Description

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 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 14 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

Support all daily activities of a cGMP warehouse operation including inspection, sampling, sample management, shelf-life expiry inventory, Job Instructions (JI) & regulatory compliance.

Relationships

Reports to Manager.

Essential Functions

• Package samples for transport
• Follow Standard Operating Procedures in performance of assigned duties
• Support GMP Laboratory and Environmental Compliance through daily tasks and ensure compliance with training programs related to job functions
• Partner with QC, QA, EM & support groups to ensure raw material release for production & resources to support schedules and enable the process to run optimally
• Maintain CNC areas & performing routine cleanings and batch turnover
• Complete all paperwork in a cGMP compliant manner
• Participate in Systematic Problem Solving, cLEAN Mindset, and streamlining processes
• Support validation & project activities as required
• Sampling of Raw Materials from Bulk tankers, Pressurized Containers, IBC's, drums & Palletized Material
• Ensure all errors are addressed & corrected real time ensuring compliance with cGMPs
• Record logbook entries & other associated forms/paperwork for the team
• Follow all safety & environmental requirements in the performance of duties
• Other duties as assigned

Physical Requirements

Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Ability to do close precision work with their hands. Strap & unstrap pallets using hands. Must be able to remain in a stationary position (sitting and standing) 50% of the time. May require corrected vision to 20/25 based on role. May require color vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. Handles transport of hazardous materials. Occasionally performs critical job functions in extremely cold work environments. Ability to work in loud noise environments with hearing protection. Able to pass a driving exam for powered industrial trucks. Does not require a valid drivers license.

Qualifications

• High School Diploma or equivalent with a minimum of one (1) year of experience operating in a GMP regulated environment required
• Associate's Degree in Science or relevant field of study from an accredited university preferred
• BioWorks Certification preferred
• Basic laboratory, sampling aseptic & ID testing techniques required
• Ability to read, write & understand product documentation & standard operating procedures with attention to detail & computer literacy required
• Knowledge of US, EU regulations & guidelines in reference to classified areas, sampling plans & methods & application of GMP's a plus
• Ability to communicate technical information clearly in writing & presentations preferred
• Demonstrated experience in practical problem solving & process improvements a plus
• Experience in LIMS system a plus
• Experience planning, organizing, executing, checking results & revising work plans a plus

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

We're not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

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.