Overseeing and conducting routine Good Manufacturing Practice (GMP) audits
Providing regulatory compliance guidance and support to the entire Quality organization
Delivering training and leading multidisciplinary teams and initiatives
Generating study protocols, reports, and standard departmental documentation
Reviewing analytical results and related processes for assigned projects
Ensuring knowledge and application of applicable working standards (GMP, SOPs, internal guidelines, GLP, etc.)
Reporting any incidents impacting normal operations to the direct supervisor

Degree in Health Sciences (Pharmacy, Biology, Chemistry, Biochemistry, Biotechnology); Master’s and/or PhD desirable
Minimum of 2 years’ experience in the pharmaceutical industry
Knowledge of GMP, GLP, ICH, and related guidelines
Availability to travel frequently (30%)
Advanced level of English (C1) – indispensable
Strong time management and prioritization skills
Excellent communication, analytical skills, and attention to detail
Strong ability to work effectively within a team

Quality Auditor

Key skills