Attiva gli avvisi di lavoro via e-mail!
Genera un CV personalizzato in pochi minuti
Ottieni un colloquio e una retribuzione più elevata. Scopri di più
ALTEN Italia recherche un Manager Technique pour rejoindre sa division Sciences de la Vie. Le candidat idéal aura au moins 10 ans d'expérience en CQV, capable de gérer des projets complexes et des interactions clients. En plus d'un salaire compétitif, des opportunités de développement de carrière et un environnement de travail collaboratif sont offerts.
ALTEN Italy , a leading force in the IT, Engineering and Life Sciences industries, is on the lookout for a vibrant and driven Techincal Unit Manager with a strong experience in CQV to join our dynamic team in the Life Sciences division. At ALTEN , we believe in the power of talent to drive innovation and success, and we're looking for an individual who shares our passion for connecting exceptional professionals with rewarding opportunities.
ALTEN Group
Within 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.
What are we looking for?
As a Technical Unit Manager with CQV expertise, you will play a key role in ensuring that pharmaceutical equipment, systems, and processes meet the highest standards of safety, reliability, and compliance. This role is ideal for a seasoned professional with a minimum of 10 years of experience in CQV who can independently manage complex projects and client interactions, especially during the bidding process.
Key Responsibilities :
Lead CQV projects from inception to completion, ensuring all deliverables meet regulatory and client expectations.
Oversee commissioning, qualification, and validation activities, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
Identify and mitigate risks associated with equipment, processes, and systems to ensure seamless project execution.
Collaborate with clients, project teams, and cross-functional stakeholders to ensure alignment and satisfaction.
Stay updated on industry trends, regulatory requirements, and best practices to provide cutting-edge solutions.
Qualifications :
What We Offer :
If you are passionate about quality, have a strong background in validation, and are looking for a challenging and rewarding opportunity, we will be waiting for you!