integrity, shelf life, and transit testing. Prepare packaging verification protocols and reports in compliance with regulatory...
Job Summary: Quality Assurance Engineer responsible for providing design assurance support for new product development and on-market medical devices. The role focuses on facilitating design controls, ensuring regulatory compliance, supp...
and inputs from SMEs and project teams. Experience in LifeSciences / Pharma / Biotech. Experience as a Test Lead (Manual...
Roles & Responsibilities: Serve as the subject matter expert for planning, setup, and acquisition of external clinical data at the study level, managing study startup, conduct, and closeout activities. Create external data transfer agree...
Strong understanding of medical device product life cycle and regulatory requirements In-depth knowledge of ISO 13485, FDA regulations...
Science, LifeSciences, or related field. Advanced degree (Master's) preferred but not mandatory. Additional certifications...
Job Description: Responsibility for the Quality and Compliance of process development and manufacturing of implantable ( Class III) Cardiac and Neuromodulation medical device related products. Initial scope of work may be focused on Inspec...
Summary : The Supplier Quality engineer will work closely with our suppliers and purchasing group to resolve supplier issues and prevent their reoccurrence. Applies and maintains standards for manufacturing, quality, design, testing, and i...
activities, including packaging integrity, shelf life, and transit testing. * Hands-on experience in Process validation (IQ, OQ...
-disciple engineers and design leads that form the core of our Life Safety Systems delivery team. Utilizing AutoCAD and Revit..., Access Control and CCTV. Preferred Qualifications: 3-5 years of life safety systems design experience. Knowledge of IFC...