Qualified Person (QP)

IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl; Ivrea; In loco; EUR 44.000 - 81.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid working options

Parental leave benefit

Wellbeing resources

Descrizione del lavoro

Novartis seeks a highly qualified Qualified Person to oversee and ensure the compliance of manufacturing and quality control activities at the Ivrea site, Italy. You will supervise manufacturing processes and control testing in alignment with GMP and regulatory requirements, reporting to the Site Quality Head and Site Manager.

You will support the implementation and maintenance of a GMP-compliant Quality Management System, ensuring adherence to national medicines legislation, product quality

Competenze

• Degree in Pharmacy, Pharmaceutical Chemistry and Technology, or related scientific discipline.
• Strong understanding of GMP requirements and regulatory expectations.
• Proven experience as a Qualified Person in pharmaceutical sterile manufacturing.

Mansioni

• Certify and release medicinal product batches in compliance with GMP and MA conditions.
• Approve batch documentation and records for inspection.
• Review and approve deviations, complaints, CAPAs, and related investigations.
• Collaborate with QA and Production to support batch-related activities.
• Escalate significant quality issues to site management and authorities.

Conoscenze

GMP knowledge

Quality systems

Regulatory expectations

Italian-English fluency

Formazione

Pharmacy degree

Authorized Qualified Person certification

Descrizione del lavoro

Job Description Summary

Salary Range: €43,800.00 - €81,300.00 Band Level 4

Location: Colleretto Giacosa (Ivrea), Italy. This 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.

We 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. In 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.

Working 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.

As 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.

Major Accountabilities

• Certify and release medicinal product batches, ensuring manufacturing and testing are performed in compliance with applicable laws, GMP requirements, and Marketing Authorization conditions.
• Ensure batch documentation and records are complete, accurate, properly stored, and available for inspection or upon request by Health Authorities.
• Assess and release manufactured medicinal products in accordance with national legislation and Qualified Person responsibilities.
• Collaborate with Quality Control and Production teams to support batch-related activities and ensure smooth, compliant production operations.
• Review, support, and approve quality processes including deviations, complaints, change controls, CAPAs, and related investigations.
• Immediately escalation any significant quality irregularities identified in marketed products to site management and the Italian Medicines Agency, AIFA, as required.
• Partner with functional leaders to maintain, monitor, and continuously improve an effective GMP-compliant Quality Management System.
• Identify and propose technological, procedural, and organizational improvements to enhance quality, productivity, cost efficiency, and resource optimization.

Obligatory Requirements

• Degree in Pharmacy, Pharmaceutical Chemistry and Technology, CTF, Chemistry, or a related scientific discipline.
• Previous experience as a Qualified Person within a pharmaceutical sterile manufacturing environment.
• Qualification as an Authorized Qualified Person, in accordance with Legislative Decree No. 219 of April 24, 2006.
• Strong understanding of GMP requirements, pharmaceutical quality systems, and regulatory expectations.
• High level of quality awareness, with a proactive approach to identifying and resolving compliance-related issues.
• Excellent collaboration and communication skills, with the ability to work effectively across Quality Control, Production, and site leadership teams.
• Ability to support daily production operations while ensuring compliance, safety, and product quality.
• Fluency in Italian and English, both written and spoken.

Rewards

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.

Expected Annual Base Salary Range for role: EUR 43,800-81,300. The 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. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process.

Pay 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. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Commitment to Diversity and Inclusion / EEO paragraph

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Why Novartis

Helping 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? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Skills Desired

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.