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15930en
- Contract
- English, German
- Associate
- Research & Development
- Mittelland
- Healthcare & Life Sciences
Skills
Quality Control, Pharma, Biotech, GMP, cGMP, Interpersonal skills
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This vacancy has now expired
We are currently seeking an Associate II Quality Control on behalf of our client, a leading global pharmaceutical company.
Start Date: As soon as possible
Location: Solothurn
Workload: 100%
Duration: Until December 31st, 2024 (extension possible)
Work 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.)
Your Background:
- Associate degree, technical degree (1-2 years) or Bachelor’s Degree in Science or related field
- First experience in pharmaceutical or biotech manufacturing environment. Optimally prior experience within a GMP Quality Control function and experience with purchasing
quality-controlled goods.
- Fluency in English required, German is a plus but not a must.
What’s Offered:
- Opportunity to work in a dynamic and innovative environment.
- Career development and growth opportunities within a global organization.
If you are interested in this opportunity and meet the qualifications outlined above, please apply here or email veronika.nakev@swisslinx.com with your updated resume. We look forward to hearing from you!
Start Date: As soon as possible
Location: Solothurn
Workload: 100%
Duration: Until December 31st, 2024 (extension possible)
Work 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.)
Your Background:
- Associate degree, technical degree (1-2 years) or Bachelor’s Degree in Science or related field
- First experience in pharmaceutical or biotech manufacturing environment. Optimally prior experience within a GMP Quality Control function and experience with purchasing
quality-controlled goods.
- Fluency in English required, German is a plus but not a must.
What’s Offered:
- Opportunity to work in a dynamic and innovative environment.
- Career development and growth opportunities within a global organization.
If you are interested in this opportunity and meet the qualifications outlined above, please apply here or email veronika.nakev@swisslinx.com with your updated resume. We look forward to hearing from you!
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