Position descriptionCategory:OPERATIONS - ENGINEERING/PRODUCTIONJob title:Project Engineer - C&Q Coordinator - PharmaContract:Permanent contractJob descriptionAkkodis 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 CoordinatorJoin 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 activitiesExecution: coordinate the resources performing the activity and/or department heads responsible for their teamsClosure of activities and related follow-upBusiness IndustryLife sciencesProfileEducation: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 sectorYou 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 youRequirements to start your growth path:Excellent level of English, at least B2 levelExcellent knowledge of the Microsoft Office Suite, Excel, and WordExcellent coordination skillsExcellent planning skills for complex activities involving numerous stakeholdersGood communication skillsOfferContract:PermanentLocation:FirenzeWhat is the added value of the Life Sciences division?Candidate criteriaMinimum level of education required:Master's DegreeLevel of experience:3 to 5 years#J-18808-Ljbffr
