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Quality assurance specialist

Zoppola
Belimed Life Science
Pubblicato il 12 giugno
Descrizione

PpSteelco and Belimed have joined forces to lead the way in advanced cleaning and sterile workflow solutions. This partnership is powered by our united strengths: a dynamic product range, relentless innovation, utmost reliability, and an unmatched commitment to customer satisfaction. As SteelcoBelimed, we “Innovate with confidence”, as we set new industry standards to meet our customer’s needs offering high-quality products and comprehensive services for Infection Control and Life Science. /p h3Your Activities /h3 pMaintaining the QMS in compliance with relevant standards by supporting process managers in implementing applicable requirements, participating in company projects, drafting procedures and operating instructions, monitoring and controlling processes, and identifying opportunities for improvement. /p h3Tasks Responsibilities /h3 ul liConducting and participating in internal audits and managing the results. /li liSupporting the QA Manager in managing second- and third‑party audits and their results. /li liPeriodically analyzing and supporting in the definition and coordination of CAPA actions related to the QMS. /li liSupporting the management of the Change Control process related to the QMS. /liliIssuing QMS documents and managing their distribution. /li liSupporting functions managers in defining, monitoring, and continuously improving processes in accordance with relevant standards, and in drafting QMS documents within their scope of responsibility. /li liSupporting the conduct of audits and assisting in the selection, evaluation, and monitoring of suppliers. /li liSupport in activities related to customer complaints. /li liSupport the QA Manager in analyzing training needs regarding quality requirements, and in coordinating and conducting training and awareness activities for company departments. /li liProvide support and monitoring for customer projects where applicable. /li liParticipate in company projects to assess risks and their impact on the QMS and manage related activities. /li /ul h3Your Profile /h3 h3Skills Competencies /h3 ul liRegulatory and quality expertise: GMP (Good Manufacturing Practices), ISO 9001 and ISO 13485. /li liExcellent knowledge of Adobe Acrobat and Microsoft 365, particularly Word, Excel, Visio, Power BI and SharePoint. /li liPrevious experience in project management and executive reporting. /li liAdvanced level of English, both written and spoken. /li liPrevious experience in conducting internal and/or external audits. /li liStrong team-oriented and collaborative mindset. /li liExcellent public speaking skills. /li liStrong organizational skills and ability to manage priorities. /li liFlexibility, reliability, and strong mediation skills. /li /ul h3Required Experience /h3 pPrevious experience in this role is required, preferably in international companies in the pharmaceutical/medical industry or similar sectors. /p h3Required Education /h3 pA Bachelor’s degree and/or Master’s degree, or another qualification recognized by the Italian State, in Pharmacy, Engineering, or related fields. /p h3Our Offer /h3 ul liWork in an international, fast-growing industry that makes a real impact on healthcare and pharmaceutical industry. /li liBe part of an innovative and open-minded team. /li liJoin a company with a strong reputation and long-standing expertise in cleaning and disinfection solutions. /li liWe offer a people-focused work environment, with dedicated benefits and welfare initiatives. /li /ul /p #J-18808-Ljbffr

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