Quality Control Analyst I - SDF

Novo Nordisk•Durham, NC

1d•Onsite

About The Position

Novo Nordisk is a global healthcare company with over 100 years of experience in tackling unmet medical needs for people with serious chronic diseases like diabetes and obesity. The 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 innovative oral treatments for type 2 diabetes patients. This facility fosters a curious and pioneering spirit, aligning with the company's growing pipeline of new products and emerging technologies. Novo Nordisk offers competitive pay, annual performance bonuses, generous paid time off, comprehensive health benefits effective day one, a guaranteed 8% 401K contribution with a company match option, and extensive family-focused benefits including paid parental and family medical leave. Additionally, employees receive free access to Novo Nordisk-marketed pharmaceutical products, tuition assistance, life & disability insurance, and employee referral awards. The company provides opportunities, resources, and mentorship for career growth.

Requirements

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
Minimum of one (1) year of experience in a clinical or industrial/pharmaceutical laboratory required
Must demonstrate attention to detail required
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 colour vision based on role.
Occasionally ascends/descends a ladder.
May be required to work at elevated heights.
Occasionally works around odorous &/or hazardous materials.

Nice To Haves

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
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
Strong communication skills (verbal & written) a plus
Skills or knowledge in the following discipline: Chemistry Analysis of tablets including UPLC and Dissolution desired

Responsibilities

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.
Maintain testing proficiency for methods.
Support Deviations.
Follow all safety and environmental requirements in the performance of duties.