Novo Nordisk Quality Assurance Area Specialist I or II in Clayton, North Carolina
About the Department
At Novo Nordisk, we want to make a difference. For nearly 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 legacy Injectable Finished Products (IFP) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At IFP, 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 – reimbursement up to $10,000 annually
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.
Ensures Batch Production Records (BPRs) & relevant quality processes are compliant with regulations. Release of raw materials. Quality oversight, review & approval of validation activities associated with minor changes to existing systems. Prepare periodic system evaluations for maintaining validated state. Quality review & approval of Change Requests (CR’s), Deviations & other documentation. Performs Self Audits (in conjunction with LoB), QA presence & process confirmation on shop floor.
Note: This position is D shift, nights, 6:00 PM to 6:30 AM, 3-2-2 rotation.
Ensures site compliance with Regulations, ISO standards, corporate & local SOPs
Reviews & approves documentation for Quality approval – components/raw material, batch records, change control requests, deviations & validation documents
Participates in project teams as a quality resource
Supports, reviews & approves investigations & root-cause analysis
Participates in process confirmations & Go Look Sees
Evaluates trend & report data for QMRs & APR reports
Other duties, as assigned
BA/BS degree in life sciences or related field, or an equivalent combination of education & experience.
Minimum of 4 years of QA and/or quality related experience in the pharmaceutical or medical device industry with progressively increasing responsibility
General knowledge of regulations & quality systems (e.g. product disposition, NC/CAPA, Change Control, Audits, Supplier Management, Project Management, etc.)
Familiarity with local processes & quality systems
Demonstrated knowledge of critical controls & input/output requirements for NNPILP processes
Knowledge of Quality, Aseptic Production, Business Support, QC, O&P and/or Finished Production processes
Knowledge of US, EU regulations & guidelines, ISO standards & application of GMPs in aseptic manufacturing
Excellent written & verbal communication skills
Basic computer skills in MS Office, MS Project, PowerPoint, etc.
Auditing experience with certification preferred
Experience in the use of Six Sigma & LEAN tools
Personal Time Management: Sets goals & prioritizes tasks for own work on short-term basis. Meets deadlines & makes regular progress reports on performance. Keeps track & informs management about fluctuation in workload. Performs well with multi-tasking. Adjust priorities in accordance with changing circumstances. Keeps all relevant people informed of current & future plans
Physical & Other Requirements
Occasionally moves equipment and/or supplies weighing up to 33 pounds within the facility using various body positions
Able to work in an open office environment with the possibility of frequent distraction
Able to work the hours necessary to support a 24/7 continuous manufacturing operation
Able to adjust schedule to work with colleagues in other international time zones
Some roles require ability to work 12 hour shifts or longer, day or night
Able to travel domestically and/or internationally, as necessary
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.
Novo Nordisk requires all new hires to be fully vaccinated against COVID-19 prior to the first date of employment. As required by applicable law, Novo Nordisk will consider requests for reasonable accommodation.
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.
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