Validation Engineer Ii

BEPC has a Tijuana area OPEN POSITION for **Validation Engineer I - II **to join our fast-growing team of consultants! This role will be working on the shop floor to define the impact of the variant part and components, directly working with associates, group leaders and supervisors. Responsible for Assessments, Process validations, Software validations,...

1 to 3 years experience in Medical devices as engineer. Validation protocols execution experience IQ, OQ, PQ. Knowledge in statistics Write/Execute Change Management/Change Control Assessments (e. g. Validation, Process etc.). Create/Execute Engineering Changes Orders. Write/Approve changes related to manufacturing documentation such as Manufacturing Work...

This role is responsible will be working on the shop floor to define the impact of the variant part and components, directly working with associates, group leaders and supervisors.KEY RESPONSIBILITIES: Ability to manage projects, lead teams in different places performing projects. Write/Execute Process Validation Protocols (IQ, Create/Execute Engineering...

**Company Overview** Outset is a medical technology company pioneering a first-of-its-kind technology to reduce the cost and complexity of dialysis. The Tablo Hemodialysis System, FDA cleared for use from the hospital to the home, represents a significant technological advancement that transforms the dialysis experience for patients and operationally...

Company OverviewOutset is a medical technology company pioneering a first-of-its-kind technology to reduce the cost and complexity of dialysis. The Tablo Hemodialysis System, FDA cleared for use from the hospital to the home, represents a significant technological advancement that transforms the dialysis experience for patients and operationally simplifies...

Job TitleValidation Engineer - LED ElectronicsJob Description:We're looking for a strong Validation Engineer to join our LED Electronics R&D team in Tijuana, Mexico.Working for Signify means being creative and adaptive. Our culture of continuous learning and commitment to diversity and inclusion creates an environment that allows you to build your skills and...

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...

Our client is a German global leading Medical devices manufacturer and they are looking for aSoftware Validation Engineer for their manufacturing facility in Tijuana, B.C. Design and develop test plans, procedures and generate test reports. Develop and execute automation scripts. Assist developers in debugging customer issues. Maintain/update defects...

1 to 3 years experience in Medical devices as engineer. - Validation protocols execution experience IQ, OQ, PQ. - Knowledge in statistics - Write/Execute Change Management/Change Control Assessments (e. g. Validation, Process etc.). Create/Execute Engineering Changes Orders. Write/Approve changes related to manufacturing documentation such as Manufacturing...

Job Description 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...

EDUCATION and/or EXPERIENCEBachelor'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 /23)Knowledge by...

Job Description 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....

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...

Our client is a German global leading Medical devices manufacturer and they are looking for a **Software Validation Engineer** for their manufacturing facility in Tijuana, B.C. - Design and develop test plans, procedures and generate test reports. - Develop and execute automation scripts. - Assist developers in debugging customer issues. - Maintain/update...

Job Title Validation Engineer - LED Electronics **Job Description**: We’re looking for a strong Validation Engineer to join our LED Electronics R&D team in Tijuana, Mexico. Working for Signify means being creative and adaptive. Our culture of continuous learning and commitment to diversity and inclusion creates an environment that allows you to build...

This role is responsible will be working on the shop floor to define the impact of the variant part and components, directly working with associates, group leaders and supervisors. **KEY RESPONSIBILITIES**: - Write/Execute Process Validation Protocols (IQ, Create/Execute Engineering Changes Orders - Write/Approve changes related to manufacturing...

**Position** **Sector / Department** Process Engineer II Engineering **Job Position Accountabilities / Expectations** 1. Coordinates & Executes complex projects based on specialized knowledge. 2. Designs, proposes, and/or implements new systems, that require knowledge on different continuous improvements techniques. 3. Lead or participate in cross...

PositionSector / DepartmentProcess Engineer IIEngineeringJob Position Accountabilities / ExpectationsCoordinates & Executes complex projects based on specialized knowledge.Designs, proposes, and/or implements new systems, that require knowledge on different continuous improvements techniques.Lead or participate in cross functional project teams for...

y detalle de las actividadesAccountable for existing processes sustaining for the applicable areas. Also, is responsible of development and continuous improvement of manufacturing processes. May have complete project responsibility for significant projects within specialized area and participate in the activity's execution of the VIP's Projects.Key...

Job DescriptionRESPONSIBILITIES Design and develop test plans, procedures and generate test reports. Develop and execute automation scripts. Assist developers in debugging customer issues. Maintain/update defects database with a defect tracking system. Support determining root cause of defects through structured analysis Manage validation schedules based on...