Major accountabilities:

• Collaborates to ensure that the site’s quality system is maintained compliant to regulatory and GMP compliance requirements.
• Collaborates in the management of the site’s quality systems documentation and reviews, defines updates and approves (when agreed with the quality management) site specific quality systems documents.
• Provides oversight for the implementation of Quality Systems and Regulatory Compliance including management of Non conformances, CAPAs, Effectiveness Checks, Change Controls, Training, Inspections and Audit readiness, Technical complaints, Risk Assessments and remediation, Annual Product Quality review, self-assessments, KPIs and Quality Management
  Review.
• Support the manager in the design and oversight of strategic site quality system and works in collaboration with site functions to define written procedures including but not limited to monitor and control of the manufacturing environment, training, document control/record retention, deviations/CAPA investigations, and monitoring compliance with all requirements of good
  manufacturing practice.
• Support the quality management to develop and deliver a robust overall quality system, strategy, and ultimate plan resulting in a fully compliant quality system infrastructure with respect to procedures and processes.
• Provides oversight for audit and inspection management, inspection strategies, preparation, interactions and responses.
• Support the quality team in the health authority inspection preparation and ensures key support during MOH and Novartis global audits.
• Develop Health Authority communications, including written correspondence,
  responses to inspection observations, presentations and verbal communication
• Works with quality and compliance team to ensure robust quality systems are implemented and
  sustained including, deviation/CAPA Management: Ensures all deviations from established
  procedures are appropriately documented and investigated to determine and fix root cause.
• Support escalation of Quality/cGMP issues and deficiencies to the Site QA Head and support global escalation process if needed. Support associates within the Novartis network incase of Health Authority Notifications (s.a. FAR, Rapid alert, recalls)

Minimum Requirements:

• Education: Bachelor´s Degree in Pharmacy or MSc in Pharmaceutical Industry.
• 2+ years of experience in a GxP (Bio)pharmaceutical or API manufacturing operations up of which 1+ years of experience in a Quality Assurance role.
• Excellent communication skills
• Fluent English and Spanish, written and spoken.

Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: http://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: http://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.