unisite ag is a service provider in the field of Employer Branding & Talent Management. We provide consulting services to clients in the chemistry pharmaceutical biotech medical device and life sciences industries.
Our client Solvias AG is a global cGMP Contract Research Organization (CRO) with a comprehensive portfolio of analytical services for the pharmaceutical biotech and life sciences industry.
On behalf of our client we are currently looking for a:
Quality Specialist (m/f/d) 100% 6-9 Months
Location: Kaiseraugst AG
Duration: ca. 6-9 Monate
Tasks
- Manage QC deviations CAPAs and change controls
- Conduct root cause investigations
- Maintain and update controlled documents such as SOPs test methods and forms
- Support the implementation of CAPA actions
- Ensure data integrity and proper documentation
- Perform risk assessments related to QC processes
- Monitor quality metrics and deviation trends
- Collaborate closely with QC laboratories and QA teams
Qualification
- Experience in pharmaceutical Quality Control or contract laboratory services
- Strong knowledge of GMP regulations and data integrity principles
- Experience conducting investigations and root cause analyses
- Familiarity with analytical methods and QC workflows in regulated environments
- Strong communication skills and ability to collaborate with QC and QA stakeholders
- Structured proactive and solution-oriented mindset
- Excellent documentation and technical writing skills
- Very good command of English is required German or French is a plus
Nutze diese Gelegenheit um Deine Zukunft zu gestalten wir freuen uns auf Deine Bewerbung!
unisite ag is a service provider in the field of Employer Branding & Talent Management. We provide consulting services to clients in the chemistry pharmaceutical biotech medical device and life sciences industries.Our client Solvias AG is a global cGMP Contract Research Organization (CRO) with a com...
unisite ag is a service provider in the field of Employer Branding & Talent Management. We provide consulting services to clients in the chemistry pharmaceutical biotech medical device and life sciences industries.
Our client Solvias AG is a global cGMP Contract Research Organization (CRO) with a comprehensive portfolio of analytical services for the pharmaceutical biotech and life sciences industry.
On behalf of our client we are currently looking for a:
Quality Specialist (m/f/d) 100% 6-9 Months
Location: Kaiseraugst AG
Duration: ca. 6-9 Monate
Tasks
- Manage QC deviations CAPAs and change controls
- Conduct root cause investigations
- Maintain and update controlled documents such as SOPs test methods and forms
- Support the implementation of CAPA actions
- Ensure data integrity and proper documentation
- Perform risk assessments related to QC processes
- Monitor quality metrics and deviation trends
- Collaborate closely with QC laboratories and QA teams
Qualification
- Experience in pharmaceutical Quality Control or contract laboratory services
- Strong knowledge of GMP regulations and data integrity principles
- Experience conducting investigations and root cause analyses
- Familiarity with analytical methods and QC workflows in regulated environments
- Strong communication skills and ability to collaborate with QC and QA stakeholders
- Structured proactive and solution-oriented mindset
- Excellent documentation and technical writing skills
- Very good command of English is required German or French is a plus
Nutze diese Gelegenheit um Deine Zukunft zu gestalten wir freuen uns auf Deine Bewerbung!
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