About the Department
At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and 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 newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the-art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk's innovative oral products. At API, you'll join a global network of manufacturing professionals who are passionate about what they do.
What we offer you:
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance - effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 12 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
At 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 Position
Responsible for the production activities & validation. Ensures relevant compliance issues are addressed & handled in close collaboration with production. Main duties include review of batch reports & release of API materials, deviations, change controls, review & approval of SOPs, QA presence & process confirmation on shop floor & improvement of Quality processes.
Relationships
Reports to Manager, Quality Assurance.
Essential Functions
Ensure that the current Novo Nordisk (NN) procedures & requirements from health authorities are reflected in the validation planning & quality related decisionsSupport validation projects in communicating Novo Nordisk project quality requirements & assessing suppliers' ability to support test/qualification activities to ensure that Novo Nordisk requirements & expectations are clearSupport projects in solving quality related issues, act quickly in order to come to a decision, & communicate quickly & clearly regarding such decisionsSupport evaluation of the quality level during the project by performing spot checks of validation documentationPerform activities related to Batch review & releaseReview & approve API/Intermediate Batch documentation in various Novo Nordisk systems (e.g., LIMs, SAP, NovoGlow, etc.)Ensure site compliance with Regulations, ISO standards, & Corporate/Local SOPsReview & approve change control requestsReview & approve deviationsguidance to departments regarding quality & related activitiesParticipate & provide input to root-cause analysisParticipate in process confirmations & quality oversightAuthorized person according to Novo Nordisk Quality ManualOther accountabilities, as assignedPhysical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positionsAbility to do close precision work with their handsMust be able to remain in a stationary position (sitting and standing) 50% of the timeMay required corrected vision to 20/25 based on roleMay require color vision based on roleOccasionally ascends/descends a ladderMay be required to work at elevated heightsOccasionally works around odorous &/or hazardous materialsQualifications
BA/BS degree in Life Sciences, Engineering, or related field is requiredMinimum of five (5) years of experience within the pharmaceutical industry is requiredGood Knowledge of cGMP manufacturing & production processes & how to apply is requiredGood Knowledge of the Batch review Processes is requiredGood Knowledge of quality management systems is requiredGood Knowledge of quality oversight & on floor production support is required Strong knowledge level in cGMP's & validation is requiredStrong knowledge in Quality Management Systems is requiredMust be ability to perform tasks independently, accurately & within defined time frames is requiredAbility to willingly work with customers/stakeholders in a cooperative manner is requiredStrong written & verbal communication skills is requiredStrong computer skills in MS Office, PowerPoint, Word, Excel, etc. is requiredProven expertise in planning & organizing tasks preferredWillingness to assist others in developing plans in a cross-functional environment preferredInnovative approach to establishing priorities preferredLeadership: A high level of personal decision making in complex quality issues. Builds strong working relationships preferredParticipative/Supporting/Coaching: Actively participates in process/team activities, supports ideas/actions of others & provides solutions & feedback. Good communication skills preferredAgility: Robustness in handling of key stakeholders. Ability to prioritize changes in day-to-day environment & business needs preferredTeaming: Team player with strong communication skills preferredAppreciative: Demonstrates appreciative feedback style. Includes & recognizes other team members & their contributions preferredCustomer/Results Driven: Understands who the customer (internal/external) is, understands the customer's requirements, & understands the processes that generate products/services that meet the customer's requirements preferredFact Based Decision Making: Demonstrates a disciplined approach to problem solving that is based on data & facts, ensuring alignment with company goals & values preferredPersonally Accountable: Owns the results of their individual actions. Models the Novo Nordisk way preferredWe 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 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-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.