Do you have a passion for working in a team of highly skilled IT Quality Assurance (IT QA) in a pharmaceutical IT setting? Do you have the desire to strive for the best quality in IT? Do you wish to be at the forefront of working with new digital technologies? Then you might be our next IT QA Professional. Apply now to join our company!
The position
Key responsibilities include:
Provide IT QA subject matter expertise (SME) in the GMP domain to projects/systems/services with focus on key quality activities and deliverables. Activities will range from advising on risk management, quality planning, approving quality related deliverables, to preparations for internal audits and external inspections by authorities.
Provide coaching and set direction for IT colleagues in quality and compliance tasks/issues.
Work closely with the agile project management teams and stakeholders in Line of Business (LoB). You are expected to leverage quality assurance, IT and business process knowledge (GMP), including IT technical expertise to ensure both efficient and effective quality assurance and compliance in an Agile setting.
The position offers a unique opportunity to work with IT Quality Management globally in Novo Nordisk and to develop you professionally through challenging job opportunities and formal training.
Qualifications
The position requires insight into quality processes like audit, deviation handling, validation, CAPA, change control, records management, data integrity, as well as insights into Good Manufacturing Practice (GMP), including solid working knowledge from within manufacturing and or working with infrastructure services for intended use Key IT processes, like Incident and Problem management, Configuration and Change management, Release and Deployment management, Testing and Validation (CSV), Operations management, Security and Risk management, etc. are implied.
We are especially looking for a candidate who can tick off most of the following:
BSc degree in Computer Science, Engineering, or another relevant field, preferably with a strong IT foundation
+5 years of work experience, as an IT QA in the pharmaceutical sector or years of experience as Production QA.
You thrive with stakeholder interaction, and you can present complex matters in a clear and precise way
You take full ownership for your work and have a strong sense for meeting objectives and delivering high quality
you have IT technical knowledge within regulated pharmaceutical sector and if you have worked in an agile setting
You are fluent in written and spoken English.
The department
IT QA Office is a part of IT Quality which employs around 70 highly skilled and ambitious quality professionals in Denmark and India. We are responsible for ensuring that external and internal requirements are reflected in Novo Nordisk IT processes, and the department serves as competence center for IT quality assurance throughout Novo Nordisk. Our responsibilities also include quality assurance of IT projects and IT systems, services and infrastructure used globally.
In IT QA Office we have highly motivated, engaged, and independent colleagues, an international environment where we share knowledge, experience, and where we help each other when needed.
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