Pharmaceutical Engineer

2 weeks ago


Singapore Pharmeng Technology Pte. Ltd. Full time

Job Summary:

We are seeking a highly motivated and skilled Pharmaceutical Engineer to join our team. The successful candidate will play a pivotal role in the design, development, and manufacturing of pharmaceutical products. This position requires a deep understanding of pharmaceutical processes, regulatory compliance, and quality assurance. If you are a dedicated professional with a passion for ensuring the safety and efficacy of pharmaceutical products, we encourage you to apply.

Key Responsibilities:

  1. Drug Formulation: Collaborate with cross-functional teams to develop drug formulations, select suitable excipients, and optimize drug delivery systems.
  2. Process Development: Design, scale-up, and optimize pharmaceutical manufacturing processes to ensure efficiency, quality, and compliance with regulatory standards.
  3. Quality Control: Develop and implement quality control methods and protocols to monitor and ensure product quality throughout the manufacturing process.
  4. Regulatory Compliance: Stay up-to-date with pharmaceutical regulations (e.g., FDA, EMA) and ensure that all manufacturing processes and products adhere to relevant standards.
  5. GMP Adherence: Maintain adherence to Good Manufacturing Practices (GMP) and develop and update standard operating procedures (SOPs) as needed.
  6. Validation: Develop and execute validation protocols for manufacturing processes, equipment, and facilities to ensure consistent product quality.
  7. Research and Development: Participate in R&D activities, conduct experiments, analyze data, and contribute to the development of new drug compounds or dosage forms.
  8. Equipment and Facility Management: Select, install, and maintain pharmaceutical manufacturing equipment and facilities to ensure compliance with regulatory requirements.
  9. Documentation: Maintain accurate and comprehensive documentation of all processes, experiments, and validations for regulatory purposes.
  10. Collaboration: Work collaboratively with multidisciplinary teams, including chemists, pharmacists, regulatory affairs specialists, and quality control professionals.
  11. Continuous Improvement: Identify opportunities for process optimization, cost reduction, and quality enhancement, and implement improvements accordingly.

Qualifications:

  • Bachelor's or higher degree in pharmaceutical engineering or any engineering related field.
  • 5 years + of experience in pharmaceutical manufacturing or process development.
  • Strong knowledge of pharmaceutical regulations, including GMP and FDA guidelines.
  • Proficiency in data analysis and statistical tools.
  • Excellent communication and teamwork skills.
  • Detail-oriented with a commitment to quality and safety.
  • Problem-solving and critical thinking abilities.

Preferred Qualifications:

  • Bachelor's Degree in pharmaceutical engineering or any engineering related field.
  • Experience with regulatory submissions and interactions with regulatory agencies.
  • Knowledge of pharmaceutical equipment and facility design.
  • Familiarity with process simulation software.
  • Project management skills.

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