Pharmaceutical Specialist

Employment Type:

Full-Time

• Oversee and manage the daily manufacturing operations of solid oral dosage forms, including tablets, capsules, and dry powders.

• Ensure all manufacturing activities comply with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and local regulatory requirements.

• Optimize production efficiency while maintaining the highest standards of product quality and safety.

• Oversee the complete manufacturing process, including raw material dispensing, granulation, blending, compression, coating, and capsule filling.

• Assist with the installation, qualification, validation, and calibration of production equipment.

• Monitor production schedules and ensure production targets are achieved efficiently.

• Support process improvements to maximize productivity and reduce downtime.

• Ensure strict adherence to cGMP standards throughout all manufacturing operations.

• Prepare, review, and maintain Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs).

• Develop, implement, and update Standard Operating Procedures (SOPs).

• Work closely with Quality Control (QC) and Quality Assurance (QA) teams to investigate deviations, OOS results, and production-related issues.

• Maintain complete and accurate production documentation.

• Troubleshoot manufacturing and formulation issues, including tablet capping, sticking, hardness variations, and dissolution concerns.

• Collaborate with analytical laboratories utilizing HPLC and FTIR instrumentation.

• Ensure in-process materials meet quality specifications before advancing to subsequent production stages.

• Support equipment validation and process optimization initiatives.

• Supervise, train, and mentor production technicians and operators.

• Promote compliance with safety procedures, hygiene standards, and GMP requirements.

• Maintain a clean, organized, and safe work environment in accordance with Environmental Health & Safety (EHS) standards.

• Foster a culture of continuous improvement and operational excellence.

• Bachelor's Degree in Pharmacy (B.Pharm) or Pharmaceutical Sciences.

• Master's Degree in Industrial Pharmacy or Pharmaceutics is preferred.

• Minimum 3–5 years of experience in pharmaceutical manufacturing, specifically within a Solid Dosage Forms facility.

• Experience supporting startup operations, facility expansions, equipment qualification, or validation projects is highly desirable.

• Strong knowledge of solid dosage manufacturing processes, including wet granulation, dry granulation, direct compression, and film coating.

• Understanding of cleanroom classifications, HVAC systems, and contamination control strategies.

• Thorough knowledge of international GMP standards, including WHO, EMA, or equivalent guidelines.

• Strong leadership and team management abilities.

• Excellent analytical and problem-solving skills.

• Exceptional attention to detail and documentation practices.

• Ability to perform effectively in a highly regulated environment and meet production timelines.
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  Languages

  • Fluent in Arabic.
  • WProficient in English, including pharmaceutical and technical terminology.
    If you m

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    et the qualifications and are interested in joining an innovative pharmaceutical manufacturing operation in Libya, we would love to hear from you.