Descripción
---base:meta-keywords:meta-viewport: width=device-width, initial-scale=1.0title: Senior QA Specialist--- Senior QA Specialist====================Are you looking to make a meaningful impact on cutting\-edge pharmaceutical manufacturing? Join our dynamic team in Visp to champion quality excellence, tech transfer, and operational compliance in our state\-of\-the\-art facility.This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.**What you will get:*** An agile career and dynamic working culture.* An inclusive and ethical workplace.* Competitive hourly rate.**What you will do:*** Drive project\-specific QA operational oversight during commissioning, qualification, and tech transfer activities.* Make timely, risk\-based decisions on shop\-floor events and deviations to ensure continuous cGMP compliance.* Review and approve critical GMP production and batch records in accordance with approved procedures.* Assess, manage, and mitigate quality risks impacting routine GMP manufacturing using structured tools like FMEA.* Partner closely with cross\-functional teams across Manufacturing, Engineering, and Quality Control to align and execute planned milestones.* Participate actively in facility walkthroughs, internal audits, and regulatory inspections.* Serve as a quality mentor and trusted operational advisor on the production floor.**What we are looking for:*** Bachelor of Science in Life Sciences or a related field (or equivalent 3\- 4 years of relevant industry experience).* Proven Quality Assurance or operational compliance experience within a regulated pharmaceutical cGMP environment (pharmaceutical background is essential* Demonstrated experience supporting shop\-floor manufacturing, qualification, or technical transfer projects.* Practical knowledge of quality risk management methodologies (e.g., FMEA) and electronic qual