WHAT WE'RE LOOKING FOR We’re seeking a highly motivated and detail-oriented  Sr. QA Engineer – Validation Specialist  to lead and support validation activities across equipment, utilities, and computer systems in a pharmaceutical manufacturing environment. This role is essential to ensuring compliance with cGMP, GLP, and FDA regulations while driving continuous improvement and operational excellence. You’ll collaborate with cross-functional teams, provide technical guidance, and take ownership of validation deliverables from planning through execution.

This is an on-site position located in Raleigh, NC. YOUR ROLE Author, execute, and summarize validation protocols for equipment, utilities, and computer systems

Coordinate and manage validation projects, ensuring timely and compliant execution

Develop and revise procedures to align with cGMP, GLP, and FDA regulations

Provide technical input on new equipment and modifications to maintain validated status

Support investigations related to critical equipment, processes, and utilities

Train personnel on validation procedures and compliance standards

Recommend policy and procedural changes to enhance regulatory compliance

Notify management of deviations and recommend corrective actions for out-of-spec systems

Conduct special projects and provide technical support as directed by management

Maintain a safe working environment and report safety or environmental concerns promptly YOUR BACKGROUND

Education Bachelor’s degree in Engineering, Life Sciences, or equivalent validation experience Experience 2–6 years of validation experience in a pharmaceutical manufacturing environment Skills/Competencies Strong knowledge of cGMP, GLP, and FDA regulations

Experience with pharmaceutical equipment, cleaning validation, and steam sterilization

Proficiency in writing protocols, reports, and technical documentation

Ability to apply advanced mathematical and statistical principles

Skilled in problem-solving, data analysis, and drawing valid conclusions

Proficient in MS Office (Word, Excel, PowerPoint, Access) and database tools

Effective communicator with strong technical writing and interpersonal skills

Self-motivated, organized, and capable of managing multiple priorities

Demonstrated accountability and ability to meet deadlines with high accuracy 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