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Novo Nordisk Quality Control Analyst I/II in Durham, North Carolina

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 -Solid Dosage Forms US 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. SDF 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 – 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

    Perform & review analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines.

    Relationships

    Senior Manager, Quality Control – OFP.

    Essential Functions

  • Accuracy & Scientific Soundness of Lab Data

  • Environmental Compliance

  • GMP Compliance of Laboratory

  • Maintain testing proficiency for methods

  • Timeliness of Lab Results & Investigations

  • Analysis of Samples

  • Supports Deviations

  • 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

  • Minimum of a Bachelor’s degree in chemistry or relevant field of study from an accredited university required or an equivalent combination of education and experience

  • May consider an Associate’s degree in chemistry or relevant field of study from an accredited university with a minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory

  • May consider a High School Diploma or GED with a minimum of five (5) years of experience in a clinical or industrial/pharmaceutical laboratory

  • Minimum of one (1) year of experience in a clinical or industrial/pharmaceutical laboratory required

  • Ability to author scientific & technical reports a plus

  • Able to perform routine testing per SOP & GMP standards a plus

  • Basic troubleshooting for laboratory equipment a plus

  • Knowledgeable in GMP & laboratory techniques a plus

  • Must demonstrate attention to detail required

  • Strong communication skills (verbal & written) a plus

  • Skills or knowledge in the following discipline: Chemistry Analysis of tablets including UPLC and Dissolution desired

    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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