Job Description
Are you passionate about ensuring the highest quality standards in pharmaceutical products? Do you have a keen eye for detail and a commitment to excellence? If so, we invite you to join our Quality Control team at Novo Nordisk. At Novo Nordisk Pars in Kordan, the position of Quality Control Professional provides you the opportunity to work in a high performing team and contribute directly towards the business results while creating values for the diabetes patients. Read more and apply today for a life-changing
About the department:
Novo Nordisk (NN) is a global healthcare company with over 100 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 About the department
The LMT site is located in Barkat Pharmaceutical Industrial City, Alborz Province and 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®.
You will join the Quality department at LMT, where we define and specify activities, processes, and standards to fulfil the quality requirements for services or manufactured materials, components, or products. Our activities include auditing, monitoring, and finding the quality of processes or outputs against defined internal or regulatory standards. We report on process deviations and defects, identify and develop outsourcing vendors and suppliers according to organizational quality standards and policies, and resolve vendor/supplier problems related to quality, performance, quantity, timing, etc. Our team is committed to ensuring the highest quality standards and continuously improving our processes.
The position:
As a quality control professional, you will ensure products and business processes meet Good Manufacturing Practice (GMP), Novo Nordisk Automated Storage (A/S) and local requirements, and QC documentation whilst performing practical analyses.
- Perform practical activities during installation, qualification, calibration, and maintenance of lab equipment and supervise simple equipment-related processes.
- Be responsible for the validation of all QC equipment and metrology, oversee simple analytical methods, and create/update analytical procedures (Standard Operating Procedures (SOPs).
- Create verification protocols/reports for analytical methods, ensure compliance with Quality Management System (QMS) and GMP, and write and keep updated SOPs related to QC activities.
- Perform actions on non-conformities (NCs) / Change Requests (CRs), register Out of Storage (OOS), participate in investigations of OOS results, and act as System Manager of QC IT solutions.
- Train, develop, and direct technicians within key areas of responsibility, maintain a clean and orderly working place and follow business ethics principles and quality system rules.
Requirements:
- Master's degree in Engineering with 4 years of relevant experience in Device/Pharmaceutical manufacturing or pharmaceutical products establishment.
- Knowledge of pharmaceutical quality and regulatory requirements, business understanding of pharmaceutical product production, and good knowledge of GMP Pharmaceutical Industry and local requirements.
- Strong IT capability and results-oriented with a balance between short- and long-term goals.
- Leadership qualities, effective teamwork skills, and intercultural competence, with agility and flexibility to adapt to new conditions.
- Strong organizational skills, commitment to quality, and continuous improvement, while understanding and embodying the principles of the Novo Nordisk Way (NNW).
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:
Upload your CV to our online career page (click on Apply and follow the instructions).
Deadline:
3 December 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.
