10 qa-Stellen in Bitsch heute aktualisiert
Stellenangebote gefunden
Eupro AGppbVisp, Valais, Switzerland /b /p pb100% On-site (5 days/week) /b /p pb6-Month Renewable Contract /b /p pbStart Date: September 2026 /b /p h3About the Opportunity /h3 pOur client, an international company operating in the biopharmaceutical sector, is currently looking for an experienced bQA Logisti
Eupro AGpEupro AG in Visp, Valais, Switzerland, is seeking a QA Logistics Materials Specialist to join its Quality organization on a 6-month renewable contract starting September 2026. This on-site role focuses on material management, incoming material verification, and GMP-compliant quality activities. /pp
ppJoin a transformative GMP expansion project and make a lasting impact through validation, compliance, and quality excellence. /p pProclinical is seeking a QA Validation Specialist to support a major expansion project in Switzerland. This role focuses on ensuring that GMP equipment, facilities, and
pProclinical Staffing is seeking a QA Validation Specialist to support a major expansion project in Switzerland. You will ensure GMP equipment, facilities, and systems are qualified, validated, and maintained in compliance with regulatory standards, working with operations, engineering, and regulato
ppSwitzerland, Visp /p pbLocation: /bthe actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. /p pYou will support the QA topic of facility operation as well as pest control within the CPC (Contamination Preven
Gi GroupppFor our client, a global leader in biopharmaceutical manufacturing, we are seeking an experienced /ppbQA Validation Specialist (m/w/d) /b /ph3General Information /h3ullibStart Date: /b /lilibDuration: /b until /li /ulh3Tasks Responsibilities /h3ulliPerform QA oversight of qualification and validat
Gi GrouppGi Group is seeking an experienced QA Validation Specialist for a global leader in biopharmaceutical manufacturing in Switzerland. You will oversee qualification and validation activities to keep GMP equipment, facilities and systems in a validated state. /ppResponsibilities include reviewing SOPs,
BioTalentpBioTalent, a global biotechnology organisation, is seeking a QA Validation Specialist to support a major facility expansion. The role focuses on QA oversight of qualification and validation activities within a GMP-regulated environment. /ppYou will manage QA oversight, review validation documentati
pLonza in Visp, Switzerland, is seeking a Senior QA Specialist for Process Validation. You will ensure validation compliance for small molecules, lead validation activities at manufacturing scale, and support continued process verification and PQR activities. /ppThe role emphasizes collaboration acr
pLonza in Visp, Switzerland, is seeking a Senior QA Specialist for Cleaning Validation at 80-100%. The role supports the full validation lifecycle, reviews validation docs, and collaborates with Development teams to ensure GMP-compliant processes. Relocation assistance is available for eligible cand
Job Description As a QA Logistic Specialist, you will ensure that incoming materials are verified and qualified in accordance with applicable GMP requirements, corporate standards and established service agreements. Based onsite in Visp five days per week, you will oversee the quality and compliance
AdryanQA Logistics Specialist Duration: Immediately until March 2027 Location: Visp, 5 days onsite About the role: QA Logistics Specialist ensures material incoming verification and that materials qualification process and services associated, are aligned with regulatory requirements corporate standards a
EFORQA Validation Specialist In 13 years, the EFOR Group has reached the leading position in Life Sciences consulting with strong, synergic and strategic acquisitions. Our ambition is to build a global leading position of our market in 2028. Today, we are an innovative organization working with passiona
Join a transformative GMP expansion project and make a lasting impact through validation, compliance, and quality excellence. Proclinical is seeking a QA Validation Specialist to support a major expansion project in Switzerland. This role focuses on ensuring that GMP equipment, facilities, and syste
Join a transformative GMP expansion project and make a lasting impact through validation, compliance, and quality excellence. Proclinical is seeking a QA Validation Specialist to support a major expansion project in Switzerland. This role focuses on ensuring that GMP equipment, facilities, and syste
Our client, pharmaceutical company in Visp, is looking for a QA Validation Specialist: Role Title: QA Validation Specialist I (Qualifications) Contract Duration: ASAP – December 31, 2026 Location: Visp (CH) Role Overview The QA Validation Specialist I provides QA oversight for Commissioning, Qualifi
Job Description Location: Visp, Switzerland (onsite) Role Overview The QA Validation Specialist will report to the Head of QA Validation & Qualifications. The role will be part of a small core team consisting of permanent employees and this fixed-term contract position. The specialist will work
HaysGeneral information: Start date: asap End date: 31.12,2026 Location: Visp, on site Key responsibilities Must possess a full grasp of the duties of Qualifications (CQV) and Validation. Perform QA oversight of the Validation review and qualification activities to ensure GMP equipment, facility and/or
We are looking for an experienced QA Validation Specialist to support qualification and validation activities within a GMP-regulated environment. This role is responsible for ensuring equipment, facilities, and systems remain compliant, qualified, and maintained in a validated state while supporting
CHF 38'000 – CHF 61'000/Jahr
Schatzungsvertrauen: Niedrig
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