Requirements: English
Company: ALTEN Italia
ALTEN Italy, a leading force in the IT, Engineeringand Life Sciences industries, is on the lookout for a vibrant anddriven Techincal Unit Manager with a strong experience in CQV tojoin our dynamic team in the Life Sciences division. At ALTEN, webelieve in the power of talent to drive innovation and success, andwe''re looking for an individual who shares our passion forconnecting exceptional professionals with rewarding opportunities.ALTEN Group Within 30 years, ALTEN has become leader in bothoutsourced Engineering and IT Enterprise Services. ALTEN, composedof 54,000 employees (88% engineers), carries out complex and highlytechnical projects throughout the value chain of 6,500 clients, themost prestigious companies in all sectors of industry, services andtelecommunications. We work with key actors in the Aeronautics& Space, Defense & Naval, Security, Automotive, Rail,Energy, Life Sciences, Finance, Retail, Telecommunications andServices sectors. What are we looking for? As a Technical UnitManager with CQV expertise, you will play a key role in ensuringthat pharmaceutical equipment, systems, and processes meet thehighest standards of safety, reliability, and compliance. This roleis ideal for a seasoned professional with a minimum of 10 years ofexperience in CQV who can independently manage complex projects andclient interactions, especially during the bidding process. KeyResponsibilities: - Project Leadership: Lead CQV projects frominception to completion, ensuring all deliverables meet regulatoryand client expectations. - Bid Management: - Analyze and interprettechnical requests from clients. - Identify risks and define keyassumptions. - Develop the best technical approach tailored toclient needs. - Define deliverables and estimate workloadeffectively. - Manage the bidding process autonomously, includingpresale activities and presenting proposals to clients. - TechnicalExpertise: Oversee commissioning, qualification, and validationactivities, ensuring compliance with Good Manufacturing Practices(GMP) and other relevant regulations. - Risk Assessment: Identifyand mitigate risks associated with equipment, processes, andsystems to ensure seamless project execution. - StakeholderEngagement: Collaborate with clients, project teams, andcross-functional stakeholders to ensure alignment and satisfaction.- Continuous Improvement: Stay updated on industry trends,regulatory requirements, and best practices to provide cutting-edgesolutions. Qualifications: - Minimum of 5 years of experience inCQV within the pharmaceutical or life sciences sector. - Provenexpertise in managing commissioning, qualification, and validationprojects independently. - Strong ability to manage bidsautonomously, including presales and client presentations. -Excellent analytical skills to understand technical requests,identify risks, and define project assumptions. - Deepunderstanding of regulatory requirements (e.g., GMP, FDA, EMA) andvalidation standards. - Exceptional communication and interpersonalskills to effectively engage with clients and stakeholders. -Bachelors or Masters degree in engineering, life sciences, or arelated field. - Native level of Italian and fluency in English isrequired. - Availability to visit clients within the perimeter.What We Offer: - Competitive salary based on experience. - Companycar as part of the benefits package. - Opportunities for careerdevelopment in a dynamic and growing international company. - Acollaborative and inclusive work environment. If you are passionateabout quality, have a strong background in validation, and arelooking for a challenging and rewarding opportunity, we will bewaiting for you!