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Quality Control Instrument Area Specialist
Quality Control Instrument Area Specialist-March 2024
Clayton
Mar 31, 2026
About Quality Control Instrument Area Specialist

  About the Department

  At Novo Nordisk, we want to make a difference. 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 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

  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

  Works closely with Laboratory personnel to support repairs, preventive maintenance & calibration of laboratory instrumentation. schedule resources as related to third party instrument services. responsible for activities related to BMS & alarm handling.

  Relationships

  Manager.

  Essential Functions

  Resource scheduling as related to third party instrument services

  Accurately & legibly records all activities in appropriate documentation. Writes work orders

  Reviews documentation for accuracy & completeness

  Instrument specifications, scheduled maintenance, repair, & calibration

  Identifies & handles deviations per proper procedures for measuring equipment

  Supports cross-functional investigations & participates in systematic problems solving

  Understand & execute GMP & compliance protocols for instrument validation

  Executes work according to schedule & department plan

  Evaluates instrument performance & responds to potential issues

  Contributes to process confirmations

  Maintains training qualifications on time. Supports training others as required

  Follow all safety and environmental requirements in the performance of duties

  Other accountabilities, as assigned

  Physical Requirements

  Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Ability to do close precision work with their hands. Must be able to remain in a stationary position (sitting and standing) 50% of the time. May required 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.

  Qualifications

  Bachelor’s degree in Chemistry, Engineering or a relevant field of study from an accredited university required

  May consider an Associate’s degree in Chemistry, Engineering or a relevant field of study from an accredited university with a minimum of seven (7) years of intense laboratory instrumentation experience in the pharmaceutical industry required

  Minimum of five (5) years of intense laboratory instrumentation experience in the pharmaceutical industry required

  Laboratory instrument calibration, maintenance & repair experience preferred

  Experience with LIMS & lab automation software, preferably Waters Empower preferred

  Extensive experience with MS Office products preferred

  Familiarity with SAP PM module and SAP QM module a plus

  High attention to detail preferred

  Excellent customer service skills preferred

  High level of organization in task management, as well as logical planning for task execution & follow-up required

  Systematic approach to problem solving & troubleshooting required

  Documents problems thoroughly & accurately & brings them rapidly to solution required

  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.

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