Global GMP Audit Lead

Sandoz; Madrid; Presencial; EUR 90.000 - 130.000; Jornada completa

Descripción de la vacante

Sandoz is seeking a GMP Senior Auditor to lead and support independent GMP audits across manufacturing sites, development centers, and suppliers. The role ensures compliance with GMP regulations, reviews corrective actions, and provides risk-based guidance to business units.

Ideal candidates hold a science degree, 10+ years in pharma/medical devices, and 3+ years auditing, with fluent English and willingness to travel about 60%.

Formación

• Degree in Chemistry, Pharmacy, Biology, Engineering or another related science.
• Advanced degree preferred.
• At least 10 years broad experience in Pharmaceutical or Medical Device Industry.
• 3 years auditing experience preferred.

Responsabilidades

• Support the strategic development of an effective global risk-based audit strategy and program.
• Plan, lead, conduct, document, and follow-up GMP audits per Sandoz Quality procedures and applicable regs.
• Assess risk of complex audits (sterile API, aseptic DP, combination products).
• Provide technical guidance, mentoring, and training on audit activities.
• Provide regulatory guidance for timely remediation and filing adequacy.

Conocimientos

Auditing

GMP knowledge

Leadership

Communication

Risk assessment

Training

Educación

Science degree (Chemistry/Pharmacy/Biology/Engineering)

Advanced degree preferred

Descripción del empleo

Sandoz is seeking a GMP Senior Auditor to lead and support independent GMP audits across manufacturing sites, development centers, and suppliers. The role ensures compliance with GMP regulations, reviews corrective actions, and provides risk-based guidance to business units.

Ideal candidates hold a science degree, 10+ years in pharma/medical devices, and 3+ years auditing, with fluent English and willingness to travel about 60%.