QC Associate (d/f/m) für Michael Page in Solothurn - myjob.ch
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      09.06.2025

      QC Associate (d/f/m)

      • Solothurn
      • Festanstellung 100%

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      Michael Page

      Michael Page

      QC Associate (d/f/m)

      • International, pharmaceutical company
        • 6 months contract with extension option

      About Our Client

      Our client, an internationally renowned pharmaceutical company in the Solothurn area is recruiting. On its behalf we are now looking for a Quality Control Associate (a) starting asap, ideally July, to join their international team till end of this year.

      Depending on the selected candidate's performance and motivation, there is a possibility of an extension or a permanent take over.

      Job Description

      The QC Associate be responsible for the ordering, management and distribution of QC related reagents and consumables through all QC laboratories on site inclusive WIP and Raw material areas. The responsibilities will be around the following task areas:

      • Managing i.e. preparing, moving, shipping, QC tests, stability & retain samples including trade and GMP compliant documentation including support of day-to-day operations within the site.
      • Aliquotating & sub-sampling drug substance bags to QC samples
      • Sample Shipment: Organizing and coordinating sample shipment for raw material tailgate samples, material science tailgates, manufacturing science samples, analytical development and technical development samples as well as shipment to partner organizations and CLOs
      • Supporting day-to-day operations within the Central and WIP laboratories, including management of work orders for QC related non-analytical testing equipment like freezers
      • Ordering, management and distribution of QC related reagents and consumables through all QC laboratories on site, as well as management of QC labware.
      • Authoring, reviewing and approving complex GMP documentation (Plans, protocols, procedures, specifications, CAPAs, deviations etc.).

      The Successful Applicant

      In order to be considered for the role, the selected candidate must have:

      • Bachelor's o OR Lab Apprenticeship with 2+ years work experience in the industry
      • 1-2 years work experience in the biotech or pharma industry ideally in GMP Quality Control
      • Technical knowledge of Chemistry and Microbiology
      • Experience with aseptic work methods
      • Hands-on experience with buffer and solution preparation is an advantage
      • First experience with LabWare LIMS and Oracle is an advantage
      • Good written and verbal communication skills in English AND German (min. B1)

      What's on Offer

      The selected candidate will be part of a dynamic team and actively contribute to the discovery, development and delivery of innovative therapies to improve the lives of patients.

      Quote job ref

      JN-062025-6759905

      Job Function

      Healthcare & Life Sciences

      Specialisation

      Biotechnology

      Industry

      Healthcare / Pharmaceutical

      Location

      Solothurn

      Contract Type

      Interim

      Job Reference

      JN-062025-6759905

      Arbeitsort: Solothurn