Position description Category: OPERATIONS - ENGINEERING/PRODUCTION Job title: Project Engineer - C&Q Coordinator - Pharma Contract: Permanent contract Job description Akkodis is a global leader in the engineering and research and development market aiming to accelerate innovation and digital transformation using the power of connected data. With a passion for technology and talent, the group consisting of 50,000 engineers and digital experts offers deep cross-sector expertise in 30 countries across North America, EMEA, and APAC. The Lifesciences division of Akkodis is a leading Italian company in the field of engineering consultancy, validation, and GMP services for pharmaceutical, chemical, and healthcare companies. Composed of highly skilled technical consultants with proven experience in Good Manufacturing Practices, the company ensures full compliance with the quality requirements of the FDA and equivalent European bodies. Services include Engineering, Commissioning & Qualification, IT compliance, Process & Quality, Advanced therapies, GxP training. To strengthen our team, we are looking for a: Project Engineer - C&Q Coordinator Join our Life Sciences division, a group of around 400 consultants operating in Italy and about 3,000 in Europe in the Life Sciences sector across other European regions. Our strength lies in the integration of our skills, allowing us to have a 360° view of the pharmaceutical world. Your contribution at Akkodis: Within a team dedicated to Testing and Qualifications in the Pharmaceutical field, you will coordinate Qualification and Requalification activities throughout the year and during workload peaks. Each of these activities consists of three phases: Collection and consolidation of activities: coordinate the various functions performing the activities Execution: coordinate the resources performing the activity and/or department heads responsible for their teams Closure of activities and related follow-up Business Industry Life sciences Profile Education: Master's Degree in technical subjects, preferably in Engineering (Mechanical, Industrial, Chemical, Biomedical, Management, etc.) Experience: At least 3 years of experience in project management and C&Q activities in the pharmaceutical sector You will be able to join the Qualifications & Validations team of the Life Sciences division and work on an interesting project within a structured multinational company. About you Requirements to start your growth path: Excellent level of English, at least B2 level Excellent knowledge of the Microsoft Office Suite, Excel, and Word Excellent coordination skills Excellent planning skills for complex activities involving numerous stakeholders Good communication skills Offer Contract: Permanent Location: Firenze What is the added value of the Life Sciences division? Candidate criteria Minimum level of education required: Master's Degree Level of experience: 3 to 5 years #J-18808-Ljbffr
