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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