Process/Validation Engineer (m/w)

 — Tolochenaz
04 May | Executive po­si­tion | 100%

Introduction :

Référence filiales : 156-MORGES

Nom du conseiller : Augusto Mathilde

Nom de la filiale : 11

Adresse :

19, Grand-Rue



Description de l'entreprise :

For one of our clients, leader in the Medical Device industry, we are currently looking for a

Secteur d'activité : Technique & Ingénierie

Process/Validation Engineer (m/w)


Your mission: accelerate new products launches by implementing innovative and cost-effective manufacturing process solutions and by:• Qualifying/validating manufacturing processes/products• Understanding product requirements and their design intent, and providing constructive design feedback through fast prototyping and engineering builds• Driving standardization and setting high-quality standards to reach yields and process capabilities• Participating in product development projectsAs a Process Engineer, you will:• Conduct OQ/PQ for new product/process according to schedule until pass-off requirements are met (incl. knowledge transfer)• Participate in local/global projects• Evaluate, characterize, qualify and validate product/process/line in the assigned scope of processes• Increase process capability (CpK)• Support product development activities• Participate in Design comprehensive engineering activities to develop and implement effective, high-quality processes and design guidelines.• Provide complex design reviews and feedback for improvements in manufacturability.• Help to establish and maintain the required documentation (e.g. OQ/PQ plan & report)• Follow the established quality standards• Improve product quality by applying design for reliability and manufacturability practices• Communicate with internal/external stakeholders• Be pro-active to answer customer needs

Date d'entrée : 06-05-2021

Type de société : Entreprise privée

Reference : 206958-32-10

Date de publication : 2021-05-04 17:13:12

Profil recherché :

* Engineering Degree (HES/EPF or equivalent) in Chemicals, Materials, Mechanics, Physics or Microengineering• Experience in Medical Devices and/or Pharma industries• Exposure to Compliance/Quality Systems Regulations (e.g. GMP's, process/document controls, CAPA, audits)• Fluent in English and FrenchCompetencies• Knowledge in manufacturing processes validation (OQ/PQ)• Good analytical skills (e.g. applied to risk analysis, problem-solving, to find creative/innovative solutions)• Proactive, flexible, results-oriented, and motivated by achievement• Good communication skills• Autonomous, team player, contribute to others' success beyond own expertise and organization• Excellent Microsoft Office practice and knowledge• Knowledge and practice of Lean Manufacturing (e.g. continuous improvement mindset, process excellence) is a nice to have• Knowledge in Data analysis and Statistics (Cpk, Ppk, Confidence Interval, ANOVA, "¦) is nice to have

Pays : Suisse

Lieu de travail : Tolochenaz

Code postal : 1131

Catégorie : Contrôle Qualité / Process;Electronique / Electrotechnique;Ingénieur / R & D

Niveau d'études : Expérience professionnelle : Début du contrat : 06.05.2021Durée du contrat : Non précisé

Conclusion :

Have we picked your interest? Do not hesitate to apply directly!

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