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Title

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Pharmaceutical Inspector

Description

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We are looking for a Pharmaceutical Inspector responsible for overseeing the regulation and compliance of pharmaceutical manufacturing, distribution, and usage. The goal of this position is to protect public health by ensuring the quality, safety, and efficacy of medicines. The Pharmaceutical Inspector works closely with pharmaceutical manufacturers, distributors, healthcare institutions, and regulatory authorities to ensure adherence to relevant laws and guidelines. Key duties include regular inspections of pharmaceutical manufacturing facilities, reviewing documentation, evaluating quality assurance systems, and reporting and sanctioning non-compliant practices. The inspector also participates in the approval process of new medicines, supervises clinical trials, and provides guidance on drug safety issues. The ideal candidate has strong knowledge of pharmaceutical regulations, GMP (Good Manufacturing Practice) standards, and is capable of working independently and in teams. Attention to detail, ethical conduct, and excellent communication skills are essential. This position is ideal for experienced pharmacists, quality assurance professionals, or individuals working in regulatory affairs who wish to contribute to the safe and effective operation of the pharmaceutical industry.

Responsibilities

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  • Inspect pharmaceutical manufacturing facilities
  • Review quality assurance systems
  • Ensure regulatory compliance
  • Support new drug approval processes
  • Supervise clinical trials
  • Analyze drug safety reports
  • Report non-compliant practices
  • Liaise with authorities and industry stakeholders
  • Check and approve documentation
  • Participate in audits and investigations

Requirements

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  • Pharmacy degree or related scientific qualification
  • Minimum 3 years of experience in the pharmaceutical or regulatory field
  • Knowledge of GMP and GxP standards
  • Strong communication and writing skills
  • Ethical and responsible work ethic
  • Analytical thinking
  • High level of precision
  • Ability to work in teams
  • English proficiency is an advantage
  • Flexibility and willingness to travel

Potential interview questions

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  • What experience do you have inspecting pharmaceutical facilities?
  • How do you ensure regulatory compliance in practice?
  • What quality assurance systems have you worked with?
  • Have you participated in drug approval processes?
  • How do you handle non-compliant practices?
  • What role have you played in supervising clinical trials?
  • What software or systems do you use for documentation management?
  • How do you communicate with regulatory authorities?
  • What challenges have you faced in drug safety?
  • What languages do you speak and at what level?