Responsibilities: Create and support review of validation life cycle documents for Analytical Instrument Qualification and computerized systems. Experience in validation of anal…
Job Description: We are looking for a Finishing Area Support Associate to assist with product finishing activities, including component screening, kit assembly, and preparing pack…
Job Description: We are seeking a Product Development Tech for our Brea, CA facility. This person contributes to the completion of routine technical tasks and develops solutions t…
Responsibilities: The statistical programming contractor independently manages completed projects that involve global tasks, or cross functional teams. The role may require prov…
Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of internatio…
Roles & Responsibilities: With minimal guidance, the principal engineer schedules, interfacing with development groups and technical support groups. The principal R&D engineer d…
Job Description: The chart review is critical, and the candidate must have knowledge of reviewing medical records for disease process, hanging blood and IV lines as well as critic…
Job description: Supports the activities and initiatives of Convergence Governance team to implement and manage the Governance Risk Assessment activities including its policies, p…
Roles & Responsibilities: Bachelor's degree in computer science, Information Technology, Electronics Engineering, or a related field. Minimum 5-8 years of experience in software…
Responsibilities: Execute movement of finished goods utilizing scanner or digital device. Transfer of Finished Product. Delivery of Isopropyl Alcohol. Delivery of Miscellaneou…
Job Description: Provide lab IT support, consulting, validation/compliance services, and troubleshoot multivendor lab instruments & systems. Work closely with business users, lab …
Responsibilities: Well versed with Manufacturing, Quality and engineering system and their validations. OT System Qualification (Radio ligand Therapy or critical dosage forms wi…
Responsibilities: Knowledge of application of Regulatory requirement including ISO 13485, FDA and International requirements. Enhanced quality system requirements (QSR) througho…
Responsibilities: Drive validation activities across the product lifecycle, including IQ/OQ/PQ protocol development and execution. Apply APQP methodologies to support new produc…
Responsibilities: Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data throu…
Job Description: Manual Protocol Tester to support software verification activities for web-based applications integrated with heart failure/ medical devices. The ideal candidat…
Job description: Should have hands on experience in EDC-Medidata Rave / any other clinical EDC system clinical database & setting up EDC-Veeva CDMS/Medidata RAVE studies and prog…
Job Description: We are seeking a Change Management & User Experience Specialist to partner with the Associate Director, Procurement User Experience in driving successful adoption…
Roles & Responsibilities: Bachelor's degree in computer science, Engineering, Life Sciences, or related field. 3-7 years of experience in CSV within pharmaceutical, biotech, or …
