Audit & Compliance Professional

Novartis; Torre Annunziata; In loco; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

A pharmaceutical company in Torre Annunziata is seeking an Audit & Compliance Professional to manage GxP Compliance and audit activities, ensuring adherence to quality standards. The ideal candidate has a scientific degree and solid experience in QA Compliance within the pharmaceutical industry. Proficiency in Italian and English is required. This is a full-time position offering an opportunity to significantly impact compliance operations.

Competenze

• Solid previous experience in a QA Compliance department within the pharmaceutical industry.
• Fluent in Italian and English.
• Project management skills.

Mansioni

• Manage cost-effective GxP Compliance and Audit activities.
• Act as a Program / Project Manager for Quality Stream.
• Oversight of all production and testing activities to ensure compliance.

Conoscenze

Auditing

Audit Management

Communication Skills

Compliance Audits

Compliance Risk

Decision Making Skills

Organizational Skills

Regulatory Compliance

Risk Management

Formazione

Scientific degree

Descrizione del lavoro

Job Description Summary

The Audit & Compliance Professional manages cost effective GxP Compliance and / or Audit activities operations and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP legal and regulatory requirements and through internal audits KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators).

Performs preparation and management of external and corporate audits and Health Authority inspections.

Major accountabilities

• Act as a Program / Project Manager for the Quality Stream linked to main projects at site level.
• Act as CAPA Plan and Remediation Plan Program / Project Manager ensuring the respect of the timeline assess and prevent any potential interferences between projects and CAPA / Remediation plans.
• Oversight of all production and testing activities ensures compliance with cGxP including data integrity and eCompliance with specific focus on Quality Workstream for the main projects on site.
• Support exception investigations.
• Review and approval of production QC and AS&T records.
• Support site qualification and validation activities (planning advising review).
• Implementation of Quality Systems (incl. documentation management).
• Supplier management activities (agreements oversight audit).

Essential requirements

• Scientific degree.
• Solid previous experience in a QA Compliance department within the pharmaceutical industry.
• Project management skills.
• Fluent in Italian and English.

Skills Desired

• Auditing
• Audit Management
• Communication Skills
• Compliance Audits
• Compliance Risk
• Continued Learning
• Dealing With Ambiguity
• Decision Making Skills
• Gmp Procedures
• Inspection Readiness
• Organizational Skills
• People Management and Leadership
• Qa (Quality Assurance)
• Regulatory Compliance
• Risk Management
• Self-Awareness
• Technological Expertise

Required Experience

Unclear Seniority

Key Skills

• Abinitio
• Apprentice
• Dermatology
• Cost Estimation
• Data Networking
• Liaison

Employment Type: Full-Time

Experience: years

Vacancy: 1