Job Information
Novo Nordisk Senior Quality Assurance Area Specialist (Automation) in Clayton, North Carolina
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; d esign & develop quality & compliance set-up for the Automation process during the project. Monitor Automation work package for relevant quality related issues. Ensure compliant execution & monitoring. Drive corrective actions & quality improvement initiatives within Automation work package.
Relationships
Manager, Quality Assurance.
Essential Functions
Ensure that the current NN procedures & requirements from health authorities are reflected in the validation planning & quality related decisions
Support 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 clear
Support projects in solving quality related issues, act quickly in order to come to a decision, & communicate quickly & clearly regarding such decisions
Support evaluation of the quality level during the project by performing spot checks of validation documentation
Perform activities related to Batch review & release
Review & 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 SOPs
Review & approve change control requests
Review & approve deviations
guidance to departments regarding quality & related activities
Participate & provide input to root-cause analysis
Participate in process confirmations & quality oversight
Authorized person according to Novo Nordisk Quality Manual
Other accountabilities, as assigned
Physical Requirements
May move equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. May be required to be on your feet for up to a 12-hour shift. May required corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. May require the ability to work in loud noise environments with hearing protections.
Qualifications
Bachelor's Degree in Life Sciences, Engineering, or related field required
Minimum of five (5) years of experience within the pharmaceutical industry required
Good Knowledge of cGMP manufacturing & production processes & how to apply required
Good Knowledge of the Batch review Processes required
Good Knowledge of quality management systems required
Good Knowledge of quality oversight & on floor production support required
Strong knowledge level in cGMP’s & validation required
Strong knowledge in Quality Management Systems required
Must be ability to perform tasks independently, accurately & within defined time frames required
Ability to willingly work with customers/stakeholders in a cooperative manner required
Strong written & verbal communication skills required
Strong computer skills in MS Office, PowerPoint, Word, Excel, etc required
Proven expertise in planning & organizing tasks preferred
Willingness to assist others in developing plans in a cross-functional environment preferred
Innovative approach to establishing priorities preferred
We 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 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.