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Qc scientist - microbiology pharma (80 - 100%)

Schönenwerd
Eurofins
Pharmaindustrie
Inserat online seit: Veröffentlicht vor 6 Std.
Beschreibung

Job Description We are looking for a QC Microbiology Scientist for driving projects that introduce and validate innovative microbiological analytical methods within our GMP-regulated QC laboratory who will contribute to the significant growth of our business in Switzerland by: Lead projects focused on the implementation of new analytical methods and new equipment into the microbiological laboratory (e.g. identification methods, utility testing). Plan and coordinate with internal (e.g. QA, customer service) and external stakeholders (e.g. supplier) Ensure compliance with GMP, regulatory guidelines, and internal quality standards. Manage project timelines, resources, and deliverables Provide technical expertise on analytical methods Prepare and review documents related to equipment qualification (URS, QP, DQ, IOQ) and method validation and tranfer (protocol, reports) Train and mentorlaboratory staff Supervision of customer projects with focus on utility qualification testing, as well as related subcontracted analytical services within the Eurofins Group Planning and organization of customer projects and related deliverables (e.g. review of technical documents, plans and validation reports) Mapping and configuration of projects in the LIMS system Ensuring that the commissioned analytical work is carried out properly and on time, as well as co-responsibility for GMP-compliant execution Approval of analysis results and reports Supervision and scientific support of ongoing customer projects and participation in the acquisition of new projects Processing laboratory deviations and root cause analyses (OOS) General process optimization and further development of the site Qualifications Completed studies in the field of life sciences (pharmacy, biochemistry, biology, ideally microbiology) At least 3 years of relevant professional experience in a regulated environment (ISO 17025, GLP, ideally GMP)

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