Validation Area Specialist I/II - SDF

About The DepartmentFor more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.What We Offer YouLeading pay and annual performance bonus for all positionsAll employees enjoy generous paid time off including 14 paid holidaysHealth Insurance, Dental Insurance, Vision Insurance – effective day oneGuaranteed 8% 401K contribution plus individual company match optionFamily Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leaveFree access to Novo Nordisk-marketed pharmaceutical productsTuition AssistanceLife & Disability InsuranceEmployee Referral AwardsAt Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.The PositionPlan, manage & perform low to moderately complex validation projects and activities. Support engineers with writing change requests and conducting/writing deviation investigations. Support validation activities associated with changes to existing & new systems as assigned. Process equipment supported includes propagation, fermenters, media sterilizers and the related supporting equipment. Collaborate & coordinate with IT, Metrology & other key stakeholders to ensure quality, cost effectiveness in alignment with budget targets & timely completion of all deliverables.RelationshipsReports to Manager, Director.Essential FunctionsPerform, review & approve validation/revalidation. Must be able to work & communicate effectively across multiple departments to schedule & perform validation/revalidation assignmentsReview & approve documents in accordance with local, corporate & regulatory regulationsCollaborate, review & approve protocols for systems/processes per approved timeframesParticipate in teams to help identify root causes of failures & implement corrective actions which address & eliminate potential reoccurrence of the failures, to include supporting investigation closure per approved timeframes using root cause analysis techniquesEnsure executed protocol data reviewed is accurate & meets documented acceptance criteriaResponsible for Change Requests (CR’s) related to revalidation & other validation activities as assignedReview & approve validation procedures, specifications & quality documents for accuracy & complianceProvide support for validation concepts & approaches with audits & inspections as assignedSupport change control process and identify opportunities for improvementsAuthor & review validation procedures, specifications & quality documents for accuracy & complianceOperate in alignment with NNWay, demonstrating a Quality & cLEAN® MindsetFollow all safety & environmental requirements in the performance of dutiesOther duties as assignedPhysical RequirementsAbility to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time. (% can change on a case-by-case basis based on the role.)QualificationsBachelor’s degree in engineering, pharmaceutical sciences or related field of study from an accredited university required and a minimum of two (2) years of validation related discipline experience in pharmaceutical or medical device industry required In lieu of BS degree + two (2) years of experience, may consider an Associate’s Degree in engineering, pharmaceutical sciences or related field of study from an accredited college or university required with a minimum of four (4) years of relevant validation experience in pharmaceutical or medical device industry requiredIn lieu of BS degree with two (2) years of experience, may consider a High School Diploma or equivalent required with a minimum of six (6) years of relevant validation experience in pharmaceutical or medical device industry requiredExperience in quality concepts including technical & compliance review of validation & quality documents preferredExperience in one or more core validation areas (equipment, sterilization, cleaning, process clean & black utilities or computer validation) preferredExperience in cGMP documentation practices & regulations preferredBasic computer skills including experience in the use of Microsoft word, Excel, etc preferredKnowledge of statistical methods preferredStrong oral & written communication skills preferredExperience with validation test equipment including temperature mapping equipment (for example: Ellab Validator), desired preferredExperience working with cross functional teams preferredBeginning knowledge of problem-solving using root-cause analysis techniques to solve problems preferredDemonstrated expertise in planning/organizing, managing execution, checking results & revising the work plan for complex problems being resolved by cross functional teams a plusWe commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.