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3 jobs found in Trübbach, St. Gallen

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    • st. gallen, st. gallen
    • permanent
    We are looking for an experienced Iron Franchise CMO Management Parenteral 100% for our client Vifor Pharma in St Gallen. You will be in charge for the Quality oversight of Operations linked to the manufacturing of Parenteral Iron-based products and many more exciting tasks. Your tasks: - You manage the Quality operations linked to the manufacturing and analytical controls of Parenteral Iron Products- You support release team to get products released on time- You ensure the Q Management of related Change Controls on CMO side- You ensure the Q management of OOX for analytical controls- You ensure Q support for technical projects linked to this products portfolio- You monitor periodically the CMO performance when it comes to Q processes- You handle the complaints management and investigations for related products- You ensure the compliance of operations against regulatory dossier- Within the Parenteral products Q team, you ensure that Vifor parenteral products meet regulatory compliance as well as current quality standards over the time
    We are looking for an experienced Iron Franchise CMO Management Parenteral 100% for our client Vifor Pharma in St Gallen. You will be in charge for the Quality oversight of Operations linked to the manufacturing of Parenteral Iron-based products and many more exciting tasks. Your tasks: - You manage the Quality operations linked to the manufacturing and analytical controls of Parenteral Iron Products- You support release team to get products released on time- You ensure the Q Management of related Change Controls on CMO side- You ensure the Q management of OOX for analytical controls- You ensure Q support for technical projects linked to this products portfolio- You monitor periodically the CMO performance when it comes to Q processes- You handle the complaints management and investigations for related products- You ensure the compliance of operations against regulatory dossier- Within the Parenteral products Q team, you ensure that Vifor parenteral products meet regulatory compliance as well as current quality standards over the time
    • st. gallen, st. gallen
    • permanent
    We are looking for our client Vifor Pharma for an motivated professional in the supply chain area. You are responsible for the Global Vifor Serialization System (VSS, based on TraceLink and Laetus) and process including the global business process and partners. You report directly to the Team Lead Supply Chain & Serialization. This position can be executed on our sites St Gallen, Zurich or Villars-sur-Glâne. We are looking for a: Supply Chain & Serialization Specialist (m/w/d) 100% Your main tasks are the following:Plan and manage global serialization, track & trace changes and projects from the business side in close collaboration with the Serialization Project Team and IT, across sites and aligned with all stakeholder and in line with the company strategyResponsible that the VSS users are able to perform the tasks by providing guidance, knowledge, training and overall supportManage global documentation (SOPs, PRCs)Support local stakeholders in optimizing the use of the VSS and linked processesEU alert managementTroubleshooting in VSS
    We are looking for our client Vifor Pharma for an motivated professional in the supply chain area. You are responsible for the Global Vifor Serialization System (VSS, based on TraceLink and Laetus) and process including the global business process and partners. You report directly to the Team Lead Supply Chain & Serialization. This position can be executed on our sites St Gallen, Zurich or Villars-sur-Glâne. We are looking for a: Supply Chain & Serialization Specialist (m/w/d) 100% Your main tasks are the following:Plan and manage global serialization, track & trace changes and projects from the business side in close collaboration with the Serialization Project Team and IT, across sites and aligned with all stakeholder and in line with the company strategyResponsible that the VSS users are able to perform the tasks by providing guidance, knowledge, training and overall supportManage global documentation (SOPs, PRCs)Support local stakeholders in optimizing the use of the VSS and linked processesEU alert managementTroubleshooting in VSS
    • st. gallen, st. gallen
    • permanent
    We are looking for our client Vifor Pharma an experienced specialist for their Global Digital Quality Systems department located at their site in St Gallen. You are passionate about Analytics/Labs and IT and want to be part of an internationally known company in the pharmaceutical industry? Then we are looking for you as: Application Manager LIMS (m/w/d) 100% Your tasks: - You will be responsible for the development, implementation and continuous improvement of our Laboratory Information Management System (LIMS) according to global standards (CFR, GAMP, ICH, GxP, etc.)- You support the validation of LIMS from the business side- You support the introduction phase of LIMS on site- You create corresponding training materials- You will be responsible for the training of power and key users- You create and review manuals, work instructions and other related documentation for LIMS- You are responsible for supporting and transferring data from files and systems into the LIMS
    We are looking for our client Vifor Pharma an experienced specialist for their Global Digital Quality Systems department located at their site in St Gallen. You are passionate about Analytics/Labs and IT and want to be part of an internationally known company in the pharmaceutical industry? Then we are looking for you as: Application Manager LIMS (m/w/d) 100% Your tasks: - You will be responsible for the development, implementation and continuous improvement of our Laboratory Information Management System (LIMS) according to global standards (CFR, GAMP, ICH, GxP, etc.)- You support the validation of LIMS from the business side- You support the introduction phase of LIMS on site- You create corresponding training materials- You will be responsible for the training of power and key users- You create and review manuals, work instructions and other related documentation for LIMS- You are responsible for supporting and transferring data from files and systems into the LIMS

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