Quality Control Analyst I - Precision Lab & GMP

Biopharma Careers; North Carolina; On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive pay and annual performance

Paid time off including holidays

Health, dental, and vision insurance (

401K with 8% company contribution

Parental & family leave

Tuition assistance

Life & disability insurance

Employee referral rewards

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, site and corporate procedures and policies. Transfer of technology and processes will occur in alignment with project plans and timelines.

Reports to Senior Manager, QC – OFP. This role emphasizes accuracy of lab data, environmental and GMP compliance, and maintaining testing proficiency while ensuring timely results and investigations in a

Qualifications

• Minimum of a Bachelor’s degree in chemistry or relevant field required or an equivalent combination of education and experience
• Associate’s degree with a minimum of three (3) years of experience in a clinical or industrial/pharmaceutical laboratory
• 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
• Must demonstrate attention to detail required

Responsibilities

• Accuracy and scientific soundness of lab data
• Environmental compliance
• GMP compliance of laboratory
• Maintain testing proficiency for methods
• Timeliness of lab results and investigations
• Analysis of samples
• Supports deviations
• Follow all safety and environmental requirements in the performance of duties

Skills

Attention to detail

Strong communication

GMP knowledge

Lab data analysis

Education

Bachelor’s degree in chemistry or related field

Associate’s degree in chemistry with 3+ years experience

High School Diploma or GED with 5+ years experience

Tools

UPLC

Dissolution

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, site and corporate procedures and policies. Transfer of technology and processes will occur in alignment with project plans and timelines.

Reports to Senior Manager, QC – OFP. This role emphasizes accuracy of lab data, environmental and GMP compliance, and maintaining testing proficiency while ensuring timely results and investigations in a