Job description

Key Responsibilities

Technical & Manufacturing Assessment

Pharmaceutical Production

Laboratory & Facility Development

Regulatory & Quality Compliance

Qualifications

Experience

• Evaluate opportunities for manufacturing synthetic pharmaceutical products in Bahrain.
• Identify suitable products for local and regional markets.
• Assess production processes, equipment requirements, and facility specifications.
• Recommend manufacturing technologies and operational models.
• Provide technical expertise in the formulation and production of synthetic medicines.
• Develop and optimize manufacturing processes.
• Support technology transfer and scale-up activities.
• Establish production workflows and batch manufacturing procedures.
• Define laboratory and production facility requirements.
• Recommend equipment, utilities, and infrastructure specifications.
• Support facility design and commissioning activities.
• Ensure compliance with GMP and pharmaceutical manufacturing standards.
• Assess regulatory requirements for pharmaceutical manufacturing in Bahrain and GCC markets.
• Support licensing and regulatory approval processes.
• Establish quality control and quality assurance frameworks.
• Bachelor's or Master's Degree in Pharmaceutical Sciences, Industrial Pharmacy, Chemistry, Medicinal Chemistry, or a related field.
• Additional GMP, Quality Assurance, or Pharmaceutical Manufacturing certifications preferred.

Skills

• Minimum 10 years of experience in pharmaceutical manufacturing.
• Demonstrated experience in the production of synthetic medicines.
• Strong knowledge of pharmaceutical manufacturing processes, formulation development, and GMP requirements.
• Experience in setting up or expanding pharmaceutical production facilities is highly desirable.
• Knowledge of GCC pharmaceutical regulations is preferred.