is preferred. Education Associate's Degree in Microbiology, Biochemistry, Biotechnology, Chemistry, or a related LifeSciences...
Summary Operates and supports packaging equipment for filling, labeling, packing, and wrapping products. Follows Batch Records and cGMP guidelines while maintaining accurate documentation, clean rooms, and safe operations. Key Responsi...
-on experience with Veeva platforms Pharmaceutical / LifeSciences industry experience Experience with data migration projects...
Job Summary: We are seeking a skilled Manufacturing Test Engineer to support testing, validation, equipment setup, and process development activities within a regulated manufacturing environment. The ideal candidate will have experience s...
Roles & Responsibilities: Software Development Lifecycle (SDLC) per DO-178C DAL A Safety Critical Standards Software Requirement Capture & Analysis Software Architecture & Design Traceability Updating Source Code to DO-178C SDLC Revi...
Job Summary The FPA – Shipping/Warehouse role supports logistics operations by managing the receipt, storage, dispensing, and shipment of API and consumable materials. The position involves working with systems such as SAP, Syncade, and s...
Roles & Responsibilities: Software Development Lifecycle (SDLC) per DO-178C DAL A Safety Critical Standards Software Requirement Capture & Analysis Software Architecture & Design Traceability Updating Source Code to DO-178C SDLC Revi...
/external audits. Education & Experience: Bachelor's or Master's degree in Engineering, LifeSciences, Pharmaceutical... Sciences, or a related technical discipline. Minimum 5+years of experience in commissioning, qualification...
Summary : Seeking a Senior Quality Engineer with strong MDR remediation and medical device manufacturing quality experience to support compliance, validation, and risk management activities for regulated product families. Roles & Respon...
Job Summary: Quality Engineer II with experience in medical device manufacturing, process validation, and quality systems compliance within FDA-regulated and EU MDR environments. Skilled in IQ/OQ/PQ validation, process characterization, P...