Summary Primary Location: Barcelona, Spain Relocation Support: Novartis is unable to offer relocation support: please only apply if accessible. Help shape the quality journey of innovative Radioligand Therapy products from launch through their full lifecycle.

As Product Quality

Lead, you will provide end-to-end quality leadership across a global manufacturing and testing network, partnering with cross-functional teams to safeguard product quality, regulatory compliance and continuity of supply. You will guide critical lifecycle activities, anticipate and manage product quality risks, and bring a clear, science- and risk-based perspective to complex decisions. This is an opportunity to combine your quality expertise with broad global influence, helping ensure transformative therapies reach patients reliably and with the highest standards of quality.

Key Responsibilities Lead end-to-end quality oversight for assigned Radioligand Therapy products throughout their lifecycle.

Represent Global Product

Quality in cross-functional teams, providing clear quality guidance and recommendations. Guide quality activities for launches, new markets, technology transfers, and manufacturing or testing changes. Oversee significant product quality issues, driving timely risk assessment, resolution, and escalation.

Lead cross-site change assessments, evaluating impacts on product quality, regulatory commitments, and supply. Provide quality expertise for regulatory submissions, Health Authority responses, commitments, and lifecycle changes. Identify emerging quality risks and apply science- and risk-based decision-making to complex challenges.

Support inspection readiness across the general network, including preparation, Health Authority interactions,



and follow up. Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or another relevant scientific discipline. Extensive pharmaceutical or biopharmaceutical experience in quality, manufacturing, technical operations, or other regulated activities.

Strong knowledge of current Good Manufacturing Practice and relevant global regulatory expectations. Solid understanding of pharmaceutical manufacturing, analytical testing, validation, quality control, and technology transfer.

Experience supporting product lifecycle activities, including launches, regulatory changes, transfers, and change control. Strong ability to assess complex information, communicate clear recommendations, and influence stakeholders in global cross-functional environments. 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. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable.

Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

📌 Product Quality Lead (Sabadell)
🏢 ES06 (FCRS = ES006) Novartis Farmacéutica
📍 Sabadell