20 qa English-speaking jobs in Canton of Valais

The QA Manager (f/m/d) within QA Analyticsis ensuring that all processes within the QC functional areas ... comply with GxP, data integrity and regulatory requirements as well with internal/external quality standards ... will do: Represent QAAnalytics in cross-functional teams and meetings RepresentQA concerns to the Quality ... As a Quality and Compliance representative for particular functional area, you are a key member in cross-functional ... teams, serving as an interface between QC and QA Operations and interact with senior stakeholders across

gene manufacturing processes, equipment, product control strategies, and low bioburden environmental assurance ... QA Validation & Qualification 1523 Canton of Valais | on site | 4 months -with potential extension ... Act as a key QA point of contact for product transfer activities and related validation strategies. ... review and approval of SOPs, protocols, reports, change controls, deviations, and other GMP records for QA

Senior QA Specialist (m/f/d) Freelance/temporary employment for a project Visp Start date: asap ... Reference number: 896900/1 Responsibilities - Provide quality oversight for the qualification of manufacturing ... identify potential risks and improvement opportunities - Ensure facilities, utilities, and related quality ... qualified and compliant state - Lead investigations of contamination events, monitoring excursions, and quality ... manufacturing environments - Strong knowledge of contamination control principles and microbiological quality

- Logistics, Quality Assurance, LIMS Location: Visp Start date: Immediately End date: 15/03/2027 ...   The QA Logistic Specialist, ensures material incoming verification and that company's materials ... - Knowledge of quality systems, especially SAP and LIMS. ... - Strong knowledge of GMP regulations and pharmaceutical quality management systems. ... - Knowledge in managing quality tools, including deviations, CAPA and change controls.

Experience in GMP environments within the biologics industry, particularly in Quality Assurance or Quality ... Be the driving force behind seamless quality assurance for a global CMO, where precision and efficiency ... Proclinical is seeking a QA Specialist to support contamination prevention and control strategies within ... Ensure facilities and quality systems comply with internal standards and applicable regulations. ... premises and utilities qualification, ensuring compliance with regulatory requirements and internal quality

The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements for manufacturing ... Identifie emerging QA relevant topics, communicate to the IBEX QA organization and work actively on their ... Represent QA in project/tech transfer organizations for new biotech manufacturing processes. ... ensuring measures for product safety, product quality & cGMP compliance are implemented. ... Solid experience in the GMP regulated pharmaceutical industry is required; preferably in a QA role.

The QA Logistics group sits within QA Supply Chain and provides key quality oversight and support for ... You will be responsible for ensuring Quality Assurance oversight of supply chain processes, warehousing ... Provide Quality Assurance oversight for supply chain and logistics operations across the site, ensuring ... Assurance and/or Production/Supply Chain/Logistics and/or Quality Control in pharmaceutical industries ... Benefits in Visp: Lonza_Visp_Benefits What you will do: Provide QA oversight for logistics, warehousing

area of Drug Product, according to cGMP guidelines, working with the manufacturing team, engineers and QA ... Responsible to establish timely and with high quality the required production documentation (preparation ... Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality ... Provides front line technical and procedural support, working with the manufacturing team, engineers and QA ... Familiarity with GMP requirements, quality procedures, SOP execution, deviations/investigations management

Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless ... Proven track record working within a GMP-regulated manufacturing or quality assurance environment. ... Partner with cross-functional teams, including Manufacturing and Quality, to investigate and resolve ... Draft clear, compliant quality impact statements and author post-production lifecycle documentation. ... Hands-on experience with electronic batch record systems (MES Syncade, DeltaV) and quality management

deviation assessments, document reviews, and process improvements in collaboration with Production, QA ... technologies by staying current with industry developments and collaborating closely with Manufacturing, QA ... including planning, supervision, and evaluation of laboratory activities, ensuring delivery against quality ... record in leading large-scale CAPEX, investment, or technology implementation projects, delivering high-quality

Schedule Governance & Quality Assurance Maintain the integrity, quality, and reliability of project

real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality ... Collaborating with Manufacturing, MSAT, QA, and Process Development teams on daily operations and troubleshooting

real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality ... Collaborating with Manufacturing, MSAT, QA, and Process Development teams on daily operations and troubleshooting

Collaborate closely with Operations, QA, Automation, and IT/OT teams to ensure seamless system integration

Align CSV strategy with QA CSV for all Biologics scope, showcasing our dedication to high standards.

Collaborate cross-functionally with production, quality assurance, and laboratory teams to ensure seamless ... Quality Control Specialist Join our team in Visp as a Quality Control Specialist for a 7-month assignment ... Background or familiarity with Quality Control processes in a GMP-regulated environment. ... Support key quality milestones by assisting during customer audits and regulatory inspections. ... real-time collaboration and the technical precision needed to manufacture medicines to the highest quality

Work closely with MSAT, Process Development, Automation, QA, IT and global data teams to align data models ... Implement and enforce data quality checks, validation rules and monitoring to ensure data reliability ... Solid understanding of data quality, lineage, traceability, governance, and compliance, ideally within

manufacturing challenges and complex production issues in close collaboration with MSAT, Production Support, QA ... real-time collaboration and the technical precision needed to manufacture medicines to the highest quality ... of process engineers, specialists, and manufacturing professionals, fostering a culture of safety, quality

Partner closely with Manufacturing, MSAT, Quality Assurance, Quality Control, Validation, Engineering ... real-time collaboration and the technical precision needed to manufacture medicines to the highest quality

Work closely with MSAT, Process Development, Automation, QA, IT and global data teams to align data models ... Implement and enforce data quality checks, validation rules and monitoring to ensure data reliability ... Solid understanding of data quality, lineage, traceability, governance, and compliance, ideally within ... real-time collaboration and the technical precision needed to manufacture medicines to the highest quality