Senior IT Quality Support Professional
Novo Nordisk A/S
Gladsaxe, 1 stilling
- Quality
- Denmark - Søborg
Are you passionate about good IT practices? Do you consider your skills as world class? Do you enjoy helping people ensure quality? Is your personality friendly, open-minded and robust? Read on, perhaps you are the new Senior IT Quality Support (ITQS) Professional we need.
About the department
The functional area, R&D Quality is built upon two departments, R&D QA and GCC (Global Clinical Compliance). R&D QA is responsible for quality assurance and provides quality and compliance support in pharmaceutical Research & Development (R&D). The department consists of three integrated teams: IT Quality Support team, RA (regulatory affairs) team and the QMS (quality management system) team. The vacancy is placed in the IT Quality Support team.
The team focuses on IT quality assurance and support in R&D, mainly for IT systems supporting Novo Nordisk clinical development (Global Development) and regulatory affairs (RA).
The job
As Senior ITQS Professional you will be responsible for quality assurance of one or more IT systems in R&D, provide quality support and compliance assistance to stakeholders in R&D. You will review and approve IT quality deliverables, change requests, standard procedures and nonconformities. You will also participate in IT projects, involving cooperation with stakeholders and global SAAS (Software-as-a-service) providers.
The IT Quality Support team works closely together with our colleagues in R&D Quality and across Novo Nordisk on GCP and GMP requirements, QMS requirements, input to global IT Procedures and IT quality issues in general.
Our stakeholders’ primary regulatory requirements are GCP, GMP and ISO9001 as defined in Novo Nordisk QMS. Our main stakeholders are located in Denmark and in Bangalore.
Qualifications
You hold a relevant scientific academic degree within Computer Science, Software Engineering or equivalent and are fluent in written and spoken English. The position requires significant insight into key IT processes: software engineering, quality management, change management, configuration management, risk assessment and testing.
Experience with teaching, project management, regulatory requirements (GCP/GMP), working in a quality function in the pharmaceutical industry and ISO9001 is an advantage.
You will cooperate with many other professionals and working cultures globally, which is why personal flexibility is a must. The job requires independence and the ability to continuously improve the quality mind-set within Novo Nordisk. You have a pragmatic approach to problem solving and strong interpersonal skills. You must be a team player prepared to work in a dynamic international environment with tight deadlines while maintaining a good sense of humour.
Do you want to join the team? We are looking forward to hear from you.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Anders Ravn Sørensen at +45 3075 4724 or Jakob Gade Grove at +45 3075 8646.
Deadline
13 Decmber 2015.
