Visual Inspection Subject Matter Expert, Visp e/v/e/r/y/o/n/e in Raron

h3About Us /h3pten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated, stable, usable, and safe injectable treatments for patients. /ph3Your mission /h3pFull-time | Visp (5days Onsite) /ppStart Date : 01 October 2026 /ppEnd Date : 31 March 2027 /ppWe are looking for an experienced Visual Inspection Subject Matter Expert (SME) who can hit the ground running from day one to join our team onsite in Visp for 5 days a week, over a 6-month duration with a possibility of extension. /ppIn this critical role, your mission is to ensure that the visual inspection of parenteral medicinal products is performed in a regulatory-compliant, robust, and efficient manner and continuously improved. You will act as the true owner of VI processes to drive deviation and trend analyses, standardize workflows, and increase inspection robustness. By joining us, you will play a key role in inspecting CAPAs, deviations, and batch releases, while also ensuring we remain compliant with internal quality regulations. /ppYour responsibilities will include, /pulliActing as the owner of VI processes, driving deviation and trend analyses, standardizing workflows, and increasing inspection robustness. /liliDriving capacity building through the training of operators, as well as the creation and maintenance of testsets and defect libraries. /liliHandling document management, deviation, and change management. /liliSupporting New Product Introductions (NPI). /liliActing as the deputy to release preparation of batches. /li /ulh3Your profile /h3pWe are looking for someone with: /pulliDegree in technical sciences (e.g., Pharmacy, Chemistry, Biotechnology, Medical Technology, Mechanical Engineering) or equivalent professional experience. /liliExperience in a GMP environment (EU GMP, Annex 1, Data Integrity, GDocP, health authority inspections), ideally in sterile pharmaceutical manufacturing, visual inspection (manual and/or automated), Quality Assurance, or MSAT. /liliMethodological expertise in root cause analysis, CAPA, risk assessments (FMEA), and statistics/SPC; experience with Minitab/JMP is required. /liliSystem knowledge: MES/ERP (e.g., SAP/BC), eQMS (Deviations/CR/CAPA), and VI systems (lighting/optical technology). /liliExcellent German and English language skills (spoken written). /liliKnowledge of container/closure systems (vials, RTU cartridges/syringes, stoppers, crimp caps), material-induced artefacts, packaging materials, and aseptic processing. /liliAnalytical, data-driven mindset and strong problem solving skills under time pressure. /liliStrong communication and moderation skills, capable of bridging the shopfloor to management. /liliOwnership mentality, structured working style, and high results orientation. /li /ulh3Why us? /h3pWe offer a dynamic environment where you can contribute meaningfully, collaborate with exceptional minds, and unlock your full potential. /ppHere’s what sets ten23 apart: /pulliA valuable and impactful career development opportunity in an inspiring environment /liliFlexible working arrangements and environment with an open culture and diverse workforce /liliThe opportunity to work with and learn from highly qualified and experienced employees /liliOur learning and self-developing culture offers a wide range of training options /liliCompetitive pension fund plan, annual bonus, and other financial and non-financial benefit /li /ulpAt ten23 we believe in self-responsibility and mutual trust. Therefore, we will provide our employees as much flexibility as possible and limit any bureaucracy to a minimum, whilst ensuring compliance with all applicable laws. /ph3Contact /h3pFor more information and clarification, please connect Amrith ( ) from our Talent team! /p #J-18808-Ljbffr