Aristo Group

Quality Multi Discipline Contractor (m/w/d)

Mehr als 30 Tage alt

Angaben zum Job

Aristo Group
Firma Aristo Group Personalvermittler
Pensum 100%
Einsatzort Bern

Job-Inhalt

Industry: Pharma
Skills: GMP,CVQ,QA

Start of project: 10.12.2024

Duration of the project : 7 Monate

Project volume: 42 Stunde(n) 

Location: Bern, Schweiz

Tasks:

  • Ensure compliance with quality standards during commissioning and qualification activities (DQ, IQ, OQ, PQ).
  • Review and approve system-specific documentation such as URS, RTM, QRA, and IOC related to C&Q processes.
  • Develop and implement guidance documents (e.g., SOPs, WIs) for commissioning, qualification, cleaning, and process validation under the direction of the direct manager.
  • Comply with cGMP regulations, quality policies, procedures, and instructions as defined by the quality function and supported by site management.
  • Follow safety protocols, policies, procedures, and instructions as established by EHSS functions and endorsed by site management.

Qualifications:

  • A degree in Engineering or Life Sciences (Biology, Chemistry, etc.), such as a Dipl.-Ing., M.Sc., B.Sc., or equivalent qualification.
  • At least 3 years of experience in Qualification and Validation in a similar role, ideally within a Life Sciences, Pharma, or Biotech facility.
  • Demonstrated expertise in cGMP, Qualification, Cleaning, Process Validation, and Quality Risk Management.
  • Proficiency in English, with additional knowledge of German being a plus.
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