Quality / Validation Engineer (w/m/d)

Solothurn - Schweiz - Life Sciences & Gesundheitswesen - Biotechnik - Gesetzgebung - Master of Science/ Engineering/ Arts oder Diplom Fachhochschule

Do you want to take the next step up in your career? Brunel gives you the chance to continually develop and improve with big-name clients across a broad variety of industries. Take that crucial career step today: Apply to join Brunel as a Quality / Validation Engineer.

Wir stehen für Rückfragen zur Verfügung

Jassin Stocker, Ansprechpartner

Bewerben

Ihre Aufgabe

  • Preparation and execution of validation protocols involving facilitates equipment, utilities and associated automation
  • Preparation, review and approval, Validation Master Plan and SOPs
  • Coordination and management of validation activities
  • Deliver cross functional training in validation methodologies
  • Point of contact for validation related issues
  • Ensure site Validation Program meets company global directive
  • Investigation of deviations and non-conformances, to determine the impact on product quality, validation status and associated compliance requirements
  • Review and approve Change Management applicable to any system
  • Perform risk and impact assessments associated with validation activities
  • Provides support to commissioning activities, including review of commissioning plans and procedures
  • Review established Engineering Guidelines and Specifications
  • Performs final review and provide final reports to ensure conformance with the company established specifications
  • Provide guidance on validation requirements and expectations to validation engineers
  • Represent the validation program and designated validation activities during inspections

Ihr Profil

  • Bachelor of Science, Degree (BSc) in an engineering or scientific discipline
  • Master in a related discipline preferred
  • 10-15 years’ experience in a Validation/Quality role
  • Excellent knowledge of Good Practice requirements (GMP, GEP) as well as biopharmaceutical industry regulations and norms as they relate to validation
  • Previous experience in a manufacturing, biopharmaceutical environment
  • Large scale project experience
  • Strong technical writing and communication skills
  • Proficiency in MS Word, MS Excel and MS Project.
  • Ability to take pragmatic and compliant decisions.
  • Highly motivated to take project ownership
  • Ability to take the initiative with minimal supervision
  • Fluent in English

Wir bieten

From medium-sized companies to hidden champions and large conglomerates; whether road, ship, rail, air or space; traditional or innovative; from development to finished product; national or international; from a career starter to an experienced professional. We offer you countless opportunities to help shape technological progress, and all of this with just one employer.

Über Brunel

To work for Brunel is to experience attractive work assignments, look forward to positive career prospects, enjoy the secure backing of a growing employer and explore the sheer diversity of the world of engineering. We have more than 40 offices and 3 development centers in German-speaking Europe, and our 97 offices worldwide employ more than 10,000 people. To stand still is to fall behind, so stay on the move with Brunel.

Zusammenfassung

  • Kennziffer des Stellenangebots: PUB199140
  • Ort: Solothurn
  • Markt: Life Sciences & Gesundheitswesen
  • Stunden pro Woche: 42
  • Branche: Biotechnik
  • Ausbildungsgrad: Master of Science/ Engineering/ Arts oder Diplom Fachhochschule
  • Fachgebiet: Gesetzgebung
  • Einsendeschluss: Samstag, 30. März 2019
Bewerben

Wir stehen für Rückfragen zur Verfügung

JS

Jassin Stocker

Ansprechpartner Brunel Switzerland Zürich

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