Job Description

Job Description

Job Description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!

We are seeking a skilled Senior Quality Engineer to elevate our cell therapy manufacturing operations in our Springfield, MO location. In this impactful role, you will be the guardian of quality assurance, overseeing compliance with Good Manufacturing Practices (GMP), regulatory standards, and quality control processes.

QPS’ Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.

If this sounds like your ideal work environment, then we would love to speak with you, so apply today!

Please visit our website ( for more information and to see all current openings.

The Job

• Implement and enhance quality processes for cell therapy production to meet GMP, GCP, and regulatory standards.
• Collaborate with manufacturing teams to ensure compliant facilities, systems, and lab environments.
• Conduct audits, manage quality documentation, and lead CAPA initiatives to resolve deviations.
• Drive continuous improvement by developing and refining procedures, training programs, and compliance monitoring.

Work Location

• This job will be 100% QPS-office/facility based in our Springfield, MO location.

Requirements

• Manage audits and inspections for compliance and data integrity.
• Support equipment and process validation, ensuring robust manufacturing standards.
• Oversee SOP lifecycle management and employee compliance training.
• Prepare regulatory submissions and contribute to quality strategy for cell and gene therapy

Why You Should Apply

• Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
• Structured Career Ladders that provide excellent growth based on your personal aspirations.
• Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
• Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
• Park-like setting in Newark, Delaware
• Internal committees designed with the needs and enjoyment of QPS employees in mind.

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

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