Production Director

2 settimane fa

Milano, Lombardia, Italia Hartmann Young A tempo pieno 60.000 € - 120.000 € all'ano

Job Description: ( Apply only if relevant )

Position:
Production Director (Steriles facility)

Reports to:
Site Head

Key Responsibilities

Operations Management

  • Manage production, inspection, and packaging departments to meet defined targets and GMP standards.
  • Plan and coordinate production activities in line with sales forecasts and budget objectives.
  • Ensure supply of materials, efficient resource allocation, and optimal staffing and training.
  • Collaborate with Quality, Supply Chain, Engineering, and Commercial teams to meet production timelines and maintain service levels.
  • Oversee introduction of new products and ensure operational continuity of facilities and equipment.
  • Drive continuous improvement and efficiency initiatives through performance monitoring (KPIs) and cross-functional projects.
  • Manage operational and investment budgets, proposing cost-effective and strategic improvements.
  • Maintain hygiene, safety, and compliance across all production areas.
  • Lead regular operational reviews and support GMP and client inspections.

People & Development

  • Ensure proper training, qualification, and GMP knowledge of all personnel.
  • Support career development, performance evaluation, and incentive recommendations in line with HR policies.
  • Promote teamwork, safety culture, and adherence to company values.

Health, Safety & Environment

  • Ensure compliance with environmental, health, and safety regulations (Legislative Decree 81/08).
  • Implement and monitor safe work procedures, risk assessments, and emergency measures.
  • Supervise adherence to PPE use, safety protocols, and environmental protection standards.
  • Report deviations and coordinate with SHE and HR functions for corrective actions.
  • Ensure contractors and suppliers comply with site safety and environmental requirements.

Compliance & Governance

  • Adhere to the Organisation, Management, and Control Model (Legislative Decree 231/01).
  • Cooperate with the Supervisory Body and ensure proper reporting and procedural compliance.

Skills & Knowledge

  • Qualification
    • Degree in Pharmaceutical Chemistry and Technology, Pharmacy, Biology/Engineering, preferably with professional certification and registration with the relevant Professional Association
  • Experience in the role and/or in Production/QA departments Knowledge and Skills
  • Minimum of 3-5 years CDMO manufacturing experience, in Sterile & LIO environment
  • Excellent knowledge of English
  • Business acumen and budgeting techniques
  • Knowledge of environmental and safety management system principles
  • Understanding of risks and environmental aspects present in the facility
  • Knowledge of health, safety, and environmental regulations

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