Key Responsibilities:

• Lead and continuously coach, guide and develop the QMS Operations Team.
• Establish and run the QMS network for GMP (Good Manufacturing Practices and GDP (Good Distribution Practices) areas and drive interactions with all functions within the commercial Operations through the defined governance model. Ensure the management of the Global Procedure Governance Board is in place and the document change management process is effective.
• Manage the QMS documentation activities to ensure the documentation in use is in compliance with processes and procedures agreed with Global QMS, including document review to ensure a high standard of documentation is in place.
• Manage and perform the required QMS Communications to the organisation
• Act as BSO (including Deputy) for ESOPS D2/ CONDOR/ CIRF/ GxP NESS; ensure the management of the backlog maintenance and system release activities. Act as the End user support  for IT systems.
• Ensure that the Periodic Review management is in place and effective to reduce the number of overdue documents within the QMS.
• Provide Audit & inspection support for QMS Operations topics.
• Act as a subject matter expert for selected Quality processes and collaborate with the respective QSO/Process owner to ensure GxP compliance of the processes and tools within own remit.
• Author/review respective QMS documentation.
• Lead and/or participate in key QMS projects or initiatives ensuring that:
  • defined quality elements and compliance requirements are addressed,
  • all required activities for successful and timely execution are completed,
  • the roll-out to impacted local entities across Novartis is achieved
• Establish and maintain community/network of Subject Matter Experts or Single Points of Contact and drive interactions with corresponding Functions. Establish strong partnership with key stakeholders.
• Create synergies and opportunities by leveraging lessons learned and communicating them to the SMEs and stakeholders as applicable.
• Participate in benchmarking activities as applicable and keep up to date with industry standards.
• Maintain knowledge of current industry trends and Health Authority expectations.

Commitment to Diversity & Inclusion: :

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

Essential Requirements:

• Education: University degree in Pharmacy, Chemistry, Engineering or equivalent related discipline preferably in Quality Systems.
• Min. 8-10 years’ experience in the pharmaceutical industry in a relevant field, such as quality assurance, quality control, registration, clinical development or manufacturing or a directly related area.
• Broad experience in QA processes and underlying regulatory requirements and industry standards/best practices.
• Fluent English, other languages are a plus.

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

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

Commitment to Diversity and Inclusion:  Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.