Quality Engineering Specialist
On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a Quality Engineering Specialist. If this is you, you will be part of the team carrying out quality assurance activities on technical facilities, equipment, and systems.
Contract type - Contract
Start Date - ASAP
Location - Visp, Canton Wallis
Workload - 100%
Duration - 5 months with possible extension
Work type - hybrid, 60% on site
Your mission:
â?¢ Holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems
â?¢ Supports the development, reviews and releases qualification documents.
â?¢ Approves applicable qualification documents
â?¢ Assesses and approves change requests with regard to their relevance to the qualified state condition and ensures this supports and approves quality risk analysis (e.g. GMP-FMEA)
â?¢ Ensures that deviations are appropriately investigated and addressed in deviation reports processed in deviation reports
â?¢ QA activities follow legislation, authority and customer expectations.
â?¢ Informs the Group Manager QA Qualification about relevant developments and trend
â?¢ Actively supports the formulation and further development of qualification strategies and continues to training accordingly
â?¢ Supports internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative (SME)
Your background:
â?¢ Experience in biotechnology or pharmaceutical environment
â?¢ Experience as QA Qualification
â?¢ Knowledge on FAT/SAT/IQ/OQ/PQ
â?¢ Experience in risk analysis is an advantage
â?¢ Knowledge of SAP, DMS and TrackWise is an advantage
â?¢ You are proactive, with good communication skills and are able to work in a multidisciplinary team towards a common goal.
â?¢ You are fluent in English (spoken and written), German is an advantage
What's on offer
â?¢ An initially 5 month contract.
â?¢ A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
Contract type - Contract
Start Date - ASAP
Location - Visp, Canton Wallis
Workload - 100%
Duration - 5 months with possible extension
Work type - hybrid, 60% on site
Your mission:
â?¢ Holds all quality related responsibilities for daily qualification activities on technical facilities, equipment and systems
â?¢ Supports the development, reviews and releases qualification documents.
â?¢ Approves applicable qualification documents
â?¢ Assesses and approves change requests with regard to their relevance to the qualified state condition and ensures this supports and approves quality risk analysis (e.g. GMP-FMEA)
â?¢ Ensures that deviations are appropriately investigated and addressed in deviation reports processed in deviation reports
â?¢ QA activities follow legislation, authority and customer expectations.
â?¢ Informs the Group Manager QA Qualification about relevant developments and trend
â?¢ Actively supports the formulation and further development of qualification strategies and continues to training accordingly
â?¢ Supports internal audits in accordance with the internal audit plan, at customer audits and official inspections as QA representative (SME)
Your background:
â?¢ Experience in biotechnology or pharmaceutical environment
â?¢ Experience as QA Qualification
â?¢ Knowledge on FAT/SAT/IQ/OQ/PQ
â?¢ Experience in risk analysis is an advantage
â?¢ Knowledge of SAP, DMS and TrackWise is an advantage
â?¢ You are proactive, with good communication skills and are able to work in a multidisciplinary team towards a common goal.
â?¢ You are fluent in English (spoken and written), German is an advantage
What's on offer
â?¢ An initially 5 month contract.
â?¢ A great opportunity to develop your career at a leading international biotechnology company.
If this sounds like you, donâ??t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: Write an email.
Über die Firma
