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Commissioning Qualification and Validation (CQV) Engineer

Altran AG

 
Zürich, Switzerland
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Altran ranks as the undisputed global leader in Engineering and R&D services (ER&D). The company offers clients an unmatched value proposition to address their transformation and innovation needs. Altran works alongside its clients, from initial concept through industrialization, to invent the products and services of tomorrow. For over 35 years, the company has provided expertise in Automotive, Aeronautics, Space, Defense & Naval, Rail, Infrastructure & Transportation, Energy, Industrial & Consumer, Life Sciences, Communications, Semiconductor & Electronics, Software & Internet and Finance & Public Sector.

Now part of Capgemini, Altran Group is the global digital transformation leader for industrial and tech companies with 250’000 consultants worldwide.

Follow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as,

Commissioning Qualification and Validation (CQV) Engineer

Our offer

  • A permanent contract with the leader in innovation and high-tech engineering consulting
  • A multi-stage model with career opportunities through specialization prospects with over 250'000 consultants around the world and a Group revenue (Altran/Capgemini) of EUR. 17 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D)
  • In Switzerland, Altran employs more than 400 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.

Responsibilities:

  • Support of continuous improvement on process, and on Qualification and Validation projects.
  • Generate and execute CQV protocols using Good Documentation Practices (GDPs).
  • Investigate and resolve protocol exceptions or discrepancies.
  • Develop technical reports and CQV summary reports.
  • Collaboration in the creation of user requirements (URS).
  • Create / check DQ, IQ, OQ and PQ documents.
  • Participation in GMP relevance and risk analyses.
  • Develop Standard Operating Procedures (SOPs), process workflows, Validation Master Plans, User Requirement Specifications, Turnover Packages, and other regulatory support documentation (CAPA etc).

Your profile:

  • BSc/MSc degree in Engineering or Chemistry or any related field.
  • Minimum 3 years of experience in Commissioning and/or Qualification and/or Validation in the Pharmaceutical industry.
  • Applied knowledge of international Pharmaceutical regulations is preferred.
  • Applied Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ).
  • Fluent in English and German.

If your profile matches the requirements of the position, we will contact you within the next fifteen (15) days of submitting your application. Otherwise, please kindly consider that your application is unsuccessful.

Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.

Altran is an EEO and Affirmative Action Employer of Females/Minorities/Individuals with Disabilities.

Adresse

Altran AG
Ms Yudishni Mahadeo

Site web http://www.altran.ch

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