Chief Quality Integration Specialist

hace 2 días


Barcelona, Barcelona, España Novartis A tiempo completo

About the Opportunity

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We are seeking a highly skilled Chief Quality Integration Specialist - Global In-Licensing and Mergers to lead our end-to-end Evaluation of In-licensing (BD&L) and Merger/Acquisition (M&A) up to the Integration of acquired or in-licensed assets into our network.

This role requires facilitation of timely decision making by QA Management, including relevant line functions based on recommendations from QA SMEs and business evaluation for holistic QA assessment covering due diligence evaluation as well as QA integration activities for potential external opportunities.

Key Responsibilities

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  • Establish and lead cross-functional teams and act as single point of contact for BD&L DD QA and support QA easements for corporate M&A and integration as required.">
  • Ensure representation of QA SMEs from all necessary functions.">
  • Ensures comprehensive due diligence assessments across all QA LF and timely recommendation to BD&L and M&A.">
  • Establish a robust Quality Integration plan with QA Line functions, members of the Quality Integration Team, and collaboration with the Quality organization at the acquired company or at the licensing partner.">
  • Ensure that risk mitigation measures from Due Diligence reports and related Quality risk analyses are included in the Quality Integration Plan.">
  • Ensure that Novartis' Quality Management Systems and applicable GxP rules are embedded in acquired or in-licensed assets.">
  • Coordinate and compile the data for the development of the Quality Integration Budget for integration of an acquired or in-licensed asset.">
  • Ensure open and effective communication and business partnership with all stakeholders.">
  • Oversee the implementation and handover of deals by QA SMEs to the relevant LF.">
  • Provide the Quality and Technical expertise needed in the Quality Integration process.">
  • Prioritizes, resolves issues and ensures alignment with QA LF head, including escalation to management.">
  • Represent QA at BD&L DD relevant forums including but not limited to, BD&L/M&A integration Quality Review Boards (QRBs), deputize for Global Head Business Development QA where required.">
  • Support Health Authority Inspection readiness programs as well as internal/external audits.">
  • Contribute to the continuous improvement within area of responsibility.">
  • Demonstrate proven leadership and accomplishments in an international matrix organization.">
  • Fluent spoken and written English.">
  • Broad understanding of global expectations of health Authorities in GxP regulated areas.">
  • 5 or more years of demonstrated leadership and accomplishments in an international matrix organization.">
  • Minimum 15 years' experience in the pharmaceutical industry, including operative experience in QA, Production/Technical Operations, including at least 5 years in Quality.">
  • Demonstrated GxP experience.">
  • Education: Graduate in Chemistry, Pharmacy/Biotechnology, Microbiology or another related science or equivalent experience.">
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Benefits

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We offer a competitive salary of approximately €110,000 per year, which is commensurate with your skills and experience. Our comprehensive benefits package includes:

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  • A market-leading salary.">
  • A performance-related bonus.">
  • A generous pension scheme.">
  • 25 days annual leave.">
  • A flexible working environment.">
  • Professional development opportunities.">
  • Access to cutting-edge technology and tools.">
  • A diverse and inclusive work environment.">
  • Opportunities for career progression.">
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Why Choose Novartis?

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We are committed to building diverse teams, representative of the patients and communities we serve. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

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Join us and be part of a team that is shaping the future of healthcare.

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Our products have touched the lives of over 236 million people worldwide in 2022. We believe that the answers to improving and extending even more people's lives lie in curious, courageous, and collaborative people like you.

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We empower our employees to take smart risks, explore the power of digital and data, and collaborate with others to tackle the world's toughest medical challenges.

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Location

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This role is based in Spain, specifically in Barcelona Gran Vía.

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Functional Area

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Quality

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Job Type

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Full-time

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Employment Type

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Regular



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