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Job content

For an international pharmaceutical company located in Vispwe are looking for a:


JOB DESCRIPTION:
  • Ensure QA oversight for Cleaning Design activities to a Large Scale Cell Culture Mammalian Facility
  • Define and review CIP strategy approach with the design and CQV team according to procedure and in compliance with regulatory guidance
  • Technical lead of cleaning validation teams including communication with customers, as appropriate
  • Support / review / approve QC cleaning studies

ESSENTIAL REQUIREMENT / RELEVANT EXPERIENCE
  • Bachelor, Master degree or PhD in Analytical Science, biotechnology, chemistry or related field
  • Significant experience in the GMP regulated pharmaceutical industry; preferable in a role within the Quality Unit (QA, QC)
  • Strong background in cGMP
  • Broad knowledge in cleaning validation of biopharmaceuticals &Biologics
  • Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)
  • Excellent verbal, written and interpersonal communications skills
  • Fluency in English, German would be an advantage



START DATE: asap
END DATE: till 30.06.2023 (high probability of extension)
WORK LOCATION: 3930 Visp
WORKLOAD: 100%


INTERESTED?
We look forward to your application via our homepage or to tkarrer@payroll-house.com.

ARBEITSORT

Visp

BRANCHE

Diverse

KONTAKTPERSON

Induserv (Nordwestschweiz) AG
Karrer Thomas
Claragraben 132a
CH-4057 Basel
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Deadline: 09-06-2024

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