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
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
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 &
About usChiesi 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
Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements. Prepare, review, and manage
Specific activities and responsibilities:Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements.Prepare, review, and manage validation documentation, including
Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements. Prepare, review, and manage
Productlife Group seeks an experienced CSV validation professional in Italy to plan, coordinate, and execute computerized system validation for client projects, ensuring compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11. You will manage validation documentation,
Are you passionate about the Internet of Things and eager to make a significant impactinthe digital engineering landscape? We are seeking a dynamicIIoT Associate Engineer to become a vital part of our clients forward-thinking Digital Engineering
Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.Join our global team dedicated to innovation and initiative, where physical
Job PurposeThe R&D Digital Solutions Specialist supports the operation, compliance and continuous evolution of digital systems that enable efficient, high quality clinical development across the Group.Working closely with the Group R&D Digital Solutions Manager, the role combines
Company Description In over 37 years, Eurofins has grown from a single laboratory in Nantes, France, with more than 65,000 employees in a decentralized and entrepreneurial network of over 950 laboratories in more than 1,000 companies
About Philogen Philogen S.p.A. is a biotechnology company dedicated to developing targeted products for the imaging and treatment of life-threatening diseases, with a strategic focus on oncology. Our mission is to translate cutting-edge scientific innovation into
CSA & Quality Compliance Expert with 3-5 years of experience in Computer System Validation to support compliance and validation projects for our clients, including top pharmaceutical, biotech, and medical device companies.Role DescriptionThe selected candidate will work as a consultant
Company Description In over 37 years, Eurofins has grown from a single laboratory in Nantes, France, with more than 65,000 employees in a decentralized and entrepreneurial network of over 950 laboratories in more than 1,000 companies
Company DescriptionIn over 37 years, Eurofins has grown from a single laboratory in Nantes, France, with more than 65,000 employees in a decentralized and entrepreneurial network of over 950 laboratories in more than 1,000 companies across
Company Description In over 37 years, Eurofins has grown from a single laboratory in Nantes, France, with more than 65,000 employees in a decentralized and entrepreneurial network of over 950 laboratories in more than 1,000 companies
Purpose The Automation Lead reporting to the Engineering & Maintenance Site Manager, is responsible for leading the technological evolution of automation systems for the Group affiliates within the Global Manufacturing Division (GMD) perimeter. In the Operational Technology
Job Title: Metrology ManagerLocation: Verna , GoaAbout the JobAt Sanofi, we are committed to supporting a healthier future by delivering high-quality medicines and vaccines to patients around the world.The Goa Site Engineering & Maintenance (E&M) team
Stiamo selezionando un o una Scada Engineer per una realtà specializzata nello sviluppo di soluzioni di automazione industriale dedicate ai processi produttivi del settore farmaceutico (water facilities, bioreattori, sistemi di purificazione, impianti di processo). Esperienza, qualifiche