Process Validation Engineer

Merck KGaA Darmstadt Germany

Visualizza: 200

Giorno di aggiornamento: 20-03-2024

Località: Aubonne Vaud VD

Categoria: IT - Software

Industria:

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Contenuto del lavoro

Une carrière chez nous, c’est un parcours continu de découvertes : nos quelque 58 000 collaborateurs façonnent la manière dont le monde vit, travaille et se divertit à travers des avancées de nouvelle génération dans les domaines Healthcare, Life Science et Electronics. Depuis plus de 350 ans et dans le monde entier, nous exploitons sans relâche notre curiosité afin d’identifier des méthodes inédites et dynamiques visant à améliorer la vie d’autrui.

Tous unis pour les patients : l’objectif de la branche Santé est de contribuer à créer, améliorer et prolonger des vies. Nous développons des médicaments, des dispositifs intelligents et des technologies innovantes dans les domaines thérapeutiques tels que l’oncologie, la neurologie et la fertilité. Nos équipes travaillent sur les 6 continents avec passion et curiosité dans le but d’aider les patients à tous les stades de leur vie. Rejoindre notre équipe Santé signifie participer à une culture professionnelle diversifiée, ouverte et flexible offrant de belles opportunités pour le développement personnel et l’évolution de carrière à travers la planète.

An exciting new opportunity has arisen to join our company as Project & Process Engineer in our Packaging Science And Technology team which is part of Supply Operations department in Aubonne.

New Packaging Development, Innovation, New Business Entity, Product Lifecycle Management & Artworks implementation are the driving forces of this future oriented team.

Your role:

As project lead or stakeholder, your main fields of action are:
  • Managing activities for new product introduction for Aubonne’s site
  • Managing lifecycle projects to ensure the continuity of commercial products supply.
  • CAPEX projects participation in collaboration with local Engineering

This job will require the realization of activities such as (non-exhaustive list):
  • Writing of URS, Validation Plans, Protocols, Reports
  • Creation of Change Controls
  • Establishment of projects GANTT chart
  • Organization and execution of process and shipping validations
  • Lead/participation in risk analysis (process, equipment, CCP)

In this position, you will be involved in internal collaborations with supply operation units (packaging, logistic, planning), other departments (e.g. FDF, Technical Services), Quality Unit & Regulatory.
This role also offers you the opportunity to collaborate with external partners as suppliers, subcontractors, global functions (CHD, SNO, GRA, MLT leaders) and other Merck’s sites.

Who you are:
  • Minimum Bachelor’s degree in engineering or medically related fields
  • Experience in international pharmaceutical companies
  • Experience in validation is a plus
  • Good knowledge of pharmaceutical business, Good Manufacturing practices (GMP) and Health Authorities requirements
  • Good knowledge of packaging processes
  • Strong leadership and influencing skills
  • Strong interpersonal skills and ability to interact positively and constructively with all functions
  • Good project management skills
  • Experience in medical devices is a plus
  • Fluent in French and in English (written and spoken)


Ce que nous vous offrons :Chez nous, les opportunités d’innovation sont permanentes. Nous vous offrons l’opportunité de réaliser vos ambitions et nos différentes activités offrent plusieurs possibilités d’évolution de carrière à ceux qui sont à la recherche de nouveaux horizons. Nos collaborateurs se voient confier des responsabilités de façon précoce et nous vous offrons le soutien nécessaire pour élaborer votre propre plan de carrière, en accord avec vos aspirations et vos priorités dans la vie. Rejoignez-nous et exploitez votre curiosité !

Envie d’en savoir plus ? Envoyez-nous votre candidature et recherchez d’autres informations sur https://jobs.vibrantm.com

Numéro de demande de recrutement: 224453

Lieux: Aubonne

Expérience Professionnelle: D - Professional (4-9 years)

Modèle de temps de travail: Temps plein

US Disclosure
The Company is an Equal Employment Opportunity employer. No employee or applicant for tunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday.

Segment de l’offre d’emploi:Developer, Neurology, Oncology, Medical, Pharmaceutical, Technology, Healthcare, Science

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Scadenza: 04-05-2024

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