Entry-Level Quality Control Analyst – GMP Lab (Tablets)

Novo Nordisk A/S; Durham, Northern (NC, KY); Hybrid; USD 60,000 - 85,000; Full time

Benefits offered by this job

Competitive pay

Annual bonus

14 holidays

Health insurance day one

401K match

Parental leave

Tuition assistance

Life insurance

Disability insurance

Job summary

Novo Nordisk in Durham, NC, is seeking a Lab Analyst to perform and review analysis of in-process, release, and stability samples in compliance with cGMP and site procedures. Transfer of technology and processes will align with project plans and timelines.

The role reports to the Senior Manager, QC – OFP, and requires maintaining testing proficiency, timely results, and strict adherence to safety and environmental requirements. Strong attention to detail and communication are essential.

Qualifications

• Bachelor’s degree in chemistry or related field required; or equivalent education/experience.
• Associate’s degree in chemistry with 3+ years lab experience may be considered.
• High school diploma or GED with 5+ years laboratory experience may be considered.
• Minimum 1 year of laboratory experience required.
• Attention to detail is essential.

Responsibilities

• Accuracy & Scientific Soundness of Lab Data.
• 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.

Skills

Attention to detail

Strong communication skills

Teamwork

Quality & compliance mindset

Education

Bachelor's degree in chemistry or related field

Associate's degree in chemistry

High School Diploma or GED with 5+ years lab experience

Tools

UPLC system

Dissolution apparatus

Job description

Novo Nordisk in Durham, NC, is seeking a Lab Analyst to perform and review analysis of in-process, release, and stability samples in compliance with cGMP and site procedures. Transfer of technology and processes will align with project plans and timelines.

The role reports to the Senior Manager, QC – OFP, and requires maintaining testing proficiency, timely results, and strict adherence to safety and environmental requirements. Strong attention to detail and communication are essential.