نشان کن
کد آگهی: KP2244642348

At NanoAlvand, we are committed to upholding the highest standards of quality in everything we do. Our Quality Control department plays a vital role in ensuring that every product leaving our facilities meets regulatory requirements, national and international standards. We have implemented robust quality systems that govern every aspect of our operations, from raw material inspection to finished product release. Quality is more than just departments at NanoAlvand, it is a mindset that permeates our entire organization.OverviewAs a pharmacist in QC, you will be engaged in all quality related process through rigorous testing, analysis, and adherence to regulatory standards. In this position, you will collaborate closely with QC manager in all internal, domestic and international inspections for constant improvement of the department.Key ResponsibilitiesConducting analytical testing and inspections on raw materials, in-process samples, and finished drug products to verify they meet established quality standards.Utilizing and reviewing various analytical techniques and instrumentation, such as HPLC, FTIR, UV/Vis Spectroscopy, and others, to perform chemical analyses.Reviewing environmental monitoring results and reporting any out of limits results.Investigating and resolving any deviations, out-of-specification results, or quality issues that arise during the manufacturing and/or analysis process.Collaborating with other departments, such as production, QA, and R&D to ensure product quality and resolve quality-related issues.Participating in the development, implement, and improvement of analytical methods and testing procedures.Maintaining accurate and detailed records of all testing activities, results, and investigations in accordance with regulatory requirements.EducationDoctor of Pharmacy (Pharm.D)RequirmentsAge of 28-34Minimum 2 years of experience in pharmaceutical industryExtensive knowledge of current Good Manufacturing Practices (cGMP), international guidelines (e.g., FDA, EMA), and industry standardsStrong analytical and problem-solving skills, with the ability to interpret complex data and identify root causes of quality issuesExcellent written and verbal communication skills for documenting results and collaborating withcross-functional teamsAttention to detail and a commitment to ensuring the highest quality standards are met

نانو الوند
در کرج
در وبسایت ایران استخدام  (چند ساعت پیش)
اطلاعات شغل:
نوع همکاری:  تمام‌وقت
نیاز به سابقه:  حداقل 2 سال
ساعت کاری:  تمام وقت
متن کامل آگهی:

At NanoAlvand, we are committed to upholding the highest standards of quality in everything we do. Our Quality Control department plays a vital role in ensuring that every product leaving our facilities meets regulatory requirements, national and international standards. We have implemented robust quality systems that govern every aspect of our operations, from raw material inspection to finished product release. Quality is more than just departments at NanoAlvand, it is a mindset that permeates our entire organization.
Overview
As a pharmacist in QC, you will be engaged in all quality related process through rigorous testing, analysis, and adherence to regulatory standards. In this position, you will collaborate closely with QC manager in all internal, domestic and international inspections for constant improvement of the department.
Key Responsibilities
Conducting analytical testing and inspections on raw materials, in-process samples, and finished drug products to verify they meet established quality standards.
Utilizing and reviewing various analytical techniques and instrumentation, such as HPLC, FTIR, UV/Vis Spectroscopy, and others, to perform chemical analyses.
Reviewing environmental monitoring results and reporting any out of limits results.
Investigating and resolving any deviations, out-of-specification results, or quality issues that arise during the manufacturing and/or analysis process.
Collaborating with other departments, such as production, QA, and R&D to ensure product quality and resolve quality-related issues.
Participating in the development, implement, and improvement of analytical methods and testing procedures.
Maintaining accurate and detailed records of all testing activities, results, and investigations in accordance with regulatory requirements.
Education
Doctor of Pharmacy (Pharm.D)
Requirments
Age of 28-34
Minimum 2 years of experience in pharmaceutical industry
Extensive knowledge of current Good Manufacturing Practices (cGMP), international guidelines (e.g., FDA, EMA), and industry standards
Strong analytical and problem-solving skills, with the ability to interpret complex data and identify root causes of quality issues
Excellent written and verbal communication skills for documenting results and collaborating with
cross-functional teams
Attention to detail and a commitment to ensuring the highest quality standards are met

 

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گزارش مشکل آگهی
پنج‌شنبه 9 اسفند 1403، ساعت 16:02