Quality & Regulatory Compliance Officer

7 giorni fa


Lazio, Italia Adecco Italia Spa A tempo pieno

Freelance Quality Compliance Specialist – Pharmaceutical Sector (Latina, Italy) Location: Latina, Italy (100% On-site) Work Model: Full-time, Freelance Contract Available Sector: Pharmaceutical Manufacturing Languages Required: English & Italian #We are seeking a Quality Compliance Specialist with hands-on experience in sterile process management to support a leading pharmaceutical company in Latina.This is a fantastic opportunity for professionals looking to contribute their expertise in a dynamic, compliance-driven environment.Freelancers are welcome to apply#Manage sterile process deviations, including writing and reviewing deviations and complaints.Review Annual Product Reviews (APRs) and handle quality complaints, including investigations, reporting, CAPA definition, and follow-up.Lead change control processes: evaluate, define activities with relevant teams, and monitor progress.Support production technologies with quality compliance: write/review APS protocols, PPQ batch records, and PPQ protocols/reports.Utilize TrackWise (preferred) for electronic quality management.#2–5 years of specific experience in Quality Compliance within sterile pharmaceutical processes.~ Solid knowledge of complaint management, CAPA processes, and change controls.~ Familiarity with TrackWise or similar electronic quality management systems is a plus.~ Full-time availability: Monday to Friday, 08:*******:00.#Opportunity to work with a well-known pharmaceutical company in Latina.Freelance contract option for independent professionals.If you're a proactive professional with a passion for quality compliance in sterile pharmaceutical processes, we'd love to hear from you.Apply now and bring your expertise to a project that makes a real impact in healthcare



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