Quality Control Analyst I — GMP Lab & Impact

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

Benefits offered by this job

Leading pay & annual bonus

Paid time off & holidays

Health, dental, vision from day one

8% 401K match with company option

Parental & family leave

Job summary

Novo Nordisk’s Durham, NC facility is seeking a lab professional to perform and review analysis of in-process, release, and stability samples under cGMP procedures. This role involves transfer of technology and close adherence to project plans and timelines to support the injectable and oral product pipelines.

Ideal candidates hold a chemistry degree and have lab experience, with emphasis on method testing, environmental safety, and GMP compliance.

Qualifications

• Bachelor’s degree in chemistry or relevant field required or equivalent experience.
• Associate’s degree with 3+ years in clinical or industrial/pharmaceutical lab considered.
• High School Diploma with 5 years lab experience considered.

Responsibilities

• Perform and review analysis of in-process, release and stability samples.
• Transfer of technology and processes per project plans and timelines.
• Ensure GMP compliance and environmental safety in lab operations.
• Maintain testing proficiency for methods and timeliness of results.
• Support deviations and investigations as needed.

Skills

Attention to detail

Strong communication skills

GMP knowledge

Laboratory data integrity

Education

Bachelor’s degree in chemistry

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’s Durham, NC facility is seeking a lab professional to perform and review analysis of in-process, release, and stability samples under cGMP procedures. This role involves transfer of technology and close adherence to project plans and timelines to support the injectable and oral product pipelines.

Ideal candidates hold a chemistry degree and have lab experience, with emphasis on method testing, environmental safety, and GMP compliance.