Responsibilities: Ensure departmental or functional training plans in place and appropriate Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deli...
Job Summary: We are looking for an NPD Engineer (Medical Device) to support long-term onsite projects in Irvine, CA. The role involves new product development activities, project coordination, cross-functional collaboration, and supporti...
Job Description: Responsible for supporting the manufacturing and assembling clinical and commercial products including lab maintenance, file maintenance, and support in creating materials for batches to meet specifications. Responsibilit...
Summary : We are seeking an experienced Quality Engineer, who you will be one the key on-site points of contact for quality issue management. The Quality Engineer is responsible for qualification, triage, management and dispatch of incomi...
Summary: We are hiring Supplier Quality / Packaging Engineers to support compliance with the EU Packaging & Packaging Waste Regulation (PPWR), effective August 12, 2026. This role plays a critical part in ensuring that all packaging for E...
Roles & Responsibilities: Experience in interacting with Global vendors & doing site visits across US Experience in drafting Incoming Inspection procedures First Article Inspection & Qualification Good experience in Test method develop...
integrity, shelf life, and transit testing. Mandatory: Medical Device Industry....
Roles & Responsibilities: Testing and Validation. Plan and conduct functional tests and performance evaluations on hardware prototypes. Identify and troubleshoot issues related to hardware functionality and compatibility. Collaborate w...
Job Summary: The CQV Automation Engineer is responsible for executing and documenting automation commissioning, qualification, and testing activities within a GMP biotech or pharmaceutical manufacturing environment. This role supports au...
including IEC 62304 (software life cycle), ISO 14971 (risk management), and FDA medical device software guidance....