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CQV Manager (f​/m​/d

Job in 20093, Cologno Monzese, Lombardia, Italy
Listing for: Jacobs
Full Time position
Listed on 2026-08-16
Job specializations:
  • Engineering
    Operations Management, Regulatory Compliance Specialist
  • Management
    Operations Management, Project & Program Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 68600 EUR Yearly EUR 68600.00 YEAR
Job Description & How to Apply Below
Position: CQV Manager (f/m/d)
Location: Cologno Monzese

Job :
Cologno Monzese, All IT Regions, Italy Capabilities:
Chemical Office Setup:
Hybrid Salary: 68,600.Company:
Jacobs At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good.
Your impact
We are looking for an experienced Commissioning Manager with Qualification and Validation knowledge to lead our CQV department in Milan.

As CQV Manager, you will combine technical expertise, project leadership and people development. You will play a key role in delivering high-quality CQV projects for pharmaceutical clients while helping to grow and strengthen our team, capabilities, and ways of working across Italy and Europe.

This is an exciting opportunity for someone who enjoys working across different projects, collaborating with international teams and supporting the development of both people and the wider business.

Your impact

Reporting to the Milan Office General Manager, you will:
• Lead the successful delivery of Commissioning projects of biopharmaceutical facilities across Italy and Europe within the Milan office portfolio.
• Manage department resources, workload planning, and project priorities.
• Lead and support the growth of the CQV team, including recruitment, onboarding, training, mentoring, and career development.
• Coordinate the work of internal CQV engineers and external consultants.
• Identify suitable external consultants, manage their assignments, and oversee related contracts.
• Support local business development activities, including proposals, cost evaluations, and project team planning.
• Promote the harmonization and standardization of CQV procedures, knowledge, and best practice.
• Track project performance, progress, workload, and delivery risks.
• Organize and coordinate the weekly activities of CQV Engineers.
• Support continuous improvement across CQV delivery, aligned with current industry standards and client expectations.

You will provide leadership and technical direction throughout the CQV lifecycle, including:
• Managing commissioning activities from Mechanical Completion through Commissioning and Qualification to formal Systems Hand-over.
• Developing Commissioning and Qualification Master Plans, project strategies, procedures and protocols, including SAT, commissioning, IQ and OQ documentation.
• Reviewing technical documentation from the early design stages to ensure alignment with GMP and CQV requirements.
• Managing contractors and vendors and coordinating their activities on site.
• Investigating and resolving technical issues during the Commissioning and Qualification phases.
• Ensuring project execution follows company, department and client procedures, with a strong focus on health, safety and quality.
• Supporting the continuous improvement of CQV activities in line with GxP, ISPE and ASTM E2500 principles.
• Collaborating with clients, project teams and stakeholders across international locations.

The role involves approximately 50% travel across Italy and Europe. This provides the opportunity to work on a wide range of projects, build strong international relationships and broaden your professional experience.
Here's what you'll need

• A degree or equivalent qualification in engineering or a related discipline.
• At least 12 years’ experience in commissioning and qualification activities within pharmaceutical facilities.
• Previous experience leading or managing a CQV/C&Q team.
Project management experience, ideally across large and complex international projects.
• A solid understanding of GxP, ISPE and ASTM E2500 requirements.
• Experience developing CQV strategies, master plans, procedures and protocols.
• Experience managing contractors, vendors and multidisciplinary project teams.
• Proven commercial awareness, including project cost evaluation and resource planning.
• Fluency in Italian and English. German and/or French language skills would be an advantage.
• A collaborative and inclusive leadership style, with the…
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