Job Description

Do you have a strong desire to be part of a patient-centric company improving patient lives? Novo Nordisk Iran has opened a role for a quality assurance associate. Apply now and be part of Life-Changing Careers at Novo Nordisk. About Novo Nordisk: Novo Nordisk is a global healthcare company with more than 95 years of innovation and leadership in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat obesity, hemophilia, growth disorders, and other serious chronic diseases. The position As a quality assurance associate, you will be responsible for: ● Ensure products and business processes meet GMP, Novo Nordisk A/S, and local quality standards: ● Reception, reconciliation and QA review of Temperature traces drug product cold chain on time, informing relevant stakeholders about remaining time and assigning status to cartridge in SAP ● Issue Batch records, review assembly and repackaging Batch records including BPR and BCR, handle relevant tasks in SAP, and preparation of FP COA and RIMS report ● Review quality records in QDOCs or other paper base documents ● Review BCR for PPM and assign status in SAP ● Authorized QA by QP to perform QA sample examination and ensure QA sample compliance as per available procedures ● Compliance of LMT Quality Management System with NN Corporate requirements: ● QA review of change requests and QA review of deviations. ● Presence on shop floors and performing QA oversight. ● Cooperate in QMR, APR, and QMT preparation. Working at Novo Nordisk: At Novo Nordisk, we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company in the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to discuss flexible working, depending on the role and subject to business needs. Please send/upload your CV only in English. Due to the high volume of applications being received for this role, please note that only qualified candidates will be contacted. Millions rely on us: To work for Novo Nordisk you will need the skills, dedication, and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Requirements

● Bachelor’s or Master’s degree in science-relevant disciplines (e.g. Chemistry, Chemical Engineering, or Biotechnology). ● 2 to 3 years of quality assurance experience in the pharmaceutical industry; freshers are also encouraged to apply. ● Demonstrate knowledge of quality assurance and GMP compliance. ● Experience in reviewing batch records, quality control data, and regulatory inspections. ● Ability to manage multiple priorities with a deadline. ● Agility and intercultural skills. ● Highly organized and detail-oriented. ● Upper intermediate in English.

Employment Type

  • Full Time

Details

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