Validation Expert in Zug

veröffentlicht
Kontakt
Mayank Chaubey, Basel Professionals IT & Life Sciences
Jobtyp
contract
Jetzt bewerben

job details

veröffentlicht
Ort
Zug
Sektor
Life Sciences
Jobtyp
contract
Referenznummer
9788
Kontakt
Mayank Chaubey, Basel Professionals IT & Life Sciences
Telefon
058 201 55 50
Jetzt bewerben

Stellenbeschreibung

Our client, a leading international pharmaceutical company, based in Rotkreuz is currently looking for

Validation Expert 


Location: Zug, Switzerland
Contract: 01.011.2017 – 31.12.2018 (possibility of extension)


Main duties


Independent implementation and documentation of validation and verification. Qualification activities according to valid specifications and project planning, in close
cooperation with internal and external partners / interfaces of operations. Instrumentation, in particular for instrumentation and all custom made systems of the department tech support. Jointly responsible for ensuring compliance in accordance with the applicable internal prescription documents. Review of validation / Qualification documents, and formal examination.

Essentially the role requires following criteria:

  • Planning and carrying out validation and qualification tasks, and maintenance of existing qualification documentation.
  • Qualification of equipment, e.g. Standard equipment, custom built systems or measuring instruments.
  • Validation of software and Excel workbooks, according to CSV (Computerized system validation).
  • Validation of test sites (custom built, consisting of several subsystems including software components).
  • Participation in the internal process validation of the device production and the implementation of method validations.
  • Creation of validation / qualification plans and reports, as well as test plans / reports.
  • Support and professional advice to operators and users of equipment / systems for the execution of validation and training tasks.
  • Reporting, coordination and coordination of the priorities with the clients, partners / interfaces, e.g. Sub project leader, product leader, line manager and contact persons from the departments.
  • Collaboration in the preparation of risk analyzes of equipment / systems

Professional experience

  • Hochschul- oder Fachhochschulabschluss

Required Experiences:

  • Experience in the regulated GxP environment is usually based on medical technology (ISO 13458, GMP, FDA 21 CFR 820).
  • You have a marked quality consciousness and a structured, scientific approach.
  • Profound computer skills (SAP, MS Office) as well as understanding of complex hard-Software architectures are an advantage.
  • You value independent and responsible work in a versatile product and project environment.
  • You are also characterised by high performance.
  • Teamwork, flexibility and resilience, and other appropriate qualifications bring you a challenging task in our complex process landscape with plenty of variety to succeed successfully.

Languages 

  • German- Fluent
  • Englisch - Advanced

Knowledge of IT systems

  • Microsoft Office, SAP and Google - Production system: VBA, Access, Labview, Delphi und SQL

If this interest then we are looking forward to receiving within your application, Please provide:

  • your CV in German
  • latest Work Certificates
  • your Motivation Letter in German
  • the date of your availability

Apply now to be considered – Good to know you!


For more information and your application, please contact:


Mayank Chaubey, PhD

Consultant Professionals Life Sciences
Randstad (Suisse) SA

T +41 58 201 55 62 M +41 79 513 24 83

mayank.chaubey@ch.randstad.com