QC Analyst I – GMP Lab & Data Quality

BioSpace; Durham (NC); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance

401K Match

Paid holidays

Parental leave

Tuition Assistance

Job summary

Novo Nordisk in Durham, NC is seeking a Laboratory Analyst to perform and review analysis of in-process, release, and stability samples. You will ensure adherence to cGMP and site procedures, and assist with technology transfer in line with project plans and timelines.

The role emphasizes accurate data, environmental safety, and timely reporting of results. Qualified candidates will have a chemistry background and lab experience in pharma settings, with strong communication and documentation

Qualifications

• Minimum bachelor’s degree in chemistry or related field or equivalent experience.
• Additional associate or high school level with required laboratory experience considered.
• Experience in clinical or industrial/pharmaceutical lab environments preferred.

Responsibilities

• Perform and review analysis of in-process, release and stability samples.
• Ensure compliance with cGMP, site and corporate procedures.
• Transfer of technology and processes per project plans and timelines.
• Maintain testing proficiency and timeliness of lab results.
• Support deviations and safety/environmental requirements.
• Collaborate with QA and manufacturing teams as needed.

Skills

Attention to detail

Scientific data integrity

Communication skills

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

Tools

UPLC

Dissolution testing

Job description

Novo Nordisk in Durham, NC is seeking a Laboratory Analyst to perform and review analysis of in-process, release, and stability samples. You will ensure adherence to cGMP and site procedures, and assist with technology transfer in line with project plans and timelines.

The role emphasizes accurate data, environmental safety, and timely reporting of results. Qualified candidates will have a chemistry background and lab experience in pharma settings, with strong communication and documentation