62820 Jobs Found for Iq Resource Group
The Validation Engineer will be responsible to ensure that validation requirements are met for all existing and new equipment/ facilities/utilities and processes by preparing and executing detailed validation protocols that meet the relevant testing standards and any requirements. Responsibilities: Designs and drafts validation sampling and testing...
Roles and Responsibilities: Drive projects with suppliers to continuously improve business and manufacturing process performance, aligning with standards for supplier excellence. Identify and select processes and suppliers that align with long-term fit and total cost of ownership considerations. Lead project and part qualification activities incl...
Responsibilities: Establish and maintain design history file documentation for development projects (design and development plan, requirements specifications, device master record, IOV matrix, verification, validation summary reports, etc.) Establish and maintain risk management documentation (risk management plan, hazards analyses, failure mode, a...
Job Description Primary Function of Position As a member of the manufacturing engineering team, you will work in a dynamic, fast paced, and challenging environment. You will be responsible for supporting production of Da Vinci Surgical Robotic systems by applying your knowledge of system engineering including software, and electromechanical assemb...
Top Skills: • Bachelor’s degree (B.S.) in related field or equivalent. • Five year’s related experience or equivalent in a Medical Device or FDA Regulated industry. • Knowledge of fundamental cGMP concepts and FDA/EMA regulations, QSR, 21 CFR Part 820, 21 CFR Part 11, ISO 13485:2003 and ISO 9001 Standards • Strong knowledge of FDA Regulated manufac...
Key Responsibilities: Validation Protocols: Develop and execute validation protocols (IQ, OQ, PQ) for manufacturing equipment, processes, and software systems to ensure compliance with FDA and ISO regulations. Documentation: Prepare and review validation documentation, including validation plans, test protocols, and final reports, ensuring accur...
Top Skills: • Bachelor’s degree (B.S.) in related field or equivalent. • Five year’s related experience or equivalent in a Medical Device or FDA Regulated industry. • Knowledge of fundamental cGMP concepts and FDA/EMA regulations, QSR, 21 CFR Part 820, 21 CFR Part 11, ISO 13485:2003 and ISO 9001 Standards • Strong knowledge of FDA Regulated manufac...
Medical Device Process Engineer 9 month+ possible temp to direct Work on-site in Santa Clara Develop and execute process validation protocols (IQ, OQ, PQ) in accordance with FDA and ISO regulations Familiar with medical device manufacturing processes; UV curing, catheter shaft fabrication (braiding and plastic re-flow), fusing, tipping, sol...
A leading contract manufacturer for Medical Devices is in immediate need of a Sr. Automation Engineer for a 3-6 month project that will be based fully onsite in either Scottsdale or Phoenix. Top Requirements : BS degree minimum in Engineering. Experience managing multiple capital equipment projects within FDA-regulated industry. Subject Matter Ex...
The Validation Engineer will be responsible to ensure that validation requirements are met for all existing and new equipment/ facilities/utilities and processes by preparing and executing detailed validation protocols that meet the relevant testing standards and any requirements. Responsibilities: ? Designs and drafts validation sampling and testi...