مدیر امور تنظیم مقررات

گروه دارویی داریان سلامت تهران

منتشر شده 4 روز پیش

Job Description

  • Interpret and implement quality assurance standards.
  • Evaluate the adequacy of quality assurance standards.
  • Document internal audits and other quality assurance activities.
  • Investigate customer complaints and non-conformance issues.
  • Develop, recommend, and monitor corrective and preventive actions.
  • Identify training needs and organize training interventions to meet quality standards.
  • Coordinate and support on-site audits conducted by external providers.
  • Evaluate audit findings (internal or external audits) and implement appropriate corrective actions.
  • Assure ongoing compliance with quality and industry regulatory requirements.
  • Analyze records of product returns to identify specific problems or trends over time.
  • Prepare documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, and corrective actions.
  • Prepare all quality department SOPs.
  • Ensure that manufacturing processes comply with GMP standards at both national and international levels.

Requirements:

  • Familiar with the laws and requirements of pharmacovigilance in pharmaceutical companies.
  • Proficient in the regulatory affairs of the Food and Drug Organization, preparing documents and files to send/register to the Ministry of Health.
  • Mastery of the Chargoon and TTAC systems for registering pharmaceutical products, supplements, and raw materials.
  • Proficiency in English
  • Doctor of Pharmacy.
  • At least 4 years of experience as a quality assurance manager in a pharmaceutical manufacturing company.
  • Leadership skills.
  • Problem-solving skills.
  • Communications and interpersonal skills.
  • Attention to detail.
  • Analytical thinking.
  • Maturity.
  • Result oriented.
  • Excellent documentation skills.
  • Fluent in English.
  • Excellent MS Office knowledge (Excel, Word, PowerPoint).
  • Good numerical skills and an understanding of statistics.
  • Familiar with local regulatory affairs and EU GMP standards.
  • Frequent traveling availability.

Employment Type

  • Full Time

Seniority

Details

Employment type

  • Full Time

Seniority

برای مشاهده‌ی شغل‌هایی که ارتباط بیشتری با حرفه‌ی شما دارد،

محاسبه‌کننده حقوق

چقدر حقوق بگیرم؟