15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | Verification plans based on criticality and data. Cleaning CPV (Continued Process Verification) Developing a strategy for CPV implementation, including identifying guidelines, parameters for monitoring, and drafting a routine plan for biotech process cleaning methods. Quality Assurance Adhering to cGMP
Später ansehen15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | Of cleaning verifications, in collaboration with the Braine site, and updating relevant procedures and plans accordingly. Quality Assurance Committing to cGMP requirements, timely training, and ensuring that documentation is authorized, uptodate, and ready for inspection. Health, Safety, and Environment
Später ansehen15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | With UCB Technical Operations and other UCB teams. This position will ensure compliance to Medical Devices regulations, ISO requirements and GMP/cGMP compliance from a quality, safety and efficacy point of view. What you'll do Provide expert advice, support and management for technical operational QA
Später ansehen15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | Stream) your role is to oversee all aspects of DS and DP pharmaceutical production for the Product Stream Allergy. You will lead the establishment of a stateoftheart operations processes to deliver compliant and robust pharmaceutical API and DP (quality, time, process reliability and HSE
Später ansehen15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | Manufacturing Operations Lead you will manage biological Contract Manufacturing Organizations (CMOs) to ensure the supply of biological Drug Substances with the required quality, quantity, timing, and cost, following established quality and manufacturing agreements. Who you'll work with Reporting to the Head
Später ansehen15.03.24 | Vollzeit | Bulle | TipTopJob Switzerland | Stream) your role is to oversee all aspects of DS and DP pharmaceutical production for the Product Stream Allergy. You will lead the establishment of a stateoftheart operations processes to deliver compliant and robust pharmaceutical API and DP (quality, time, process reliability and HSE
Später ansehen14.03.24 | Teilzeit, Vollzeit | Lausanne | Michael Page InternationalIn the Zurich area, is looking for a Quality Assurance Specialist (m/f/d) to start immediately in a temporary assignment until end of December 2024, with a possibility for an extension or a permanent take over. - Internationally operating company - Temporary assignment to start immediately Save Job - Geneva
Später ansehen04.03.24 | Vollzeit | Gruyères | Randstad Schweiz AGParticipate to the global transfer strategy (write validation/verification plans, protocols and reports. Ensure the review) - Write analytical procedures, risk analyses and any other quality document, - Take part in activities related to lifecycle management, - Transfer analytical knowledge to the QC
Später ansehen03.03.24 | Vollzeit | Cugy (FR) | mageba saAnd Area Management, he/she leads business development activities and defines market strategies. Key objectives and purpose is to develop in-depth knowledge of and strong reputation in the markets, allowing mageba to perform as a key supplier for local stakeholders. This function is located at our
Später ansehen25.02.24 | Vollzeit | Cugy (VD) | mageba saAnd Area Management, he/she leads business development activities and defines market strategies. Key objectives and purpose is to develop in-depth knowledge of and strong reputation in the markets, allowing mageba to perform as a key supplier for local stakeholders. This function is located at our
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