شرکت دارو سازی آتی فارمد در راستای تکمیل کادر خود از افراد واجد شرایط در تهران در ردیف شغلی زیر دعوت به همکاری می نماید.
متقاضیان محترم میتوانند رزومه خود را با ذکر ردیف شغلی مورد نظرخود به آدرس ایمیل زیر ارسال نمایند.
| Requirements | The Role | Job Title |
|---|---|---|
| - At least bachelor degree in human resource management - Experience: 5 years in HR fields - Fluent in Microsoft office (especially Excel and PowerPoint) - Good ability in English language - Inhabited in Tehran - Ideal Age: 30 - 40 - Male / Female | -Planning and maintaining personnel files in compliance with legal requirements - Manage all trends and regulations on HR such as: contracts, retention, attrition, productivity, disciplinary and compensation regulations - Manage and complete organization chart, job descriptions and occupational classification for all employees - Manage and direct recruitment department: interview and evaluate new employees, evaluate current employees and transfers - Manage and holding all training courses: external and in- house training and evaluate effectiveness of training courses - Keeping employee records up to date - Transportation services: Available from Tehran | Receptionist Travel Desk |
| - Education: Pharm .D - Majors: Chemistry, Industrial Engineering, Microbiology, Pharmacist - At least 3 years’ experience in Quality control - Fluent in English - Interested in job - Strong team work attitude - Self-control - Active listener | - Develops goals and plans for quality improvement. - Ensure the site QC processes align and support product specifications and specific customer requirements. - Responsible for ensuring good laboratory practices are implemented, documented, and sustained. - Responsible for non-conforming product process. - Identify critical points in the manufacturing process and specify sampling procedures to be used at these points. - Create and implement inspection and testing criteria or procedures. - Oversee workers including supervisors, inspectors, or laboratory workers engaged in testing activities. - Document testing procedures, methodologies, or criteria. - Review and update standard operating procedures or quality assurance manuals. - Review quality documentation necessary for regulatory submissions and inspections. - Direct all laboratory activities. - Devise ways of improving the manufacturing process to ensure higher-quality goods | Quality Control Manager |
این آگهی مربوط به ۲٬۹۰۷ روز پیش است و منقضی شده است بنابراین اطلاعات تماس نمایش داده نمیشود.
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