Définir une nouvelle alerte d’emplois
Définir une nouvelle alerte d’emplois
Entrez votre adresse e-mail ci-dessous pour recevoir des alertes dans votre boite mail lorsque des offres similaires seront disponibles.
En cliquant sur « Oui, envoyez-moi des offres » ci-dessous, vous acceptez de recevoir des offres dans votre boîte mail qui correspondent aux critères de recherche que vous avez sélectionnés, comme indiqué dans notre politique de confidentialité.
En cliquant sur « Oui, envoyez-moi des offres » ci-dessous, vous acceptez de recevoir des offres dans votre boîte mail qui correspondent aux critères de recherche que vous avez sélectionnés, comme indiqué dans notre politique de confidentialité.
Merci d’avoir créé une alerte d’emploi
16426en
- Contract
- English
- Associate
- Research & Development
- Switzerland
- Healthcare & Life Sciences
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is seeking a Quality Engineering Specialist to take on quality-related responsibilities for technical facilities, equipment, and systems. If you have a strong background in qualification activities and thrive in a dynamic, GMP-regulated environment, this could be an excellent opportunity for you!
Contract type: Contract
Start Date: ASAP
Location: Visp, Canton Wallis
Workload: 100%
Duration: 6 months
Your Mission
As a QA Qualification Specialist, you will play a key role in ensuring that all qualification activities meet regulatory and quality standards.
Your key responsibilities will include:
• Overseeing and ensuring the quality of daily qualification activities for technical facilities, equipment, and systems.
• Supporting the development, reviewing, and releasing of qualification documents.
• Approving qualification documents, change requests, and quality risk analyses (e.g., GMP-FMEA).
• Investigating and addressing deviations in deviation reports.
• Ensuring QA activities adhere to legislation, regulatory authority requirements, and customer expectations.
• Informing the Group Manager QA Qualification about relevant developments and trends.
• Supporting the development and continuous improvement of qualification strategies and related training.
• Acting as QA representative during internal audits, customer audits, and official inspections.
Your Background
• Experience: Previous experience in a QA qualification role within the biotechnology or pharmaceutical industry.
• Knowledge: Expertise in FAT/SAT/IQ/OQ/PQ processes.
• Skills: Proactive, with strong communication skills and the ability to work collaboratively in multidisciplinary teams.
• Languages: Fluent in English (spoken and written); German is a plus.
• Beneficial Skills:
• Experience with risk analysis.
• Familiarity with SAP, DMS, and TrackWise.
• Independent and proactive work ethic.
What’s on Offer
• A dynamic 6-month contract role within a globally renowned biotechnology company.
• The possibility of up to 2 days of home office per week.
• An exciting opportunity to further develop your expertise in a cutting-edge environment.
If this sounds like the right fit for you, don’t hesitate to apply! For more information, please reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
Contract type: Contract
Start Date: ASAP
Location: Visp, Canton Wallis
Workload: 100%
Duration: 6 months
Your Mission
As a QA Qualification Specialist, you will play a key role in ensuring that all qualification activities meet regulatory and quality standards.
Your key responsibilities will include:
• Overseeing and ensuring the quality of daily qualification activities for technical facilities, equipment, and systems.
• Supporting the development, reviewing, and releasing of qualification documents.
• Approving qualification documents, change requests, and quality risk analyses (e.g., GMP-FMEA).
• Investigating and addressing deviations in deviation reports.
• Ensuring QA activities adhere to legislation, regulatory authority requirements, and customer expectations.
• Informing the Group Manager QA Qualification about relevant developments and trends.
• Supporting the development and continuous improvement of qualification strategies and related training.
• Acting as QA representative during internal audits, customer audits, and official inspections.
Your Background
• Experience: Previous experience in a QA qualification role within the biotechnology or pharmaceutical industry.
• Knowledge: Expertise in FAT/SAT/IQ/OQ/PQ processes.
• Skills: Proactive, with strong communication skills and the ability to work collaboratively in multidisciplinary teams.
• Languages: Fluent in English (spoken and written); German is a plus.
• Beneficial Skills:
• Experience with risk analysis.
• Familiarity with SAP, DMS, and TrackWise.
• Independent and proactive work ethic.
What’s on Offer
• A dynamic 6-month contract role within a globally renowned biotechnology company.
• The possibility of up to 2 days of home office per week.
• An exciting opportunity to further develop your expertise in a cutting-edge environment.
If this sounds like the right fit for you, don’t hesitate to apply! For more information, please reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
.jpg)
I manage this role