Strategic Site Quality Leader
1 mese fa
The position of Site Quality Head Strategic is available at Novartis Farmacéutica, offering a salary range of $120,000-$180,000 per year.
About the RoleThis role will inspire and empower the team to reach new heights of success for a well-established manufacturing site for solid dosage forms in Italy. By nurturing talent and fostering a positive work environment, you can unlock your team's full potential.
To ensure the delivery of top-notch products and services, the maintenance and development of robust quality assurance processes and quality control systems are paramount. These processes act as a safety net, guaranteeing that every release activity meets the highest standards of quality and reliability.
Key Responsibilities- Lead the Site Quality organization and Quality oversight of GxP site functions.
- Act as site Technical Responsible Person (Qualified Person), as appropriate.
- Ensure that Site quality risk assessments are in place, DI and eCompliance standards applied. Ensure compliance with all cGxP and all regulatory requirements for manufacturing, control, and distribution operations.
- Drive the talent agenda: lead people processes through recruitment, training, coaching, and performance to meet all operation requirements sustaining both site and quality unit competitiveness and diversity.
- Ensure that associates are qualified for a GMP task prior to independent performance.
- Role model the culture aspiration of being Curious, Inspired, and Unbossed and ensure leaders and associates are aware and aligned on expectations and hold them accountable for success of culture journey.
- Ensure overall inspection readiness for area of responsibility.
In this role, you will be part of the site crisis management team and depending on skills, expertise, and experience, can be appointed to one of the NEM roles (Novartis Emergency Management).
Additionally, you may be required to take decisions and take necessary actions within the framework of the on-call management system.
Requirements- Bachelor Degree in Chemical Engineering / Chemistry / Pharmacy or another natural science.
- 10+ years of experience in the pharmaceutical industry (Quality Assurance, Quality Control, Regulatory and/or Production).
- Fluent English and Italian, written and spoken, other languages are a plus.
- Ability to function within ambiguity and cross-functional collaboration. In-depth manufacturing processing knowledge/experience and Quality Compliance knowledge. Proven performance in Health Authority inspections.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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