-Internal inspect according GMP requirements and provide analytical reports
-Gathering information to survey product quality
-Report, record and review deviations, preventive and corrective actions
-Record, check and confirm operational and in process Change
-Identify current risks and measure their severity
-Inspect suppliers and provide reports
-Academic degree in Biology, Chemistry, or similar field
-At least 2 years of relevant experience working in Pharmaceutical companies
-Have experience in Quality assurance (audit / Inspection, documentation, GMP compliance, ISO, familiar with Supplier qualification)
-The ideal candidate will need an open mindset who can work independently and as a team player with a strong focus on results, to succeed in this role
-Good communication skills with the ability to establish good relationship with local and global team
-Good or intermediate in English, both written and oral
-Ideal Age Range: 25 - 35
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Since 1994, CinnaGen Co. has invested her resources in production of molecular biology reagents and related technologies that would meet the highest international standards. With such efforts, we have established processes to meet all quality criteria. R&D plays an important role in our policies for advancement. Using our expertise, we are constantly moving towards new products as well as improving the quality of our existing product lines.
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