QC Analyst II - cGMP Data & Deviation Expert
Initial Therapeutics, Inc.
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Benefits offered by this job
Job summary
Novo Nordisk in Durham, NC is seeking a Quality Control Analyst to perform and review analysis of in-process, release and stability samples in accordance with cGMP and site procedures. You will support transfer of technology and processes per project plans, reporting to the Senior Manager, QC – OFP.
Required: a chemistry-related degree with minimum three years of pharma lab experience and strong attention to detail; GMP knowledge is a plus.
Qualifications
- Bachelor's degree in Chemistry or related field required.
- Associate's degree with 3+ years in pharma lab considered.
- High School Diploma with 5+ years in clinical/industrial pharma lab considered.
- At least 3 years of clinical or industrial/pharmaceutical lab experience.
- Attention to detail required.
Responsibilities
- Perform and review analysis of in-process, release and stability samples per cGMP.
- Transfer of technology and processes per project plans and timelines.
- Report to Senior Manager, QC – OFP.
- Author deviations and participate in investigations.
- Maintain testing proficiency and lab data integrity.
Skills
Education
Job description
Novo Nordisk in Durham, NC is seeking a Quality Control Analyst to perform and review analysis of in-process, release and stability samples in accordance with cGMP and site procedures. You will support transfer of technology and processes per project plans, reporting to the Senior Manager, QC – OFP.
Required: a chemistry-related degree with minimum three years of pharma lab experience and strong attention to detail; GMP knowledge is a plus.
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