We are looking for a "Production Manager (Non-Sterile)" with the requirements below:
Key Responsibilities:
Production & Quality
- Ensure manufacturing activities comply with cGMP, SOPs, and company standards.
- Detect, report, and resolve any issues affecting product quality.
- Oversee departmental SOP preparation, updates, training, and implementation.
- Support qualification, validation, and requalification processes of equipment and processes.
- Ensure cleanliness, order, and monitoring of production areas and equipment.
- Manage and track production consumables and procurement processes.
- Monitor work orders of completed products and provide necessary confirmations.
- Coordinate with internal departments for material and information flow.
- Support root cause analysis for customer complaints and deviations.
- Prepare the department for audits by local and international health authorities.
- Ensure CAPA (Corrective and Preventive Actions) are implemented and closed effectively.
- Conduct internal audits as assigned by the Quality Director.
Reporting & Administration
- Submit required reports accurately and on time.
- Monitor and respond promptly to internal communications (written or electronic).
Professional & Personal Development
- Stay updated on revisions in cGMP and Quality Assurance regulations.
- Follow global technological developments relevant to pharmaceutical production.
- Request additional training where needed and complete company-provided development programs.
Compliance & Ethics
- Perform all duties in compliance with GEN Caucasus internal regulations, disciplinary rules, and ethical standards.
- Use company resources (vehicles, IT equipment, mobile phones, etc.) responsibly.
- Ensure confidentiality of company information.
- Adhere strictly to working hours.
- Comply with occupational safety, health, and energy efficiency requirements.
- Work collaboratively with colleagues, managers, and other departments.
Energy & Environmental Responsibility
- Be aware of the energy impact of departmental activities.
- Follow operational instructions for energy-efficient practices.
- Record and report any deviations in energy performance parameters.
- Suggest improvements to enhance energy management and performance.
Additional requirements:
- Graduate of a University/associate degree
- Minimum of 8-10 years’ Industry experience (pharmaceutical or related)
- Minimum of 5 years’ experience in Management role
- Team player.
- Able to work under intense workload when necessary.
- Analytical thinking and problem solving
- Emotional agility and resilience
- Knowledge of sterile and non-sterile production processes
- Machinery and equipment expertise
- Planning, organization, and project management
- Crisis management and problem resolution
- Understanding of local and global pharmaceutical regulations
- Budget management and cost control
- Occupational health and safety practices
- Proficiency in MS Office programs
You are kindly asked to send your CV by indicating the position name in subject to the e-mail address in the Apply for job button.