Quality Engineering Specialist
Swisslinx
Infos sur l'emploi
- Date de publication :08 janvier 2025
- Taux d'activité :100%
- Type de contrat :Durée indéterminée
- Langue :anglais (Courant)
- Lieu de travail :Visp
On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a Quality Engineering Specialist to support qualification activities for technical facilities, equipment, and systems. This is an exciting opportunity to play a key role in ensuring compliance and quality within a dynamic and collaborative environment.
Contract Type: Contract
Start Date: ASAP
Location: Visp, Switzerland
Workload: 100%
Duration: 4 months
Your Mission
* Oversee quality-related responsibilities for daily qualification activities on technical facilities, equipment, and systems.
* Support the development, review, and release of qualification documents.
* Approve qualification documents and assess change requests for relevance to the qualified state, including supporting and approving quality risk analyses (e.g., GMP-FMEA).
* Ensure deviations are investigated and addressed appropriately in deviation reports.
* Maintain compliance with legislation, authority guidelines, and customer expectations.
* Report relevant developments and trends to the QA Qualification Group Manager.
* Contribute to the formulation and development of qualification strategies and participate in continuous training.
* Support internal audits, customer audits, and official inspections as a QA representative.
Your Background
* Proven experience in the biotechnology or pharmaceutical industry.
* Expertise in QA Qualification, including knowledge of FAT/SAT/IQ/OQ/PQ processes.
* Proactive, with strong communication skills and the ability to work effectively in a multidisciplinary team.
* Fluency in English (spoken and written).
Beneficial Skills:
* Experience in risk analysis.
* German language skills.
* Familiarity with SAP, DMS, and TrackWise.
* Independent and proactive working style.
Work Flexibility: Up to 40% home office (2 days per week).
What's on Offer
* A 4-month contract with a leading global pharmaceutical company.
* The opportunity to contribute to critical qualification activities in a state-of-the-art facility.
* Exposure to high-impact projects within a multidisciplinary and collaborative team.
Contract Type: Contract
Start Date: ASAP
Location: Visp, Switzerland
Workload: 100%
Duration: 4 months
Your Mission
* Oversee quality-related responsibilities for daily qualification activities on technical facilities, equipment, and systems.
* Support the development, review, and release of qualification documents.
* Approve qualification documents and assess change requests for relevance to the qualified state, including supporting and approving quality risk analyses (e.g., GMP-FMEA).
* Ensure deviations are investigated and addressed appropriately in deviation reports.
* Maintain compliance with legislation, authority guidelines, and customer expectations.
* Report relevant developments and trends to the QA Qualification Group Manager.
* Contribute to the formulation and development of qualification strategies and participate in continuous training.
* Support internal audits, customer audits, and official inspections as a QA representative.
Your Background
* Proven experience in the biotechnology or pharmaceutical industry.
* Expertise in QA Qualification, including knowledge of FAT/SAT/IQ/OQ/PQ processes.
* Proactive, with strong communication skills and the ability to work effectively in a multidisciplinary team.
* Fluency in English (spoken and written).
Beneficial Skills:
* Experience in risk analysis.
* German language skills.
* Familiarity with SAP, DMS, and TrackWise.
* Independent and proactive working style.
Work Flexibility: Up to 40% home office (2 days per week).
What's on Offer
* A 4-month contract with a leading global pharmaceutical company.
* The opportunity to contribute to critical qualification activities in a state-of-the-art facility.
* Exposure to high-impact projects within a multidisciplinary and collaborative team.
By applying for this position, I consent to the Swisslinx Group of companies:
- storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external servers for the purpose of informing me of potential employment opportunities
- using my personal information or
- supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities
- transferring where applicable my personal information to a country outside the EEA/EFTA
I also hereby agree to the Swisslinx privacy policy (http://www.swisslinx.com/en/legal/privacy-policy) and Terms of Use (http://www.swisslinx.com/en/legal/disclaimer)
Contact
Swisslinx