ph3Experteer Overview /h3pIn this role you ensure GCP compliance across Global RD by managing CAPAs, quality metrics, and audit programs. You will drive the documentation and process controls that support audit readiness and supplier qualification. You work closely with cross-functional teams to sustain a robust quality system and enable compliant clinical trials. The position offers a hybrid setup at the Parma HQ within a values-driven, sustainability-minded organization. /ph3Responsibilities /h3ulliManage GCP CAPA plans and follow-up /liliCoordinate collection of quality metrics and KPIs for Global RD /liliOversee Trackwise, supplier,



and audit workflows /liliSupport external consultants in the Auditing Supplier Qualification Unit /liliFinalize Quality Documents for the unit /liliWrite/Review SOPs related to audit and qualification of clinical service providers /liliProvide training on relevant activities and procedures /liliEnsure documentation traceability and audit report finalization /li /ulh3Qualifications /h3ulliAt least 3 years of experience in Pharmaceutical, Consultancy, or CRO in Quality Assurance for RD with strong GCP knowledge /liliKnowledge of GCP requirements and quality systems /liliUnderstanding of the pharmaceutical development process supporting clinical trials /liliExperience with training techniques /liliScientific degree /liliGood knowledge of English /li /ulh3Benefits /h3ullipension /liliprivate medical insurance /liliwellbeing programme /liliflexible benefits programme /liliremote work options /lilirelocation support /li /ul /p #J-18808-Ljbffr

📌 GCP specialist R&D Auditing Department (Parma)
🏢 Experteer Italy
📍 Parma