Site Head

il y a 2 semaines

Bordeaux, Nouvelle-Aquitaine, France Irving Knight Group Temps plein

Job Title:
Site Head / Head of Operations / General Manager

Location:
Nouvelle-Aquitaine, France

Key Responsibilities:

Key Responsibilities:

  • Site Leadership:
    Provide strategic direction and hands-on management for all site operations, ensuring seamless integration of small and large molecule development and manufacturing services.
  • P&L Management:
    Full accountability for site P&L, including revenue growth, cost control, margin improvement, and achievement of financial targets.
  • Operational Excellence:
    Oversee daily operations, implementing best practices in cGMP manufacturing, process optimization, quality performance, safety, and regulatory compliance.
  • Talent Development:
    Lead, mentor, and develop a multidisciplinary team (approx. 140 people) to foster a high-performance, collaborative, compliant, and innovative culture.
  • Cross-Functional Coordination:
    Work closely with R&D, Quality, Supply Chain, Engineering, HR, and Finance teams to drive operational and business objectives.
  • Strategic Planning:
    Contribute to the organization's long-term strategy, identifying and implementing business growth initiatives, investments, and process improvements.
  • Regulatory Oversight:
    Ensure compliance with global regulatory requirements (FDA, EMA, etc.), and proactively manage inspections, audits, and quality initiatives.
  • Risk Management:
    Identify and mitigate risks to business continuity, compliance, financial performance, and reputation.
  • Reporting:
    Provide timely and accurate operational and financial reporting to executive leadership.

Qualifications:

  • Bachelor's degree in pharmacy, chemistry, biochemistry, chemical engineering, or related field; advanced degree (MSc, PhD, MBA) preferred.
  • Minimum 10 years' experience in pharmaceutical manufacturing with at least 5 years in a senior leadership role, ideally within a CDMO environment.
  • Demonstrated experience in managing both small and large molecule (biologics) operations. - Proven track record of successful site or business unit P&L management.
  • Deep understanding of cGMP, QA/QC, and global regulatory requirements for both small and large molecules.
  • Strong leadership, coaching, and team-building skills, with experience managing diverse technical teams.
  • Outstanding problem-solving skills and ability to drive continuous improvement.
  • Exceptional communication skills with fluency in English (written and verbal); other languages a plus.
  • Excellent organization, decision-making, and project management abilities.

Requirements:

  • Ability to work on-site in the South of France.
  • Proficiency in French and other European languages

Company:

  • Short of 1000 Employees
  • Global site network
  • Investing heavily across multiple sites

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