & optimization, kinetics studies, distillations, crystallizations,...
The Site Engineer is responsible for overseeing the maintenance, calibration, operational readiness of equipment, utilities, and facilities supporting cGMP manufacturing and laboratory areas. This role is integral to ensure the efficient, r...
This position is responsible for all aspects of Chemistry, Manufacturing, and Controls (CMC) drug product development from early stage to late-stage clinical development and commercialization, including development of efficient and scalable...
Our client is seeking a Technology: Organizational Effectiveness (OE) Manager focused on organizational change management and communications. They are looking for a Change Manager who has strong experience supporting enterprise IT transfo...
The Manufacturing Specialist is expected to own and execute under minor supervision all the processes related to deviations (minor and majors), Corrective and Preventive Actions (CAPAs), CAPA-Effectiveness Verifications, Supplier Event Noti...
Join the Business Performance team working in the site's Project Management Office as a program manager, with a specific focus on scheduling and information management. Manage the integration of technical project timelines, risk managemen...
The Senior Director of Medical Writing will have responsibility for executing a fit-for-purpose delivery model to produce a range of high quality clinical and regulatory documents to advance company goals across all investigational and mark...
The Clinical Trial Specialist (CTS) is responsible for providing logistical support for one or more clinical trial programs. This position will work closely with cross-functional teams to ensure site start-up through close-out activities ar...
The Sr. CRA will be responsible for monitoring clinical studies at the site level, ensuring adherence to protocols, timelines, ICH/GCP guidelines, and federal regulations. The Sr. CRA will perform site qualification visits, study start-up a...
Responsibilities: Act as Quality Assurance (QA) contact for Change Control(s) for Computerized System activities Review and Approve validation deliverables (e.g. Validation Plan, Requirement Assessment, support Testing Protocols, Summary...