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Job Description

Are you highly motivated by being able to make a difference in improving patients’ lives? Are you a high-performing executive who is energized by taking exceptions and able to influence people around you? If so, you should continue reading and apply today.
At Novo Nordisk Pars in Kordan, the position of Quality Assurance Professional provides you the opportunity to work in a high-performing team and contribute directly towards the business results while creating value for diabetes patients.

About the department:

Novo Nordisk (NN) is a global healthcare company with 101 years of innovation and supervision in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat obesity, hemophilia, growth disorders, rare diseases, and other serious chronic diseases. Headquartered in Denmark, Novo Nordisk employs over 60,000 people in 80 countries and markets its products in more than 170 countries.
The LMT site is located in Barkat Pharmaceutical Industrial City, Alborz Province went into operation in 2020 and has 160 employees in total. The manufacturing site handles the assembly and packaging production of Novo Nordisk’s FlexPen® sold in Iran with modern insulin (NovoRapid®, NovoMix®30, Levemir®) and Victoza®.

The position:

As a Quality Assurance Professional (QA Professional), you will be responsible for ensuring products and business processes meet Good Manufacturing Practice (GMP), Novo Nordisk A/S, and local requirements.

Your main duties include, but are not limited to:

  • Ensure that all documentation related to manufacturing and quality control is accurate, complete, and in compliance with regulatory and corporate requirements. This includes SOPs, batch records, etc.
  • Handle and QA review of deviations and change control and cooperate in the audits, Quality Management Review (QMR), Quality Monitoring Trend (QMT), and Quality Risk Management (QRM) preparation.
  • Collaboration with processes owners, Production Support (PS), and Head Quarter in any issue impacting Product quality patient safety, and Quality Management System (QMS) compliance and handle other QMR training.
  • Accountable person for QA for qualification and validation and handle daily quality issues and review PPM Batch Control Record (BCR) NDA status assignments in SAP.
  • QA review and release of incoming material including cartridges and PPM and status assignment in SAP.
     

Requirements

  • Bachelor’s/master’s degree in Science-related disciplines (e.g. Life Sciences, Biology, Chemistry, Chemical Engineering, or Biotechnology).
  • At least 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 and have highly organized and detail-oriented mindset.
  • Upper intermediate level of English in both written and oral skills.

Working at Novo Nordisk:


We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research to our rich personal lives that motivate and energize us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.

Contact:
Please send your CV online and only in English (click on Apply and follow the instructions).

Deadline:
March 19, 2024;
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 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. Together, we’re life-changing.

Employment Type

  • Full Time

Details