Quality Control Pharmacist

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.

Location
Simindasht Industrial Area, Karaj
Working Time
Full Time

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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