Qualified Person (QP)

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ppbSalary Range: /b €43,800.00 - €81,300.00 /p h3Job Description Summary /h3 p#LI-Onsitebr/Location: Colleretto Giacosa (Ivrea), Italy /p pThis role is based in Ivrea, Italy. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. /p pWe are seeking a highly qualified and independent Qualified Person to oversee and ensure the compliance of manufacturing and quality control activities at the site, in accordance with the applicable drug manufacturing license and local regulatory requirements. /p pIn this role, the Qualified Person will independently supervise manufacturing processes and control testing activities, acting in full compliance with Article 52 of Legislative Decree No. 219 of April 24, 2006, derived from EU Directive 2001/83/EC, and subsequent amendments. The role is critical in ensuring that medicinal products meet the required standards of quality, safety, and regulatory compliance. /p pWorking closely with the Site Quality Head and Site Manager, the successful candidate will support the effective implementation, monitoring, and continuous maintenance of a GMP-compliant Quality Management System. This includes ensuring adherence to national medicines legislation, applicable regulations, internal ADACAP quality standards, approved product quality requirements, and site SOPs. /p pAs part of the Quality Assurance function, the role will provide both operational and strategic support for GMP-related activities, helping to identify, manage, and resolve quality issues while promoting a culture of compliance, accountability, and continuous improvement across the site. /p h3Major Accountabilities: /h3 ul liCertify and release medicinal product batches, ensuring manufacturing and testing are performed in compliance with applicable laws, GMP requirements, and Marketing Authorization conditions. /li liEnsure batch documentation and records are complete, accurate, properly stored, and available for inspection or upon request by Health Authorities. /li liAssess and release manufactured medicinal products in accordance with national legislation and Qualified Person responsibilities. /li liCollaborate with Quality Control and Production teams to support batch-related activities and ensure smooth,



compliant production operations. /li liReview, support, and approve quality processes including deviations, complaints, change controls, CAPAs, and related investigations. /li liImmediately escape any significant quality irregularities identified in marketed products to site management and the Italian Medicines Agency, AIFA, as required. /li liPartner with functional leaders to maintain, monitor, and continuously improve an effective GMP-compliant Quality Management System. /li liIdentify and propose technological, procedural, and organizational improvements to enhance quality, productivity, cost efficiency, and resource optimization. /li /ul h3Obligatory Requirements: /h3 ul liDegree in bPharmacy, Pharmaceutical Chemistry and Technology, CTF, Chemistry /b, or a related scientific discipline. /li liPrevious experience as a bQualified Person /b within a pharmaceutical sterile manufacturing environment. /li liQualification as an bAuthorized Qualified Person /b, in accordance with bLegislative Decree No. 219 of April 24, 2006 /b. /li liStrong understanding of GMP requirements, pharmaceutical quality systems, and regulatory expectations. /li liHigh level of quality awareness, with a proactive approach to identifying and resolving compliance-related issues. /li liExcellent collaboration and communication skills, with the ability to work effectively across Quality Control, Production, and site leadership teams. /li liAbility to support daily production operations while ensuring compliance, safety, and product quality. /li liFluency in bItalian and English /b, both written and spoken. /li /ul h3Rewards /h3 pAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. /p pThe rewards of being part of our team go far beyond base pay and incentives.



We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. /p pExpected Annual Base Salary Range for role: EUR 43,800-81,300. /p pThe salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. /p pIn addition to your base salary, you may be eligible for a performance-based premio depending on certain performance parameters. Further details will be provided during the application process. /p pPay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. /p pRead our brochure to learn more about our global total rewards offering: /p pNote: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. /p h3Commitment to Diversity and Inclusion / EEO paragraph /h3 pNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /p h3Why Novartis /h3 pHelping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? /p h3Benefits and Rewards /h3 pRead our handbook to learn about all the ways we’ll help you thrive personally and professionally: /p h3Skills Desired /h3 /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/79j2q4