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Documentation Area Specialist III
3 months ago
About the Department
You will be joining Fill & Finish Expansions (FFEx), which is responsible for all major expansion activities within aseptic production, solid dosage forms, finished products, fill & finish warehousing, and QC across all production areas in Product Supply. The area is anchored in Product Supply, Quality & IT, which globally employ approx. 20,000 of Novo Nordisk's 50,000 employees.
FFEx is a newly established and growing area with the responsibility to design, plan, and build all new aseptic filling capacity across Novo Nordisk to serve the needs of millions of patients. We do it by rethinking our production facilities with the use of modern technology, as we are setting the standards for the aseptic production of the future. Facilities designed today which we will still be proud of 20 years from now. FF Expansions has a global approach, where you will be working with multiple sites and cultures across the world.
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
Designs, improves & maintains the document creation & revision process for various Novo Nordisk documentation. Key member of documentation control team who also serves as technical writing expert, incident investigator & SAP master data administrator. Supports training for lower-level peers.
Relationships
Manager.
Essential Functions
Provide specialist knowledge on the writing process to ease understanding, choice of document type, structure, style & language usage of the operational documentsServe as editor in NN documentation control process with focus on compliance that guarantees ease of use for document owners, users & quality approversCollaborate cross-functionally within siteProvide basic system administration leadership for end-user data processesSupport authors in the writing process with language usage, document control process & related softwareCoach document owners in the knowledge of good communication & standards in operational documentsSupport standardization projects as neededDevelop & maintain internal & external stakeholder relationshipsSupport project completion with metrics & timelines realizedProactively engaged in moderately complex systematic problem-solving activities collaborating on solutions regarding document processes & quality complianceServes as back-up to team lead for the Utilities organization to support deviation investigations as part of the site incident investigation processProficient in Change Control process to support revision of standardsAbility to support & act as a backup for the Site Expert/Super User for Quality DOCSProcess documents via applicable NN document management toolsFollow all safety and environmental requirements in the performance of dutiesOther 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). QualificationsAssociate's degree in Business or a technical field of study from an accredited university requiredMay consider a High School Diploma (GED) with seven (7) years of experience in technical writing or document processing required, preferably in engineering, life science or related industriesMinimum of five (5) years of experience in technical writing or document processing required, preferably in engineering, life sciences, or related industriesMinimum of three (3) years of experience with SAP preferredProven experience in GxP incident investigations and regulatory audit support preferredAbility to read, write & understand complicated product documentation & standard operating procedures with attention to high-level concepts preferredKnowledgeable in GMP concepts and SAP preferredKnowledge of process improvement methodologies such as LEAN preferredStrong communication and organizational skills preferredHighly proficient in the following software applications/tools: MS Word 2010, Adobe Acrobat Pro (latest version), Excel, PowerPoint, & Visio requiredProven expertise in planning, organizing, managing, executing, & revising the work plan & schedules for complex problems solved by cross functional teams requiredDemonstrated strong skills in change management within NN 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 This contact is for accommodation requests only and cannot be used to inquire about the status of applications.