QC Analyst II — cGMP, Data Trends & Impact
Novo Nordisk
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Benefits offered by this job
Job summary
Perform & review analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures and policies. Transfer of technology & processes per project plans & timelines.
Join Novo Nordisk's Durham, NC site, a 194,000 square foot tableting and packaging facility supporting our oral treatments. This role offers strong growth, competitive pay and comprehensive benefits.
Collaborate with Senior Manager, QC – OFP and mentors for professional development.
Qualifications
- Bachelor’s degree in Chemistry or related field required.
- Three years of experience in clinical or industrial/pharmaceutical laboratory.
- Attention to detail required.
- GMP knowledge and QC lab practices preferred.
Responsibilities
- Ensure accuracy and scientific soundness of lab data.
- Maintain testing proficiency for methods.
- Ensure GMP compliance of laboratory.
- Author deviations and support investigations.
- Coaching other analysts and data trending activities.
Skills
Education
Job description
Perform & review analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures and policies. Transfer of technology & processes per project plans & timelines.
Join Novo Nordisk's Durham, NC site, a 194,000 square foot tableting and packaging facility supporting our oral treatments. This role offers strong growth, competitive pay and comprehensive benefits.
Collaborate with Senior Manager, QC – OFP and mentors for professional development.
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