Roles and Responsibilities: 4+years' experience in a medical device manufacturing environment. Strong preference for assembly automation systems experience. Validation experience: IQ, OQ, PQ and TMVs Automation control systems ba...
's degree in Engineering, LifeSciences, or related field;advanced degree preferred. Minimum of 5 years of experience in CQV...
Responsibilities: Prioritize timely completion and remediation of Corrective Action and Preventive Action (CAPA) - performing investigations, corrections, corrective actions, preventive actions and effectiveness checks. Perform review an...
Description: looking for a candidate with experience in Clinical Data Management and Biostatistics departments. Focuses on Incident, Problem, and Change is responsible for the ownership and management of these processes Lead major incid...
Responsibilities: Evaluates customer complaints, including the coordination of documentation review, sample testing, and root cause analysis. Leads and/or facilitates the compliant investigation to reduce or eliminate causes of the compl...
Responsibilities: Provide quality assurance oversight for C&Q, verification, and validation activities, ensuring compliance with GMP, FDA, and other regulatory requirements. Collaborate with engineering, operations, and IT teams to ensur...
Responsibilities: Support the initiatives of the Quality Assurance department Supply chain support in the development and maintenance of a supplier rating system and supplier evaluation Develop and provide statistical analysis of qualit...
Roles & Responsibilities: 2+in Years in Medical Device Industry. Lead and or support early innovation / proof of concept development work. Develop 3D CAD models using Solidworks or similar CAD modelling platforms. With guidance f...
needed. They will be responsible for the full life cycle of the CAPA from root cause analysis, to writing the investigation...
guidance and support to site quality teams in process implementation. Requirements: Bachelor's degree in LifeSciences...