Quality Control Sample & Logistics Specialist (m/f/d) 100%

Michael Page
Solothurn
1W
  • 21.03.2025
  • 100%
  • Mitarbeiter
  • Temporär
For our client, a leading international pharmaceutical company with modern offices in the canton of Solothurn, we are currently looking for a Quality Control Sample & Logistics Specialist (m/f/d) to support the trade compliance and warehouse department to ensure to be fully compliant according GMP but also legal requirements., to start immediately for the next 9 months.

Quality Control Sample & Logistics Specialist (m/f/d) 100%

For our client, a leading international pharmaceutical company with modern offices in the canton of Solothurn, we are currently looking for a Quality Control Sample & Logistics Specialist (m/f/d) to support the trade compliance and warehouse department to ensure to be fully compliant according GMP but also legal requirements., to start immediately for the next 9 months.

Description

The selected candidate will be responsible for the following task area:

  • Management (preparation, moving, shipping) of QC test, stability & retain samples including trade and GMP compliant documentation including support of day to day operations within the site.
  • Aliquotation & sub-sampling of drug substance bags to QC samples
  • Sample Shipment: Organize and coordinate 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.
  • Support 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.).

Profile

To be considered for this position, the ideal candidate must have:

  • Associate's Degree, technical degree (1-2 years), or Bachelor's Degree.
  • Prior experience in pharmaceutical or biotech manufacturing environments, preferably in GMP Quality Control.
  • Basic knowledge of Microbiology and Chemistry.
  • Skills in buffer and solution preparation are preferred.
  • Experience in aseptical working.
  • Strong organizational skills and ability to work autonomously.
  • Effective communication skills across all levels of management, peers, contractors, and external partners.
  • Proficiency in typical productivity software (Word, Excel, Outlook, etc.).
  • Preferably familiar with LabWare LIMS and Oracle systems.
  • English proficiency is a must have.

Job Offer

Excellent project to join a well-known and prestigious pharmaceutical company.

Michael Page Switzerland
Christoph Schultz