Quality Engineer

We are seeking a Supplier Quality Engineer to join our dynamic team of industry leading experts. Under the direction of the Quality Manager, in this position, you will drive the Implementation and monitor the corporate quality requirements for the company suppliers, perform product and process issue resolution and manage process control and...

**Location**: Cartago, Costa Rica, CR **Job Family**: Quality Assurance **Country/Region**: Costa Rica Quality Systems Engineer Quality System Engineer, Coloplast Cartago Are you motivated by quality control of medical device products with the purpose of improving the lives of people with intimate health care needs? We are looking for a dedicated...

**Summary**: The Quality Assurance Associate receives training on the Baylis Quality Management System. They perform investigations and analyses within a well-defined scope and objectives. They may provide quality process guidance in areas which they are assigned to others in the organization. Key Responsibilities: Collect, organize and synthesize to support...

**Key Responsibilities**: - Write, review and/or approve validation protocols and reports (e.g., cleanroom, equipment, test method and product transfer validation protocols) in accordance with applicable Regulations, Edwards Lifesciences SOPs and Good Documentation Practices (GDP) Utilize test equipment to verify equipment parameters, process outputs or...

**Engineer II, Quality temporary position 12 months**: - Remote Eligible: Onsite- Onsite Location(s): Cartago, CR**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of...

**Location**: Cartago, Costa Rica, CR **Job Family**: Quality Assurance **Country/Region**: Costa Rica Job function summary The Quality Engineer ensures compliance to external and internal quality requirements and provides support to Operations value stream in accordance with Coloplast Quality Management System. Major areas of accountability - Create...

Ensure compliance of the QMS and compliance within quality processes (e.g., CAPA. NCR, ECR, internal and external auditing, training). Maintain quality reporting inclusive quality and production indicators. **Key Responsibilities**: - Provide complex assessments including audits to ensure conformance with applicable regulations and EW policies and...

Supervises employees responsible for Quality Inspection. **Key Responsibilities**: - Supervise employees and quality activities pertaining to the production of products and/or manufacturing processes in - and with quality/technical knowledge of 2 or more production areas, depending on the complexity of the areas, in addition to conducting performance...

**Equipment Engineer I**: - Remote Eligible: Hybrid- Onsite Location(s): Cartago, CR**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing...

**SUMMARY** A process development engineer plans, designs and executes cost-effective production systems, in order to enhance the speed and quality of processing, and ensure produced items comply with international regulations and industry standards. Process development engineers use technical knowledge and industry expertise to review existing...

Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. **Key Responsibilities**: - Investigate moderately complex manufacturing product quality and compliance issues...

Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. **Key Responsibilities**: - Investigate basic manufacturing product quality and compliance issues (e.g., CAPA,...

Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Key Responsibilities: - Investigate moderately complex manufacturing product quality and compliance issues...

**Ubicación**: Cartago, Costa Rica, CR **Familia de puestos**: Control de Calidad **País**: Costa Rica Job function summary The Validation Engineer will be responsible for the execution of process and software validation activities under the organizations as well as maintaining the validation life cycle of the machines, process, and test method, ensure...

**Engineer II, Equipment**: - Remote Eligible: Hybrid- Onsite Location(s): Cartago, CR**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing...

**Key Responsibilities**: - Write, review and/or approve validation protocols and reports (e.g., cleanroom, equipment, test method and product transfer validation protocols) in accordance with applicable Regulations, Edwards Lifesciences SOPs and Good Documentation Practices (GDP) Utilize test equipment to verify equipment parameters, process outputs or...

**SUMMARY**: The Validation Engineer will be responsible for performing and overseeing the validation of manufacturing processes. Support the quality assurance of all activities within the process, ensuring that all systems are running according to the specifications and operations standards monitoring budget, and controlling purchase and...

Requisitos: BS in engineering/Electrical Engineering or Mechanical Engineering At least 3-year experiences in Manufacturing Quality Assurance in a manufacturing environment Proven knowledge in quality tools, packaging supplies, electronic components and plastic components. Proven knowledge in electrical components failure analysis ISO 9001 internal...

**Location**: Cartago, Costa Rica, CR **Job Family**: Quality Assurance **Country/Region**: Costa Rica Job function summary The Validation Engineer will be responsible for the execution of process and software validation activities under the organizations as well as maintaining the validation life cycle of the machines, process, and test method, ensure...

**Intern Training Engineer (Cartago)**: - Remote Eligible: Hybrid- Onsite Location(s): Cartago, CR**Additional Locations**: N/A **Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - Caring - High Performance** At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and...