Responsibilities: Lead part qualification activities by driving the APQP/PPAP process, evaluating and validating supplier manufacturing processes to ensure the delivery of high-quality, cost-effective, and reliable parts that meet design ...
Summary : The Quality Engineer is responsible for maintaining quality and control of manufacturing processes and post-market performance of medical devices. Responsibilities include collaborating with internal and external stakeholders to...
Responsibilities: Manage end-to-end delivery of data management services concurrently for single/multi-service projects with little-to-no guidance, ensuring quality deliverables on time and within budget to customer satisfaction Provide ...
Summary Proficiency in CAD (SolidWorksPTC Creo), GDT, tolerance analysis, and fixture design. Strong capability in test protocol report writing, statistical analysis (9595, tolerance intervals), and data integrity practices. Familiarity...
Role Overview: The Product Quality Engineer (PQE II) will support product engineering and the Quality Management System, leading investigations, supporting change controls, and ensuring compliance with FDA, ISO, and internal quality system...
and stakeholder communication skills Education: Bachelor's or advanced degree in Chemistry, Pharmaceutical Sciences, or related...
Job Description: Regulatory Affairs Specialist II with working knowledge of FDA, and CE marking requirements for IVD products. Client is currently transitioning from IVDD to IVDR (In Vitro Diagnostic Regulation). The RAS is responsible for...
: Bachelor's degree or higher in Statistics, Computer Science, Mathematics, LifeSciences, or a related discipline. 5...
and stakeholder communication skills Education: Bachelor's or advanced degree in Chemistry, Pharmaceutical Sciences, or related...
: Bachelor's Degree in lifesciences or engineering, or other technical discipline. 3-5+years in the pharmaceutical...