Managing Director – Life Sciences Consulting (Pharma CQV & Validation)

Key2people · Torino, Piemonte, Italia ·


Descrizione dell'offerta

Managing Director – Life Sciences Consulting (Pharma CQV & Validation)


A leading international consulting firm, specialized in regulatory compliance, qualification, and validation for the pharmaceutical, biotech, and cosmetics industries, is seeking a Managing Director to oversee its CQV business . The company is recognized for its technical expertise and integrated solutions, supporting clients in achieving the highest GMP standards across Europe, the US, and Asia.

Main Responsibilities

  • Full P&L responsibility for the CQV business, with a focus on leveraging existing know-how and driving growth in line with market trends and group synergies.
  • Implementation of the Business Development Plan, including organizational development.
  • Direct reporting to the Group BU Head and close collaboration with the CFO/Controller.
  • Guidance of service evolution and expansion, in coordination with technical teams and in line with established KPIs.
  • Contribution to sales, marketing, and business development, with direct management of client relationships and coordination with commercial teams.
  • Representation of the company at major industry organizations (AFI, ISPE, PDA), participation in conferences, and support for scientific publications.

Requirements

  • Master’s degree in Chemical/Industrial Engineering or a related scientific discipline.
  • Over 10 years of experience in the pharmaceutical sector, including at least 3-5 years in a managerial role within a consulting firm or life sciences business unit (CQV & Validation focus preferred).
  • Proven experience in P&L management.
  • Advanced English (minimum C1 level).
  • Strong leadership skills and experience managing diverse teams.
  • Established network and reputation in the pharmaceutical community, both in Italy and internationally.
  • In-depth knowledge of GMP (EU, US, international), commissioning & qualification, and process validation.
  • Experience with pharmaceutical manufacturing equipment, sterile production, clean utilities, HVAC/clean rooms, and computerized control systems.
  • Willingness to travel nationally and internationally.


Sede: Milano

RifMCP_55881

Candidatura e Ritorno (in fondo)