← Toutes les offres
TI

QA Engineer – Fill & Finish (m/f/d)

Tech'Firm Industrie AG

Basel, Bs
CDI
Publié le 13 novembre 2026 · Expire le 13 décembre 2026

Description du poste

QA Engineer – Fill & Finish (m/f/d) 🚀 Take the next step in your pharmaceutical engineering career with Techfirm Engineering! We are currently looking for an experienced QA Engineer – Fill & Finish (m/f/d) to contribute to exciting projects within the Swiss pharmaceutical industry. Are you an experienced Quality Assurance professional with a strong background in aseptic Fill & Finish operations? Do you thrive in highly regulated GMP environments and enjoy supporting manufacturing teams while ensuring the highest quality standards? Then this could be the perfect opportunity for you! 📍 Location: Near Basel, Switzerland Additional information regarding the project location and working arrangements will be provided during an initial conversation. 🎯 Your Mission As part of this assignment, you will play a key role in providing Quality Assurance support to sterile pharmaceutical manufacturing operations, with a particular focus on aseptic Fill & Finish processes. Your main responsibility will be to ensure that manufacturing activities are performed in compliance with applicable GMP requirements, internal quality standards and regulatory expectations. Working closely with Production, QC Microbiology, Engineering and Validation teams, you will provide hands-on QA support, oversee critical manufacturing activities and contribute to the resolution of quality-related issues. You will play an important role in maintaining product quality, ensuring GMP compliance and supporting the reliability of sterile manufacturing operations. 🔬 Your Responsibilities - Provide operational Quality Assurance support to sterile pharmaceutical manufacturing activities, particularly within aseptic Fill & Finish operations. - Perform QA oversight of manufacturing activities and provide quality guidance to Production teams on the shop floor. Review and approve GMP documentation, including batch manufacturing records, SOPs, protocols and reports. - Ensure compliance with EU GMP Annex 1 and applic