Pharmacovigilance QA Manager

Healthcare Businesswomen’s Association; Barcelona; Híbrido; EUR 65.000 - 85.000; Jornada completa

Descripción de la vacante

A global healthcare organization is seeking a Manager for Pharmacovigilance QA in Barcelona. You will ensure compliance and quality performance in pharmacovigilance and device vigilance activities, making a significant impact on patient safety. The ideal candidate has a relevant science degree, fluency in English, and experience in the pharmaceutical industry. This is a hybrid position that offers a unique opportunity to influence quality systems and support innovation.

Formación

• Proficiency in English required, other languages is an asset.
• Demonstrated PV quality and related pharmaceutical industry experience.
• Ability to manage and objectively evaluate compliance issues.

Responsabilidades

• Support quality performance and compliance of Novartis PV activities.
• Support initiatives focused on process improvement and compliance.
• Guide the development of corrective and preventative action plans.

Conocimientos

Agility

Auditing

Audit Management

Business Partnering

Drug Development

Leadership

Quality Management

Risk Management

Vendor Management

Educación

Relevant Degree in Life Sciences or related scientific discipline

Higher degree desirable

Descripción del empleo

Job Description Summary

Step into a critical quality role where your expertise ensures the safety and integrity of global healthcare. As the Manager, Pharmacovigilance QA, you’ll provide end-to-end quality assurance oversight for Pharmacovigilance (PV) and Device Vigilance (DV) activities across Novartis. You’ll be instrumental in maintaining compliance with both local and global regulatory standards, while upholding Novartis’ commitment to excellence in patient safety. This is a unique opportunity to influence quality systems, support innovation, and make a meaningful impact on global health outcomes.

#Hybrid
Location: Barcelona, Spain

Job Description

Key Responsibilities

• Support initiatives to maintain or improve quality performance and compliance of Novartis PV activities including case processing, medical safety, risk management, Health Authority reporting, PV IT systems and device vigilance. Champion the quality mindset.
• Support initiatives focused on quality, process, and compliance improvement. Through close collaboration with business partners, identify opportunities and develop strategies aimed at simplifying processes and improving quality while ensuring compliance with applicable regulatory requirements.
• Provide quality support of transition and integration-related activities for PV and Device Vigilance systems resulting from mergers, acquisitions, and/or divestments.
• Support maintenance of the Pharmacovigilance System Master File (PSMF).
• Support training initiatives as assigned.
• Provide quality support to PS&PV and other groups/business partners involved in PV and DV activities; assist with issue identification and root cause investigations; sign-off investigation reports.
• Support Health Authority Inspections, including inspection readiness activities, conduct, and follow-up.
• Guide the development of robust and sustainable corrective and preventative action plans (CAPA) in collaboration with the responsible groups performing PV and DV activities. Monitor status of corrective and preventative actions to ensure the issues are adequately addressed, completed, and appropriately documented.
• Ensure quality and regulatory compliance issues are promptly communicated to appropriate management. Support initiatives geared towards remediation of compliance concerns; determine effectiveness of remediation activities; provide ongoing project support and governance.
• Support activities to ensure effective quality oversight, management, and support of global PV operational vendors. Support vendor quality awareness and improvement measures.

Essential Requirements

• Relevant Degree in Life Sciences or related scientific discipline; higher degree desirable.
• Proficiency in English required – spoken & written, other languages is an asset.
• Demonstrated PV/PV quality and related pharmaceutical industry and/or Health Authority experience; Device vigilance experience a plus.
• PV auditing or inspection experience and Health Authority interactions a plus.Experience in maintenance of PV and/or device Quality Management Systems a plus.
• Ability to manage and objectively evaluate compliance issues with limited supervision; good problem solving, decision making and prioritization skills.
• Quality mindset.
• Good knowledge of PV regulations, guidelines, and policies; awareness of GCP and Part 11 requirements a plus.
• Ability to operate cross-functionally and in diverse cultural environments.

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.

Skills Desired

• Agility
• Auditing
• Audit Management
• Business Partnering
• Continued Learning
• Drug Development
• Employee Performance Evaluations
• Health Authorities
• Influencing Skills
• ISO 9001
• Leadership
• Organizational Savvy
• People Management
• Qa (Quality Assurance)
• Quality Management
• Quality Management Systems (QMS)
• Risk Management
• Root Cause Analysis (RCA)
• Self-Awareness
• Stakeholder Management
• Technological Expertise
• Vendor Management