PpExplore 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. /pulliGDP / GMP /liliThis role is in the UPS Healthcare Italy division which operates in the pharmaceutical logistics and distribution market. /liliOffice /liliSomaglia /liliFUTURE YOU promises strong technical /liliperformance_ /li /ulpCan you prove you’re capable of being responsible for assisting with the implementation and maintenance of the Quality Management System in accordance with ISO 9001 and 13485 standards, and in compliance with the EU GMP and EU GDP Guidelines? /ppWe’re offering a permanent contract to a skilled worker who wants to become a Quality Assurance Specialist for UPS Healthcare facility in Somaglia (Lodi), with a good level of autonomy and continuous improvement, that will be part of a team involved in issues like compliance, licenses, non-conformances investigations and audit. /ppIf you show the correct capabilities and attitude, there could be the opportunity for you to grow your career and upskill on greater level within UPS. /ph3What you’ll do /h3ulliProvide support to ensure compliance with local and regional legal requirements and regulatory authorities. /liliProvide support to ensure the license verification is performed for customers, suppliers and any other entities working within UPS facilities (Pharmacy, GMP Area etc.). /liliProvide training, ensure the training needs are met and coordinate the trainings for the staff. /liliMonitor, conduct and coordinate self-inspections to ensure compliance with GMP, GDP and ISO 9001 and 13485 requirements. /liliWhen delegated to do so by Healthcare Compliance (QA) Management or RP / QP, provide assistance in external audits. /liliParticipate and assist in supplier audits and provide evaluation of suppliers. /liliProvide support for investigation into non-conformances and customer complaints. /liliCreates Change Controls for any significant changes and communicates them internally and to clients. /liliFollow-up on all Corrective Actions and Preventive Actions (CAPAs). /liliAssist in the maintenance of documentation in accordance with the EU GMP / EU GDP Guidelines, and the relevant standards. /liliOwn / write / review Procedures, Work Instructions, and technical documents as assigned to do so. /liliEnsure that the operations performed at the facility (reception, inspection receipt, storage, picking and shipping) are made in accordance with the approved procedures / work instructions and in compliance with the EU GMP / EU GDP guidelines. /liliUnder the supervision / direction of the Healthcare Compliance (QA) Management, conducts Management Reviews. /liliProvide support for validation activities. /liliEnsure equipment calibration and maintenance program are met. /liliCollection of Temperature Data and Monitoring of the temperature environmental conditions. /liliPromote a “quality” culture within the company. /li /ulh3What you’ll get /h3ulliPermanent contract /liliCompetitive salary /liliPlenty of opportunities to progress and grow thanks to our ‘promotion from within policy’. /li /ulh3What you’ll need /h3ulliYou will have at least a /liliBachelor’s Degree in Pharmacy / Chemistry / Pharmaceutical Chemistry and Technology (CTF) /liliThe Qualified Person (QP) requirement, that is the person defined in Article 48 of Directive 2001 / 83 / EC, as amended, and Article 52 of Directive 2001 / 82 / EC and in Directive 2001 / 20 / EC. /liliThe Responsible Person (RP) is designed by the warehouse distributor with Good Distribution Practice (GDP) license (article 79 of EU 2001 / 83 / EC directive), described in the EU GDP guidelines /lili2013 / C343 / 01directive /liliof November 2013) and D. Lgs. 24.4.2006 n. 219. /liliYou should have /liliat least 2 years of experience /liliin companies such as manufacturer / laboratories / distributors of pharmaceutical products, food and feed. /liliExperience with /liliISO 9001 is required, /liliExperience with /liliISO 13485 /liliis an advantage. /liliKnowledge of GMP and / or GDP guidelines is a nice to have. /liliYou have /lilistrong Office skills /liliand in particular on /liliExcel and Power Point /liliOther than that, you’ll be able to /liliprioritize decisions /liliwhich may have a significant risk for the company, /liliidentify potential gaps /liliin the processes making recommendations for possible improvements and /liliidentify and eliminate barriers /lilito get an effective risk management and risk assessment. /liliYou’ll also need /liliadvanced oral and written English /lililanguage skills. /li /ulh3How we recruit /h3pUPS is committed to a policy of treating individuals fairly and recruiting, selecting, training, promoting and compensating based on merit, experience and other work-related criteria. We do not discriminate against any appl /p /p #J-18808-Ljbffr