19 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

Proclinical is seeking a Quality Assurance Logistic Specialist to join a dynamic team in Switzerland. ... Familiarity with quality systems such as SAP and LIMS. ... Experience managing quality tools, including deviations, CAPA, and change controls. ... Ready to play a critical role in safeguarding pharmaceutical quality while driving compliance across ... Strong understanding of GMP regulations and pharmaceutical quality management systems.

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

- Minimum 5 years of experience in Quality Assurance (QA), Computerized Systems Validation (CSV), IT ... months - CSV, Quality Assurance, Data Integrity Location: Visp Initial 3 Months Contract with possibility ... Responsibilities - Must possess a comprehensive understanding of Computerized Systems Quality Assurance ... - Lead and coach QA and non QA professionals supporting computerized systems and data integrity activities ... Quality, Data Integrity, or a related quality/compliance function within a GMP-regulated pharmaceutical

• Provide Data Integrity support for deviations, investigations, change controls, CAPAs, quality risk ... • Academic degree in Life Sciences, Engineering, Information Technology, Pharmaceutical Sciences, Quality ... principles, ALCOA+, computerized systems, and applicable regulatory requirements. • Experience with quality ... manufacturing sites in the world, where reliable, complete, and accurate data is essential to ensuring product quality ... cross-functional teams. • Experience supporting Data Integrity, compliance, computerized systems, CSV, 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.

Experience as a QA trainer or trained as a trainer for Quality topics is an advantage. ... Guide and influence stakeholders by providing QA expertise, ensuring robust quality culture and operational ... Manage and actively participate in “QA on the floor” program, including QA walkdowns and GEMBA walks. ... The site in Visp, Switzerland is growing and for our Biologics Quality organization, we are currently ... What you will do: Support continuous improvement programs to establish effective Quality Management

by partnering closely with Operations, QA, QC, Central Contamination Prevention & Control Teams, Microbiology ... The Sterility Assurance Lead (SAL)(f/m/d) is responsible for leading the Sterility Assurance and Microbial ... This role owns the Contamination Control Strategy (CCS) and drives a strong sterility assurance culture ... Act as the Sterility Assurance Subject Matter Expert (SME) for facility design, technology transfers, ... Lead investigations, corrective and preventive actions, and root cause analyses related to sterility assurance

standards Manage and coordinate change control processes in collaboration with QA Align and coordinate ... cross-functional teams across operations, engineering, maintenance, and quality Monitor project progress ... mechanical adaptations and process improvements Ensure compliance with GMP regulations and internal quality

Collaboration with QC project leads, QA Analytics, as well as external clients. ... Compliance with quality, data integrity, and safety requirements. ... Support quality documentation and change management process for reference standards, including review ... Proven experience in a cGMP environment – experience in quality control or analytical development preferred

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.

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

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

Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless ... assurance environment. - Hands-on experience with electronic batch record systems (MES Syncade, DeltaV ... ) and quality management systems (TrackWise, SAP, LIMS). - Solid understanding of Good Documentation ... real-time collaboration and the technical precision needed to manufacture medicines to the highest quality ... and operator comments in strict alignment with ALCOA+ and GDP principles. - Draft clear, compliant quality

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

Lead technical oversight, contractor coordination, and quality assurance for sprinkler, deluge, dry extinguishing ... real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality

assurance and quality control. ... a crucial role in the network between the different departments such as development, manufacturing, quality ... real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality ... and cost, in compliance with the relevant laws, regulations and guidelines with view on safety, quality ... bioconjugates by being responsible for the execution of your assigned programs in the best possible time, quality