نوو نور دیسک پارس

منتشر شده 6 سال پیش

Job Description

Would you enjoy working as Quality Assurance as well as Regulatory affairs? How about working in the QA team and ensuring products quality and compliance with authority requirements? Would you also enjoy being a part of ensuring that patients receive safe and high quality products? Then you might be our new Quality Assurance Regulatory affairs – grab this opportunity to write your own chapter in the Novo Nordisk success story and join us in making a difference for people around the world living with chronical diseases. In QA/RA 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, interacting with other Novo Nordisk sites. You will have the possibility of training sessions in Europe. You will work in our site which is approximately 60 Km vest of Tehran in the Barekat 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 the tone is relaxed, even if we are ambitious. You will be collaborating closely with your new team members, Novo Nordisk affiliate RA department and relevant authorities. You will be responsible for the site master file (SMF) preparation, ensuring SMF is always updated, participate in regulatory filing process as needed, in collaboration and ensure alignment with head quarter RA and affiliate RA. To ensure products and processes meet EU-GMP, Novo Nordisk A/S and local requirements. You will participate in review of change requests and non conformities, yearly evaluation of critical GXP suppliers. In your job you will cooperate with multiple stakeholders; processes owners, PS, IO and QAM head quarter I any issue impacting product quality patient safety and QMS compliance. You will be contributing to Quality Management Review and Product Quality Review In Novo Nordisk, you will be met with trust, interesting challenges and rich opportunity for personal and professional growth. You will be investing your unique skills in an environment focused around a competent sharing of knowledge, and where your talent and experience is valued. We are proud to use our dedication and our capabilities to make a difference for millions of people around the world.

Requirements

-Hold academic degree in Biology, Chemistry, Pharmacy or similar field. -At least 6 years of experience with relevant experience working with establishment of Device/Pharmaceutical manufacturing and/or manufacturing Pharmaceutical products is a must. Maybe you have already worked with development and optimization projects. -You will learn many new things here, but some of the areas we need you to already be quite experienced within: good knowledge on GMP pharmaceutical industry and on local requirement -Results-oriented such as being able to remain focused on site priorities and to maintain an effective balance between the short and long –term goals -Advanced in leadership such as leads by example and sets a good example for others -Understand and apply to the Novo Nordisk Way (NNW) in daily work •Being responsible, engaged with stakeholders, open and honest, including having the courage to bring forward own opinions and ideas, ready for change

Employment Type

  • Full Time

Details

Employment type

  • Full Time

Educations

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