QC Analyst III (3rd Shift)

WHAT WE'RE LOOKING FOR

We’re looking for a skilled and motivated  QC Analyst III  to join our Quality Control team. In this role, you’ll perform a variety of analytical tests to evaluate the quality of materials and products in a regulated pharmaceutical environment. You’ll work closely with formulation, filling, and packaging teams to ensure product integrity and compliance with regulatory standards. This position is ideal for someone who thrives in a fast-paced lab setting, values precision, and enjoys contributing to continuous improvement and audit readiness.

This position is based in Raleigh, NC, with an on-site, 3rd shift schedule of 9pm-5am. Overtime and alternate hours may be required during peak production periods.

YOUR ROLE

Perform wet chemistry tests and assays following SOPs and using laboratory instrumentation

Review and revise testing procedures, instrument protocols, and lab documentation

Support audit readiness and compliance with global regulatory standards

Conduct experimental work on future products and testing procedures under supervision

Record and report test results and significant observations accurately

Assist with special testing and validation of instruments and processes

Train new team members on lab procedures and compliance requirements

Collaborate with internal teams to support production and quality goals

Identify and report variations in test results, sample conditions, and equipment performance

Maintain a safe and organized lab environment in accordance with safety and environmental regulations

YOUR BACKGROUND

Education

Bachelor’s degree in Chemistry (preferred) or another science discipline with coursework in General, Organic, and Analytical Chemistry

Experience

2–3 years of analytical chemistry testing in an FDA-regulated environment (pharmaceutical manufacturing preferred)

Skills / Competencies

Ability to manage multiple tasks with accuracy and precision

Strong prioritization and leadership capabilities

Self-motivated, energetic, and team-oriented

Effective verbal and written communication skills

Proficiency in data analysis and computer-based lab systems

Knowledge of cGMPs, GLPs, FDA requirements, and laboratory safety standards

EQUAL EMPLOYMENT OPPORTUNITY

Guerbet is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant based on race, color, religion, national origin, sex, age, disability, veteran or military status, genetic information, pregnancy or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identity, and maintain employment statistics on applicants.

Applicants may be entitled to reasonable accommodation due to disability, pregnancy or related medical condition, or a sincerely held religious belief. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing an undue hardship on Guerbet. Please inform the company’s personnel representative if you need assistance completing this application or to otherwise participate in the application process.

Guerbet will not discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.

WHY GUERBET?

4 weeks of PTO

Insurance benefits start date of hire

Competitive 4% 401K match + 2% profit sharing contribution

Tuition reimbursement program for ongoing education

Paid time off for select volunteer opportunities