Lavoro Major - Ivrea

Summary -Shift Lead I -The Shift Leader is responsible for managing his team to carry out the manufacturing operations according to schedule in compliance with HSE and GMP rules. -Process Specialist / Equipment Specialist -Execute assigned manufacturing tasks and activities according to production s...

Location: Ivrea, Italy Role Purpose: Design, plan and perform Mass Spectrometry experiments as well as report and interpret results/outcome in line with the overall TRD RLT (Radioligand Therapy) project strategy for RLT Drug Substance(s) and Drug Product(s) in development. Ensure project knowledge g...

Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, contributes to operation...

Summary Guarantee the operation in compliance of all the pharmaceutical and general equipment and systems present in Saluggia site (intended GMP compliance, Normative and Standard compliance, eCompliance) in order to satisfy necessary requirements of pharmaceutical processes and safety requirements,...

Permanent JobWho are we?Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international tea...

Permanent Job Who are we? Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international t...

Responsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process perfor...