About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
S4BT - Solutions for Business & Technology cerca un/una consulente per progetti di convalida di sistemi computerizzati in ambito chimico-farmaceutico. Si richiede laurea in discipline tecnico‑ingegneristiche e minimo 1 anno di esperienza CSV in Life Science.
Salary Range:€29,800.00 - €55,300.00 Job Description SummaryLocation: Ivrea, Italy #onsite Role Purpose: During the Pilot Plant ramp-up and operationalization, provide QA oversight and support for the establishment of a compliant quality system for GMP-relevant IT, OT, computerized, and
About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Job Purpose We are looking for a Junior Automation Engineer to support industrial automation activities across the companys pharmaceutical manufacturing sites, contributing to the maintenance, optimization, and development of plant control and supervisory systems while ensuring compliance
Pay Range (full-time): EUR 34.000 35.000 Professional | Permanent | Full-time | On-Site Our people in Manufacturing & Global Operations share two priorities: getting things done and making things better. If you’re a dynamic person with
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic
Process & Computer System Validation Specialist (GCP) Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti‑tumor therapies, is looking for a highly motivated and qualified Process &
Novartis Ivrea is seeking a QA Specialist to provide QA oversight for GMP-relevant IT/OT and computerized systems during ramp-up, focusing on system qualification, validation, data integrity, and lifecycle documentation. You will ensure compliant operation of IT/OT systems in manufacturing and labs,
About S.T.B. ValiTech Founded in 2004, S.T.B. ValiTech is a company in continuous expansion, with over 200 employees, specializing in equipment qualification, industrial calibration, Computer System Validation (CSV), Clean & Black Utilities, and electro‑instrumental design and installation. With
A leading biotech company in Italy is seeking a highly motivated Process & Computer System Validation Specialist (GCP) to join their QA department. The role involves validating computerized systems to ensure compliance with GMP/GCP regulations, contributing to data integrity in
Novartis in Ivrea, Italy is seeking a QA Specialist to support GMP-relevant IT/OT and computerized systems. The role focuses on qualification, validation, data integrity, and lifecycle documentation across manufacturing, QC labs, and utilities. Responsibilities include reviewing validation deliverables, ensuring proper
Validation Specialist (Data & Compliance) Italy - Onsite - Other - Other - Permanent contract We are hiring a CSV Specialist in Florence, Italy. Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities
Chi Siamo ProductLife Group (PLG) e una societa globale di consulenza e outsourcing nel settore delle Life Sciences che offre competenze specialistiche nelle aree di Sviluppo del Prodotto, Accesso al Mercato e al Paziente, Affari Regolatori,
Grünenthal Group in Lombardy (Origgio) seeks a dynamic professional for Manufacturing & Global Operations to support plant engineering, automation, and applications within a global, collaborative team. You will help implement the digital roadmap, apply engineering standards,
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose:
Make a meaningful impact on global healthcare — and grow your career while doing it. At ProductLife Group, you’ll join an innovative, forward‑thinking team operating across the world to shape the future of life sciences through
ProductLife Group is seeking an experienced CSV and validation professional to impact global healthcare. The role focuses on planning, executing, and coordinating Computerized System Validation activities for client projects in strict regulatory alignment with GAMP 5, GMP, Annex 11 and
Chi siamo ProductLife Group (PLG) è una società globale di consulenza e outsourcing nel settore delle Life Sciences che offre competenze specialistiche nelle aree di Sviluppo del Prodotto, Accesso al Mercato e al Paziente, Affari Regolatori,
The Equipment Specialist ensures the reliability, availability, and GMP compliance of the electronic, electrical, and automation systems installed on secondary packaging lines for ophthalmic products. The role is responsible for ensuring the proper operation of equipment and