Service:

Ambu

Publiée le
10/06/2026
Contrat
Freelance · Inconnue
Localisation
, , ,
Taille équipe
Inconnue emp.
Rémunération
Inconnue
Inconnue Inconnue ans exp. Italien

Avantages

Open spaceSemaine de 4 jours
Missions clés Validate automation systems and/ process improvements (IQ/OQ/PQ) and support the development of automated solutions · Promouvoir culture of innovation
Profil recherché Bac +8 (Doctorat) · Rigueur · Esprit d'analyse
Outils & compétences Selenium, Python

Le poste en détail

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Modify Cookie Preferences Reject All Cookies Accept All Cookies About us Jobs Our People Hiring process Values Language View profile Job Description Job Alerts Link Apply now open/close Print local Share on Twitter Share on LinkedIn Send as email Process Validation Engineer, Advanced Manufacturing Engineering City: Noblesville Country/Region: United States State: Indiana Business Area: Production Department: Production, NV - IE Employment Type: Full-time Req ID: 9766 Ambu provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This role will be based out of the Ambu America's Center of Excellence located at the Noblesville, Indiana manufacturing facility. The role has overall responsibility for the Advanced Manufacturing Engineering functions of both the Noblesville, IN and the Juarez, MX manufacturing sites. The expected travel for this role is up to 50%. Objective: The Process Validation Engineer leads the validation aspects of Automation and Equipment Capital projects, process improvements, supports the development of automated solutions, is responsible of the validation of new equipment installation, ensuring seamless process transfer and readiness to production. Responsibilities and Essential Functions: Compliance and Validation: Validation Documents preparation and execution, to ensure all automated systems and/or process improvements are validated (IQ/OQ/PQ) and fully compliant with 21 CFR Part 820 and other applicable standards, before release to production. Evaluation of validation strategy to ensure quick and compliant transfer of processes and equipment to production. Maintenance of the Agile documents related to processes and equipment, like SOP, flow charts, electrical drawings, 2D/3D drawings, equipment parameter list (CP), equipment logic program (LCP). Complying with FDA QSR, ISO 13485, and relevant product-specific regulations (e.g., IEC 60601, ISO 14971). Operational & Regulatory Excellence Automation & Smart Manufacturing: Assist to the design and implementation of automated manufacturing and assembly systems (e.g., robotics, PLCs, vision systems, motion control) to support precision, repeatability, and compliance. Assist to automation and equipment capital projects from concept to installation and validation. The role requires to be “hands on”, on the process and equipment, when needed. Operational Excellence: Champion Lean, Six Sigma, and Design for Manufacturability (DFM/DFA) principles across internal and outsourced operations. Authorities: Ability to approve validation protocols, test plans, and reports. Authority to sign off on equipment and process validation documentation. Determine corrective and preventive actions (CAPA) related to validation findings. Work Environment: This is a manufacturing facility and as a result, employees have the potential to be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration or other workplace hazards controlled within compliance of current safety and health standards. Qualifications: Bachelor’s degree in related field and 3 - 5 years of relevant work experience. Five years’ experience working in the medical device field. Strong background in medical device process validation, and regulatory compliance. Ability to complete complex reports and correspondence. Must be able to speak, read, write and understand English. Bilingual in Spanish is preferred. Ambu Provided Training within the first six months: Agile, Change Control System Movex, ERP System Medius, Procurement System Validation Training About Ambu Ambu has been bringing the solutions of the future to life since 1937. Today, millions of patients and healthcare professionals worldwide depend on the efficiency, safety and performance of our single-use endoscopy, anesthesia, and patient monitoring solutions. We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of healthcare professionals. Headquartered near Copenhagen in Denmark, Ambu employs approximately 4,500 people in Europe, North America and the Asia Pacific. For more information, please visit ambu.com or follow us on LinkedIn. About Ambu Ambu has been bringing the solutions of the future to life since 1937. Today, millions of patients and healthcare professionals worldwide depend on the efficiency, safety and performance of our single-use endoscopy, anaesthesia, and patient monitoring solutions. We continuously look to the future with a commitment to deliver innovative quality products that have a positive impact on patient care and the work of healthcare professionals. Headquartered near Copenhagen in Denmark, Ambu employs approximately 4,500 people in Europe, North America and the Asia Pacific. For more information, please visit ambu.com or follow us on LinkedIn. Apply now SHORTCUTS See all products See all clinical evidence Find distributors Ambu addresses Contact us Research Support SHORTCUTS Financial News Job openings SOCIAL MEDIA Opens In A New Tab. Opens In A New Tab. Opens In A New Tab.