Senior IT Quality Professional

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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 [xxxxx] 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 78 highly skilled and ambitious quality professionals in Denmark and India. We are responsible for ensuring that external and internal requirements are reflected in [xxxxx] IT processes, and the department serves as competence center for IT quality assurance throughout [xxxxx]. 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.

    Working at [xxxxx] [xxxxx] is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at [xxxxx], we're working toward something bigger than ourselves, and it's a collective effort. Join us! Together, we go further. Together, we're life changing.

    Contact For further information, please contact department manager Sanaz Torab at [xxxxx]

    Deadline 21 March 2025. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At [xxxxx] 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 for 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 communities we operate in. Together, we’re life changing.


    Information og data

    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Ballerup.

    Jobbet er oprettet på vores service den 7.3.2025, men kan have været deaktiveret og genaktiveret igen.

    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • 17.03.2025
    • Øvrige
    • Ballerup

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