Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines,
We offer an interesting opportunity to join our Quality Operations team, based in Bussolengo (VR) as Quality Control Engineer , reporting to the Supplier Quality Engineer Supervisor, on a full-time permanent contract. As part of the Quality
Job SummaryTVS SCS RICO Italia is part of a multinational company specialized in providing a wide range of technological services throughout Europe, including Break & Fix, IMAC, Service Desk, Projects and Rollouts, Help Desk, End User
Job Description SummaryThe Global Process Engineer (GPE) will work closely with the Global Manufacturing Engineering Leader, the primary focus area will be developing and deploying global standards that improve the reliability, availability, and performance of Aero
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered
Join Saipem and engineer a sustainable future. We are a global leader in engineering and construction for the energy and infrastructure sectors, delivering complex onshore and offshore projects worldwide. Driven by technological innovation as “One Company”,
Quality Engineer Location: Eindhoven region (Netherlands) Employment Type: Full-time Contract Type: Long-term (with potential for permanent employment) Relocation support available About the Role Are you a Quality Engineer with experience in high-tech manufacturing environments ? We are
Quality Engineer Location: Eindhoven region (Netherlands) Employment Type: Full-time Contract Type: Long-term (with potential for permanent employment) Relocation support available About the Role Are you a Quality Engineer with experience in high-tech manufacturing environments ? We are
Failure Analysis Engineer Location: Netherlands (relocation support available) Industry: Semiconductors / Electronics / Mechatronics Employment Type: Full-time Contract Type: Long-term (1–2 year contract, with potential for direct hire by client) About the Role Are you an Electrical or
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice
Are you a high-performing software architect who has already made the shift to AI-first development, directing coding agents rather than writing code yourself? Do you want to work for a best-in-class, 100% remote organization with the
We offer an interesting opportunity to join our Quality Operations team, based in Bussolengo (VR) as Quality Control Engineer , reporting to the Supplier Quality Engineer Supervisor, on a full-time permanent contract. As part of the Quality
Plant Cleaning, Sanitization & Pest Control Referent Job Location: ALBA About the role: We are currently looking for a Plant Cleaning, Sanitation & Pest Control Referent for our Plant in Alba. As Cleaning, Sanitation and Pest
Job Summary This is an opportunity for an industry-recognized pharmaceutical polymer materials subject matter expert (SME) to serve as the technical authority on polymer-based primary packaging components for Lillys parenteral drug products - including elastomeric closures
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine
Olin is a global chemical company and a leading producer of chlor‑alkali products, epoxy resins and chlorinated hydrocarbons. Founded in North America in 1892, Olin today employs more than 7,800 people in more than 15 countries.
We’re Nadara. We work harmoniously with the power of nature and the communities around us to power lifetimes to come. We call our approach ‘living energy’. We don’t just produce renewable energy, we live it –
Expert OverviewIn this role, you will plan and conduct independent clinical (GCP) audits across IQVIA contracts to verify regulatory and guideline compliance. You will produce and share findings with stakeholders, and advise project teams on interpretation of
Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines,
Why join the Manufacturing department? Our mission in the Manufacturing department is to deliver high-quality products efficiently and sustainably while driving innovation across our production processes. We operate in a safe and environmentally conscious environment, supported