Quality Control Analyst II – Growth in Pharma QC Lab

Novo Nordisk A/S; Durham, Northern (NC, KY); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

14 paid holidays

Health insurance

Vision & dental insurance

401K with company match

Parental leave

Job summary

Novo Nordisk in Durham, NC is seeking a QC Analyst to perform and review analysis of in-process, release, and stability samples in accordance with cGMP and site procedures. Transfer of technology and processes will occur per project plans and timelines. You will report to the Senior Manager, QC – OFP.

The role emphasizes data integrity, GMP compliance, and collaboration with other analysts, with opportunities for professional growth within a global healthcare leader.

Qualifications

• Bachelor’s degree in Chemistry or relevant field required.
• Associate’s degree in chemistry with 3+ years of pharmaceutical lab experience.
• High School Diploma with 5+ years of clinical/industrial lab experience.
• Minimum of three years of experience in a clinical or industrial/pharmaceutical laboratory.
• Attention to detail required.

Responsibilities

• Accuracy & Scientific Soundness of Lab Data
• GMP Compliance of Laboratory
• Maintain testing proficiency for methods
• Timeliness of Lab Results & Investigations
• Analysis of Samples
• Author Deviations
• Coaching other analysts
• Data Trending & Tracking
• Ensure departmental documents are current & standardized
• Laboratory Equipment Validation & System support
• Laboratory IT System support
• Supports Deviations
• Systematic Problem Solving
• Follow all safety and environmental requirements in the performance of duties
• Other accountabilities, as assigned

Skills

Bachelor's degree in Chemistry

Attention to detail

Experience in clinical or industrial/药

Education

Bachelor's degree in Chemistry or relevant field

Associate’s degree in chemistry with 3 years experience

High School Diploma or GED with 5 years experience

Job description

Novo Nordisk in Durham, NC is seeking a QC Analyst to perform and review analysis of in-process, release, and stability samples in accordance with cGMP and site procedures. Transfer of technology and processes will occur per project plans and timelines. You will report to the Senior Manager, QC – OFP.

The role emphasizes data integrity, GMP compliance, and collaboration with other analysts, with opportunities for professional growth within a global healthcare leader.