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