Quality System Engineer Ii

EDUCATION and/or EXPERIENCE Bachelor's degree in engineering (industrial, chemical, manufacturing, or any other related). And/or 3 years on QA/QC engineering work experience on QA/QC in medical device manufacturing processes such device assembly, injection molding or extrusion, preferable. Preferable ISO 13485 certified internal auditor. CPF-815...

Descripción y detalle de las actividades Supports Quality System compliance by managing the Internal Audit process and CAPA system. ESSENTIAL DUTIES AND RESPONSIBILITIES: -Implements and supports methodologies and systems that improve product quality and QS (Management Review, QSR Training, ISO13485). -Assist organizational and group operations management...

**Eaton’s Aerospace ITD division is currently seeking a Sr. Quality System Engineer to join our team.** This position is based at our Tijuana facility. The Sr. Quality System Engineer is responsible for drives the development and implementation of the Eaton Quality Management System, Quality Best Practices & Eaton Quality Lead Indicators. Ensures that...

Descripción y detalle de las actividades Responsibilities: - Implements policies and procedures to enhance the Quality System, advises on methodologies regulating product quality: ISO 13485:2016, MDD and CMDCAS, MDSAP, CFR21 Parts 820 and 11. - Coordinates and manages activities related to Corrective and Preventive Actions, Internal Audits. - Plans,...

At Medtronic, you'll have the opportunity to drive quality and innovation in our supply chain. As a Supplier Quality Engineer II, your primary focus will be ensuring that suppliers deliver high-quality parts, materials, and services.Key Responsibilities:Evaluate and qualify suppliers based on company standards and may administer a certified supplier program...

Descripción y detalle de las actividades Quality Engineer I is responsible for ensuring the safety and quality of our products and procedures through rigorous inspections, implementation of quality control measures, and identification of areas for improvement, collaborates with cross-functional teams to address quality issues, drive continuous improvement,...

Descripción y detalle de las actividades - Manage all quality-related issues within the manufacturing team (e.g. internal, supplier, customer, and customer warranty) - Identify root cause and instigate permanent corrective actions for product quality issues. - Carry out product and process auditing. - Ensure control plans and associated documentation are...

Eaton’s IS VEH EMB division is currently seeking a Quality Engineer. **What you’ll do**: **Primary Function**: Responsible to validate and verifying manufacturing systems; including process documentation, controls and optimization through the life of the product to ensure internal quality, customer satisfaction and drive automotive culture. Quality...

Eaton’s VEH EMB eMobility division is currently seeking a Quality Engineer. **What you’ll do**: **Main goal** Responsible to validate and verifying manufacturing systems; including process documentation, controls and optimization through the life of the product to ensure internal quality, customer satisfaction and drive automotive culture. Quality...

Descripción y detalle de las actividades Duties include execution of all quality-related activities. This includes but is not limited to Quality System; Quality Engineering functions; Inspection activities, Gage Calibration and Document Control. Responsible for all Documentation Control activities associated with Quality System requirements, including...

Descripción y detalle de las actividades Lead and drive document control area (Deviation, Procedures, Work Instructions and forms on the site) Lead internal and external audits or customer quality related audits Be main contact with external auditor for quality certificates with DQS and Nadcap Be main contact with customer audits ans BEI corporate quality...

Descripción y detalle de las actividades Be a part of a team of Quality Engineers that applies its expertise and knowledge in finding innovative, cost-effective means to improve quality output and continuous improvements. Key Responsibilities: - Internal auditing of Lab Quality System processes and procedures. - Perform daily verification of the...

Descripción y detalle de las actividades What you will do As the Computer System Validation (CSV) Engineer you will: - Develop Computer Systems validation test strategy, test plans, test automation scripts, and test procedures to meet requirements. - Develops, and executes/coordinates protocols and test scrip, identify gaps, consult on and direct plans for...

Descripción y detalle de las actividades Job Purpose Summary Responsible for developing strategies and initiatives for maintaining the CAPA and Audit Quality Programs aligned with medical devices Regulations, Standards Requirements and Company goals and objectives. Primary responsibility is to maintain the activities related to CAPA and Audit Quality...

Descripción y detalle de las actividades - Lead and drive Quality improvement on CFT. -Support for FAI reports from new products of transferences. -Support Customer complaints. -Be main contact of customers for quality topics related. -Approve documentation in PFS, Agile. -Material management in LN system. -Generate WI as necessary in Agile...

In our ‘always on’ world, we believe it’s essential to have a genuine connection with the work you do. Manufacturing Engineer II In our ‘always on’ world, we believe it’s crucial to have a genuine connection with the work you do. Technology is reshaping the way we live, learn and thrive. In this "always-on" world, we believe it is relevant to...

**Why engineering at Stryker?****: At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other...

About the RoleWe are seeking an experienced Quality Engineer II to join our team at Carlisle Interconnect Technologies. The ideal candidate will have a strong background in engineering or quality assurance, with excellent analytical and problem-solving skills.

Descripción y detalle de las actividades Duties include execution of all Incoming quality-related activities. This includes but is not limited to Quality System; Quality Engineering functions; Inspection activities, Gage Calibration and Document Control. Responsible for all Documentation Control activities associated with Quality System requirements,...

**Descripción y detalle de las actividades** - Key responsibilities: -Define and oversee effective implementation of the Quality Management System.Define and maintain the Quality Manuals and Procedures and ensure contents are appropriate for the company.Perform gap analysis to detect opportunities areas to improve internal and external quality/manufacturing...