Quality Assurance Project Lead South Cluster

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ppbBefore you apply to a job, select your language preference from the options available at the top right of this page. /b /p pExplore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrow—people with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level. /p h3Job Description: /h3 h3Location: Somaglia (Lodi) (on site, with flexibility) /h3 h3Contract: permanent /h3 h3Working hours: standard /h3 pThe Healthcare Quality Assurance Project Lead South Cluster is responsible for coordinating and supporting quality assurance activities across healthcare projects, ensuring the effective implementation and maintenance of the Quality Management System in compliance with ISO 9001, ISO 13485, EU GMP, and EU GDP requirements. /p pThe role provides quality and compliance oversight for new buildings, client implementations, equipment, processes, audits, validations, risk assessments, change controls, and process improvement initiatives, while collaborating closely with internal stakeholders and external partners to ensure robust, compliant, and efficient project delivery. /p h3RESPONSIBILITIES: /h3 ul lipCoordinate the implementation and the maintenance of the Quality Management System (QMS) in accordance with ISO: 9001 and ISO: 13485 standards, and in compliance with the EU GMP and EU GDP Guidelines. /p /li lipApplies his/her knowledge, skills and tools in assessing and supporting Projects from the quality and compliance point of view. /p /li lipCoordinate/execute various projects such as: /p /li lipSetting up the QMS in a new Building,



/p /li lipAssessment of new Client opportunities, /p /li lipImplementation of new Clients, /p /li lipImplementation of new Equipment, /p /li lipImplementation of new Processes, /p /li lipSupports External Audits within the scope of Project Management (e.g. new Client Audits, initial Regulatory Inspection). /p /li lipConducts risk assessments on QMS processes to identify and mitigate any risks. /p /li lipSupports with process validation on new processes and new Buildings. /p /li lipSupport and complete Design Qualification in a new Building and/or with new Clients. /p /li lipKeeps track of the projects, monitors the progress and identifies best practice and lessons learned. /p /li lipCoordinates process improvements projects within the applicable departments /p /li lipCreate and provide training related to Client implementation /p /li lipCreate Change Controls for any Projects where applicable /p /li /ul h3KEY INTERACTIONS /h3 h3Internal : /h3 ul lipProject Management /p /li lipOperations Management /p /li lipQA Department / Document Control Department /p /li lipSolutions / Implementations /p /li lipSecurity /p /li lipBaSe Team /p /li lipProcurement Department /p /li lipValidation Department /p /li lipIT/ FUR Department /p /li /ul h3External :



/h3 ul lipRegulatory Agencies /p /li lipClients /p /li lipSuppliers /p /li lipThird Party Auditors /p /li /ul h3QUALIFICATIONS /h3 h3Education level /h3 pBachelor's degree or International equivalent in Sciences- Required /p pPharmaceutical, healthcare or food industry experience - Preferred /p pQuality Assurance experience - Preferred /p h3Specialized Knowledge /h3 ul lipbProven experience in managing ISO: 9001 and/or ISO: 13485 standards /b /p /li lipbProven experience with GMP and/ or GDP guidelines is an advantage. /b /p /li lipbExperience with Supply Chain Industry is an advantage. /b /p /li lipbExperience with Root Cause Analysis tools (e.g. 5 why’s, FMEA) is a must. /b /p /li lipbExperience with Project Management is a must. /b /p /li /ul h3Skills /h3 ul lipbProficient in written and verbal English. /b /p /li lipbProficient in written and verbal Italian. /b /p /li lipKnowledge of Spanish is a plus. /p /li lipStrong verbal and written communication skills, to present recommendations and report back to different levels within the organization. /p /li lipPreferably experience in technical writing of documentation. /p /li lipProficiency in Microsoft Office (MS Word, Power Point, and Excel). /p /li lipKnowledge of electronic Quality Management System is an advantage. /p /li lipAbility to prioritize decisions which may have a significant risk for the company. /p /li lipAbility to create networks and collaborate with various internal and external teams. /p /li lipIdentify potential gaps in the processes and make recommendations for possible improvements. /p /li lipCoordination of improvement projects where needed. /p /li lipImplementation of new processes having a quality critical impact on the business. /p /li lipRecommend training opportunities. /p /li lipStrong organization, time management and planning skills. /p /li lipFlexible in working hours. /p /li /ul h3Employee Type: /h3 pPermanent /p pUPS is committed to providing a workplace free of discrimination, harassment, and retaliation. /p /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/81fc22