Job Description

About the Department For 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 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 Emerging Technologies - Oral Finished Products 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. OFP maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.
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 \xe2\x80\x93 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 \xe2\x80\x93 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.
The Position Support the implementation of science & risk-based validation. The incumbent will provide input to project team members through all stages of specification setting, supplier selection, & commissioning/qualification/verification. Perform revalidation on equipment/processes per approved timelines. Support validation activities associated with changes to existing & new systems. The incumbent will help develop requirements, build/construct, design, commission & perform SAT, FAT & verification activities for projects according to science & risk-based validation (SRV).
Relationships Reports to Manager, Process Support \xe2\x80\x93 OFP.
Essential Functions

• Partner with the Sr. Validation Area Specialist to participate in & provide feedback to international corporate validation process group
• Ability to work & communicate effectively across multiple local departments. multiple international production sites
• Perform & review system, equipment, utility, & process revalidation per corporate science & risk-based validation principles
• Support the collaboration, writing, executing, & review of IQs, OQs, PQs, & other verification protocols for systems/processes
• Support the creation & review of documentation (Specifications, SOPs, etc.) in accordance with local, corporate & regulatory regulations
• Support &/or lead the closure of investigations per approved timeframes using root cause analysis & systematic problem-solving techniques
• Participate in teams to help identify root causes of failures & implement corrective actions which address & eliminate potential reoccurrence of the failures
• Support the development of new processes & product flows
• Understand processes & products
• Support Global OFP sites with investigations & issues, to include on-site support
• Evaluate results of process confirmations of standards for opportunities to leverage & share ideas for improvements site/division/company wide
• Track & assess effectiveness of corrective / preventative actions from audits, inspections & investigations
• Participate in continuous improvement initiatives using cLEAN tools & methodology
• Ensure executed protocol data reviewed is accurate & meets documented acceptance criteria
• Support change control efforts for process improvements & identify opportunities for improvements
• Responsible for Change Requests (CR\xe2\x80\x99s) related to revalidation & other validation activities
• Support validation concepts & approaches for audits & inspections
• Author & review validation procedures, specifications & quality documents for accuracy & compliance
• Present & support validation concepts & approaches for audits & inspections
• Follow all safety & environmental requirements in the performance of duties
• Operate in alignment with NNWay, demonstrating a Quality & cLEAN\xc2\xae Mindset
• Provide oversight & administration for the training program
• Other accountabilities, as assigned

Physical Requirements Ability 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.)
Qualifications

• BA/BS degree from an accredited university in engineering or related technical field required. May consider Associate Degree from an accredited university in engineering or related technical field with 2 years of relevant experience or a High School Diploma or GED with 4 years of relevant experience
• The following experiences are preferred:
  • Minimum of two (2) years of validation- related discipline experience in pharmaceutical or medical device industry
  • Experience in quality concepts including technical & compliance review of validation & quality documents
  • Experience in one or more core validation areas (equipment, cleaning, process, or computer validation)
  • Exp\xc3\xa9rience in cGMP documentation practices & r\xc3\xa9gulations
  • Basic computer skills including experience in the use of Microsoft Word, Excel, etc.
  • Strong oral & written communication skills
  • Experience in project team collaboration & support
  • Demonstrated expertise in planning/organizing, managing execution, checking results & revising the work plan for complex problems being resolved by cross functional teams

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\xe2\x80\x99re 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.