Process/Validation Engineer (m/w)

  • Type de contrat Poste fixe - 1 an
  • Lieu
    Tolochenaz
  • Référence 206958-32-10
  • Date d'entrée asap
  • Secteur Technique & Ingénierie
  • Date de publication 04.05.2021
  • Postuler

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

Process/Validation Engineer (m/w)

Votre mission

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 projects

As 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

Votre profil

* 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 French
Competencies
* 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

Vous reconnaissez-vous ?

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

A propos de Manpower
En Suisse, Manpower est fort d’une expérience de plus de cinquante-cinq ans dans le recrutement, la sélection et le placement de personnel fixe et temporaire, ainsi que dans les solutions RH. Avec 50 agences présentes dans toutes les régions linguistiques, 20 000 collaborateurs temporaires, 1500 placements fixes et plus de 5000 clients – petites, moyennes et grandes entreprises – actifs dans tous les secteurs d’activité, Manpower est l’un des leaders du placement de personnel en Suisse.
 
Nos 3 promesses
« Nous aimons ce que nous faisons. Cette passion qui nous porte et nous motive vous donne les meilleures chances de placement. »
« Nous apprécions les gens avec qui nous travaillons. Vous, par exemple. C’est pourquoi nous fondons notre collaboration sur la confiance. »
« Nous assumons nos responsabilités. Pour vous, cela signifie sécurité et perspectives intéressantes. »
 
 

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Votre conseiller Manpower
Mathilde Augusto

Life Sciences Competence Center
Picassoplatz 4
4052 Bâle

T: +41 58 307 2441



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