Manufacturing Process Technician I (Source) Job in North Carolina (NC), Career, Full Time Jobs in Novo Nordisk Inc.
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Life Science Career Fair

Manufacturing Process Technician I (Source) job in Clayton

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Novo Nordisk Inc. jobs
North Carolina (NC), Clayton
Job Code:  295172-en_US
Employer:  Novo Nordisk Inc.
Job Type:  Full Time

Location
Country:  United States
State:  North Carolina (NC)
City:  Clayton
03/28/2024

Description
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

Operate manufacturing equipment in order to achieve production goals.

Relationships

Reports to Shift Manager.

Essential Functions
  • Set up, operate, monitor & control equipment, systems & processes associated with production / manufacturing lines
  • Execution of production schedule to achieve production goals
  • Maintain production areas & perform cleaning
  • Actively participate in & support event response
  • Review & author SOP's & other documents, as required
  • Assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance
  • Train fellow employees in areas of expertise and actively learn systems & equipment outside of own area of expertise
  • Record/review production data in BPR's and associated forms
  • Follow all safety & 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. Routinely operates & inspects manufacturing equipment using hands. Ability to be on feet for up to a 12-hour shift. May required corrected vision to 20/25 based on role. May require color vision based on role. Ability to work in loud noise environments with hearing protection. Able to pass a driving exam for powered industrial trucks. Occasionally ascends/descends a ladder; work may be required at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. Occasionally performs job functions in cold work environment. Occasionally performs job functions within confined spaces for inspection, repair & maintenance of equipment.

Qualifications
  • High school diploma or equivalent required
  • Minimum of six (6) months manufacturing experience required
    • Minimum experience requirement may be waived with military experience, a BioWorks/BioBlend certification/equivalent from an accredited college, or a current Novo Nordisk contractor that has 3 months of demonstrated performance in the relevant area)
  • Experience working in an FDA regulated environment preferred
  • Production/Manufacturing experience preferred
  • Ability to read, write & understand product documentation & standard operating procedures with attention to detail required
  • Computer literacy preferred
  • Proven expertise in planning/organizing, managing execution, checking results & revising work plans a plus

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.
ref: (295172-en_US)
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