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Quality Control Associate (M/F/D)
Tasks:
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.)
Qualification:
Dual Language preferred with a preferences for German and English. For English min. B1 is required
Associate’s Degree, technical degree (1-2 years), or Bachelor’s Degree.
The ideal candidate has introductory experience in the pharmaceutical or biotech manufacturing sector, preferably with prior engagement in a GMP Quality Control role and familiarity in procuring quality-controlled goods
Additionally, you possess fundamental knowledge of Microbiology and Chemistry, along with experience in aseptic work environments
Preferred skills in buffer and solution preparation.
Strong organization skills and ability to work autonomously
Optimally have know-how with LabWare LIMS and Oracle system
Requirements:
Start: asap
Duration: 8 months
Capacity: 5 days per week
Location: Greater Solothurn Area
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