Responsibilities Ensure compliance of pharmaceutical products with GMP and regulatory standards. Perform document review and approval (batch records, SOPs, quality manuals). Conduct deviation analysis, CAPA implementation and monitoring. Support audits and regulatory inspections by preparing documentation
Join our team and start a new adventure in an international and dynamic environment, where you will be able to shape your professional ambitions in a fast‑growing organization. As an Amaris consultant, you will position yourself
Posted: 18.05.2026Job reference: 439a977702083aea55f32b0402453eb2Job informationLocationClient / EmployerAmaris ConsultingJob reference439a977702083aea55f32b0402453eb2Listing typeBasicEU work permit requiredNoPosted18.05.202602.07.2026Who are weAmaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe,