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

Intermedia Selection; Lombardia; In loco; EUR 150.000 - 210.000; Tempo pieno

Vantaggi offerti da questo lavoro

Company car

MBO 20% bonus and benefits

Descrizione del lavoro

Intermedia Selection is seeking a Managing Director to oversee its CQV business within Life Sciences consulting. The role focuses on P&L ownership, strategic growth, and high-level client engagement across pharma, biotech, and cosmetics industries.

The candidate will guide service evolution, coordinate with technical teams, and represent the firm at major industry bodies (AFI, ISPE, PDA). Advanced English and a proven leadership track in pharma consulting are essential.

Competenze

• Master’s degree in Chemical/Industrial Engineering or related field.
• 10+ years in pharmaceutical sector with 3–5 years in a managerial role in a consulting firm or life sciences unit.
• Proven P&L management experience.
• Advanced English (C1).
• Strong leadership and diverse team management.

Mansioni

• Full P&L responsibility for the CQV business.
• Implement the Business Development Plan, including organizational development.
• Direct reporting to the Group BU Head and collaboration with CFO/Controller.
• Guidance of service evolution and expansion with KPIs.
• Contribution to sales, marketing and business development, with client relationship management.
• Representation of the company at AFI, ISPE, and PDA; support for publications.

Conoscenze

P&L management

Leadership

Team management

Advanced English

Formazione

Master's degree in Chemical/Industrial Eng or related

Descrizione del lavoro

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.

Remuneration Package:

• MBO equal to 20% of the GAS
• Company car and other benefits as per company policy