ph3Quality Assurance Engineer at Cagents. /h3pAbout the role Cagents is looking for a detail-oriented professional to join our team in Milano. You will play a critical role in managing production documentation and facilitating the transition to digital systems within a high-stakes pharmaceutical environment. /ph3Key facts /h3pLocation: Milano /ppEngagement: Tempo pieno /ph3What you'll do /h3ulliDraft, review, and maintain Master Batch Records. /liliAssist with the migration from paper-based systems to Electronic Batch Records. /liliOversee the issuance and tracking of Change Controls while collaborating with production, engineering, and validation departments. /liliEnsure all documentation remains in full compliance with GMP standards. /li /ulh3Requirements /h3ulli2 to 3 years of professional experience within a GMP pharmaceutical setting.



/liliProven background in production documentation management or Change Control processes. /liliStrong understanding of GMP regulations. /liliProficiency in English, both written and spoken. /liliStrong interpersonal skills and the ability to work effectively within a team. /li /ulh3Skills tools /h3ulliMaster Batch Records /liliElectronic Batch Records (eBR) /liliChange Control management /liliGMP compliance /li /ulh3Practical notes /h3pThe annual gross salary for this position is between 34,000 and 45,000 Euro, depending on your specific technical skills and professional background. /ppThis recruitment process adheres to the equal opportunity principles outlined in law 903/77. /p /p #J-18808-Ljbffr

📌 Quality Assurance Engineer (Italia)
🏢 Cagents
📍 Italia