QC Analyst I: Launch Your Impact in GMP Lab

Initial Therapeutics, Inc.; Durham (NC); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

Paid holidays

Health insurance

401K match

Parental leave

Tuition assistance

Life & disability insurance

Employee referrals

Job summary

Novo Nordisk in Durham, NC invites applications for a QC Analyst role within the Emerging Technologies - Solid Dosage Forms facility. You will perform and review analysis of in-process, release, and stability samples in accordance with cGMP and site procedures.

Transfer technologies and support project timelines as required. The position reports to the Senior Manager, QC – OFP, and requires attention to detail, strong analytical skills, and GMP compliance.

Qualifications

• Bachelor’s degree in chemistry or related field required.
• Associate degree + 3 years pharma lab experience considered.
• HS diploma + 5 years pharma lab experience considered.

Responsibilities

• Ensure accuracy and scientific soundness of lab data.
• Ensure environmental and GMP compliance in the lab.
• Maintain testing proficiency for methods.
• Timely reporting of lab results and investigations.
• Analyze samples and support deviations.
• Follow safety and environmental requirements in duties.
• Perform transfer of technology and processes per plans.

Skills

Attention to detail

Analytical thinking

Scientific communication

GMP knowledge

Lab data integrity

Education

Bachelor’s degree in Chemistry or related field

Associate degree with 3 years lab experience

HS diploma with 5 years lab experience

Tools

UPLC

Dissolution

Job description

Novo Nordisk in Durham, NC invites applications for a QC Analyst role within the Emerging Technologies - Solid Dosage Forms facility. You will perform and review analysis of in-process, release, and stability samples in accordance with cGMP and site procedures.

Transfer technologies and support project timelines as required. The position reports to the Senior Manager, QC – OFP, and requires attention to detail, strong analytical skills, and GMP compliance.