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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...CategorySelect how often (in days) to receive an alert:\xc3\x97Select how often (in days) to receive an alert:Senior Quality Professional I - Deviation and Change RequestCategory: QualityLocation:Bangalore, Karnataka, INDepartment: Operations Quality Consulting & ProjectsAre you an experienced quality professional looking for a new challenge? Do you thrive in a fast-paced and dynamic environment? We are seeking a Senior Quality Professional to join our team at Novo Nordisk. If you are passionate about ensuring compliance and driving quality excellence, then read on and apply today for a life-changing career.The PositionAs a Senior Quality Professional at Novo Nordisk, you will:Provide Compliance support for International Operations (IO) and North America Operations (NAO), focusing on Deviations, cold chain validation, and Change Request (CR) handling.Collaborate with OQCP/HQ specialists for timely support and follow-up on goals.Support setup and continuous improvement of Deviations, validation, and CR handling.Provide timely, specific, and quality support for Deviations, Qualification, and CRs.Assist in improvement projects, reporting to Management, and relevant tasks.QualificationsTo be successful in this role, we are looking for candidates with the following qualifications:University/equivalent degree (Pharmacy, Biology, Chemistry, Engineering or similar).Overall, 6-8 years of experience from the pharmaceutical industryAdept in handling DeviationsTrained and worked according to international validation principlesExperience with Change Request handlingExperience with GMP/GDP on operational levelIntercultural experienceAbout the departmentThe Senior Quality Professional position is part of the Operations Quality Consulting and Projects (OQCP) team. Based in Denmark, the OQCP team supports over 80 affiliates across Novo Nordisk with deviations, change controls, and qualification processes. As a member of the OQCP team, you will play a vital role in ensuring compliance and maintaining the Novo Nordisk Quality Management System in affiliates functions.Working at Novo NordiskNovo Nordisk 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 63,000 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 Novo Nordisk, 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.ContactIf you believe you are a match for the above requirements and are willing to take up the role, please apply here with our online application tool.DeadlineApply on or before: 29th April 2024We 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 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.

Novo Nordisk