• Production Oversight and Compliance
• Supervise and manage the production of pharmaceutical products from raw material processing to final product packaging.
• Ensure that all production activities are in compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
• Review and approve batch records, manufacturing processes, and related documentation for accuracy and compliance.
• Maintain adherence to safety and environmental regulations in the production process.
• Quality Control and Assurance
• Implement quality control measures to ensure products meet all specifications and quality standards.
• Investigate deviations and non-conformances, and work closely with the Quality Assurance team to address issues and implement corrective actions.
• Conduct regular audits of the production area to ensure compliance with SOPs (Standard Operating Procedures), regulatory guidelines, and safety protocols.
• Process Optimization and Troubleshooting
• Monitor and analyze production processes to identify opportunities for process improvements and cost reductions.
• Work with engineering and technical teams to troubleshoot and resolve production issues, ensuring minimal downtime.
• Support the validation and qualification of new equipment and systems used in the production process.

Education:

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or a related field. A Master's or Doctorate degree in Pharmacy or a relevant specialty is a plus.
• Licensure:
• Must hold a valid pharmacist license (if required by local regulations).
• Must have minimum 5 years experience
• in manufacturing
• With knowleged in I.V. solutions
• Willing to work abroad

Skills:

• In-depth knowledge of pharmaceutical production processes and quality assurance procedures.
• Excellent communication, problem-solving, and analytical skills.
• Ability to work independently and in a team environment, managing multiple priorities and tasks effectively.
• Familiarity with computer systems and software used in pharmaceutical manufacturing (e.g., ERP, LIMS, MES systems).
• Personal Attributes:
• High attention to detail and a strong commitment to quality and regulatory compliance.
• Proactive, self-motivated, and capable of working under pressure in a fast-paced environment.
• Strong organizational and time management skills.