Advanced Pharmaceutical Industries Medina, Saudi Arabia

QA Qualified person

  • Medina
  • Advanced Pharmaceutical Industries Medina, Saudi Arabia
  • Posted date: 5 days before
  • End date: 2024-06-24

Job Title: QA Qualified person

Job In Medina

Company: Advanced Pharmaceutical Industries Medina, Saudi Arabia

Start Date: 2024-06-09

End Date: 2024-06-24




Job Description

As a QA Qualified person at our company, you will be responsible for ensuring the quality and compliance of our products and processes. You will work closely with cross-functional teams to develop and implement quality control measures and ensure that our products meet industry standards and customer expectations. The ideal candidate will have a strong attention to detail, excellent problem-solving skills, and the ability to work effectively in a fast-paced environment.

Responsibilities:

  1. Conduct quality inspections and audits to ensure compliance with regulatory requirements and industry standards.
  2. Develop and implement quality control measures to identify and address potential issues in product design, manufacturing, and packaging.
  3. Collaborate with cross-functional teams to define quality requirements and specifications for new products and processes.
  4. Review and analyze customer feedback and complaints to identify trends and areas for improvement.
  5. Lead investigations into quality issues and non-conformances to determine root causes and implement corrective actions.
  6. Monitor and evaluate the effectiveness of quality control systems and procedures, and make recommendations for improvements.
  7. Ensure that all documentation, including standard operating procedures, work instructions, and quality records, are accurate and up to date.
  8. Provide training and support to employees on quality assurance processes and procedures.
  9. Stay up to date with industry trends and developments in quality assurance practices.

Preferred Candidate:

  1. Bachelor's degree in a relevant field, such as Quality Assurance or Engineering.
  2. Minimum of 5 years of experience in a quality assurance role, preferably in the pharmaceutical or medical device industry.
  3. Strong knowledge of quality management systems and regulatory requirements, such as ISO 9001 and FDA regulations.
  4. Excellent analytical and problem-solving skills.
  5. Attention to detail and a high level of accuracy.
  6. Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  7. Ability to work independently and prioritize tasks in a fast-paced environment.
  8. Proficient in using quality assurance tools and software.
  9. Knowledge of statistical analysis techniques and tools is a plus.
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