3rd-Shift QC Analyst: Chemistry & Compliance

NCBiotech; Raleigh (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Disability accommodations

Job summary

Guerbet is seeking a QC Analyst to join our chemistry lab on a 3rd shift, evaluating material and product quality through wet chemistry tests and collaborating with formulation, filling, and packaging teams. This role requires attention to SOPs, regulatory adherence, and accurate documentation.

You will help maintain an audit-ready status for FDA and other global regulators, perform experimental work on future products, and train new staff.

Qualifications

• Bachelor’s degree in chemistry (preferred) or related science.
• 2–3 years of analytical chemistry testing in an FDA-regulated environment (pharmaceutical manufacturing preferred).

Responsibilities

• Perform wet chemistry tests and assays per standard operating procedures and instrumentation.
• Review and revise existing testing procedures, instrument procedures, and laboratory documentation procedures as needed.
• Assist in providing laboratory with an audit-ready status for regulatory agencies.
• Perform experimental work under supervision on future products and testing procedures.
• Record and report results and significant observations.
• Perform special testing and assist in instrument and process validations when directed.
• Assist in training new team members on testing procedures and compliance regulations.
• Work in a team environment to support internal and external customer requirements.
• Perform other duties as assigned by management.

Skills

Analytical Chemistry

Teamwork

Time management

Leadership

Communication

Education

Bachelor’s degree in chemistry

Job description

Guerbet is seeking a QC Analyst to join our chemistry lab on a 3rd shift, evaluating material and product quality through wet chemistry tests and collaborating with formulation, filling, and packaging teams. This role requires attention to SOPs, regulatory adherence, and accurate documentation.

You will help maintain an audit-ready status for FDA and other global regulators, perform experimental work on future products, and train new staff.