تکنسین کنترل کیفیت

Job Description

Do you want to be part of our quality department and working in our Quality Control (QC) team? Grab this opportunity to write your own chapter in the Novo Nordisk success story, and join us in making a difference for people in Iran living with diabetes. In QC team we ensure products and business processes meet GMP, Novo Nordisk A/S and local requirements. You will be working in a young and dynamic team, with skilful and professional colleges. In this team we have a positive and friendly atmosphere; we are working in an international environment interaction with other Novo Nordisk sites. You will work in our site, approximately 60 Km vest of Tehran in Barkat Pharmaceutical town near the city of Karaj. Our collaborative mind-set is strong, and we enjoy sharing our knowledge, our challenges and our victories. We look forward to make you feel welcome, and you will soon find out that the tone is relaxed, even if we are ambitious. You will be collaborating closely with your new team members, ensuring products and business processes meet GMP, Novo Nordisk and local requirements. We also expected that you spend 40% of your working time on work with QC documentation, systems and 60% of your working time on practical work in the laboratory. We need you to perform practical activities during installation, qualification, calibration and maintenance all types pf lab equipment, assist QC professionals and QC chemists in implementation of on-going qualification, calibration and maintenance of OPC assembly lab equipment. We also need you to be familiar with analytical methods and practical performance of simple analytical methods in QC Lab such as Dose accuracy, Dose force, Extractable volume, Printed packaging material (PPM), Unintended Dose during regretting test (UDR Test), Participation in investigations and audits (Internal and External) in QC laboratory. familiar with QMS (SOPs, NCs, CRs, logbooks, protocols, OOS) to ensure compliance with QMS and GMP such as writing and keep SOPs updated relates to QC activities as content responsible. Registering OOS, participate in investigations of OOS resultant LI (lab investigation) and implement corrective actions when required. Involving in the archiving process in LMT, Logbook responsible, writing and keeping logbook updated in QC Lab. The position is rich in opportunities to gain expertise within Quality Control (QC) in an international pharmaceutical production company.