6 days ago

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

Visp, SwitzerlandFull-timeMid · 2-5 yearsBusiness Analyst

What you'll do

Acting as the owner of VI processes, driving deviation and trend analyses, standardizing workflows, and increasing inspection robustness.
Driving capacity building through the training of operators, as well as the creation and maintenance of testsets and defect libraries.
Handling document management, deviation, and change management.
Supporting New Product Introductions (NPI).
Acting as the deputy to release preparation of batches.

Degree in technical sciences (e.g., Pharmacy, Chemistry, Biotechnology, Medical Technology, Mechanical Engineering) or equivalent professional experience.
Experience 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.
Methodological expertise in root cause analysis, CAPA, risk assessments (FMEA), and statistics/SPC; experience with Minitab/JMP is required.
System knowledge: MES/ERP (e.g., SAP/BC), eQMS (Deviations/CR/CAPA), and VI systems (lighting/optical technology).
Excellent German and English language skills (spoken & written).
Knowledge of container/closure systems (vials, RTU cartridges/syringes, stoppers, crimp caps), material-induced artefacts, packaging materials, and aseptic processing.
Analytical, data-driven mindset and strong problem solving skills under time pressure.
Strong communication and moderation skills, capable of bridging the shopfloor to management.
Ownership mentality, structured working style, and high results orientation.

Summarised by NextRaise from the employer’s description, which follows in full below.

Ten23-health

Visp, Switzerland

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