Pharma Quality Validation Specialist

Stevanato Group; Piombino Dese; In loco; EUR 30.000 - 40.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health coverage

Canteen services

Flexible benefits platform

Wellbeing initiatives

Language training

Descrizione del lavoro

Stevanato Group is seeking a Validation professional to drive qualification and validation activities in a GMP environment. You will support method validation, data analysis, and cross‑functional collaboration with Commercial, R&D and production teams to ensure product quality and regulatory compliance.

The role requires a Scientific Master’s Degree and 2+ years in Validation within a multinational setting, preferably pharma/medical devices, plus knowledge of GMP and regulatory standards.

Competenze

• Requires scientific Master’s degree and 2+ years validation experience in a multinational, preferably pharma/med devices.
• Knowledge of internal audit processes, techniques and requirements.
• Familiarity with regulatory standards and global manufacturing practices (ICH, GMP, etc.).
• Understanding of legal and standard requirements linked to applicable standards.

Mansioni

• Execute qualification and validation activities per approved plan and ensure GMP compliance.
• Support definition and documentation of validation activities and review third‑party reports.
• Provide technical validation support to Commercial, R&D and other functions and transfer/validate analytical methods.
• Author/review analytical method validation protocols and reports.
• Define validation strategies and acceptance criteria for analytical methods and perform method lifecycle data analysis.

Conoscenze

2+ years validation experience

Internal audit knowledge

Regulatory knowledge

Legal and standard requirements

Good English proficiency

IT Tool literacy

Formazione

Scientific Master’s Degree

Strumenti

IT Tool

Descrizione del lavoro

Stevanato Group is seeking a Validation professional to drive qualification and validation activities in a GMP environment. You will support method validation, data analysis, and cross‑functional collaboration with Commercial, R&D and production teams to ensure product quality and regulatory compliance.

The role requires a Scientific Master’s Degree and 2+ years in Validation within a multinational setting, preferably pharma/medical devices, plus knowledge of GMP and regulatory standards.