pOn behalf of our Client, an international pharma company based in canton Lucerne, we are looking for an bAssociate Supply Chain Specialist, Material Compliance /b. /p pIn this role, you will work closely with above site supply chain team, local quality, tech transfer, procurement, and manufacturing operations as well as other self-directed work teams in the site’s value stream. /p h3General Information: /h3 ul libLatest start date: /b January 2027 /li libDuration: /b 1 year /li libExtension: /b possible, to be discussed /li libContract: /b temporary contract via Randstad (employment) /li libLocation: /bcanton Lucerne /li libHome office: /b possible, hybrid role /li /ul h3Tasks Responsibilities: /h3 ul liCreate and maintain supply chain records in our supplier qualification system. /li liAssess all material related changes (vendor or site initiated) and drive quality change control where needed. /li liBuild an excellent relationship with suppliers of assigned categories to ensure value is created and delivered for the site. /li liCreate material specifications as part of the material qualification activities to support material releases. /li liCoordinate material release schedule to ensure on time material availability for production /li liCollaborate with internal and external stakeholders (tech transfer, procurement, manufacturing) for material identification and supplier selection. /li liEnsure material is sourced/implemented with the required quality grades for clinical manufacturing. /li liEnsure purchase orders are placed in line with lead times to meet manufacturing schedules. /li liEnsure material planning processes meet schedule need as well as safety, quality, and cost metrics. /li liSupport supply chain team on quality and compliance related issues through investigations, change controls, quality risk assessments etc. /li liInitiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements. /li /ul h3Your profile: /h3 ul liBachelor’s or Master’s degree in engineering, pharmacy or science related field or a minimum of 3 years’ experience working in a relevant academic or industry field. /li liExperience within quality operations/ compliance or supporting supply chain or operations role within a pharmaceutical company /li liExcellent command of English, both written and verbal – ability to work within all levels of the organisation from shopfloor staff to site leadership team. /li liGood influencing / collaboration skills and teamwork mindset /li liStrong analytical and priority management skills /li liExperience in leading change management initiatives – building both people competence and introducing new processes /li liSense of initiative and overall coordination of projects and activities /li liExcellent trouble shooting and problem-solving skills, ability to challenge the status quo with a continuous improvement mindset. /li liComputer literate with advanced skills in MS Office, especially Excel /li liSAP knowledge is an advantage /li liPromoting a culture where diversity and inclusion is supported. /li liAbility and willingness to keep learning /li /ul #J-18808-Ljbffr
Associate Supply Chain Specialist, Material Compliance Arbeitgeber: Randstad Switzerland
Unser Kunde, ein globaler Pionier in der Pharmaindustrie mit Sitz in Kaiseraugst, bietet eine dynamische und unterstützende Arbeitsumgebung, die auf Innovation und Zusammenarbeit ausgerichtet ist. Mitarbeiter profitieren von flexiblen Arbeitszeiten, der Möglichkeit, im Home Office zu arbeiten, sowie umfangreichen Weiterbildungs- und Entwicklungsmöglichkeiten, um ihre Karriere voranzutreiben. Die Unternehmenskultur fördert Teamarbeit und kontinuierliches Lernen, was es zu einem hervorragenden Arbeitgeber für Fachkräfte im Bereich klinische Studien macht.
