Quality Control Specialist I

Geneoscopy; Maryland Heights (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Vision insurance

Dental insurance

Life insurance

401k (employer match)

Paid time off

Stock options

Job summary

Geneoscopy is seeking a Quality Control Specialist I in St. Louis, MO to perform QC reviews of sample data, ensure data integrity, and support compliance with CLIA, CAP, NYS, DOH, FDA, ISO, and other standards.

The role collaborates with lab, manufacturing and quality teams to drive continuous improvement. The ideal candidate holds a Bachelor's in a science field, has 1–2 years in a regulated environment, and is capable of reading procedures, multitasking, and communicating effectively in a

Qualifications

• Bachelor's degree in a science-related field (prefer Biology or Chemistry).
• 1–2 years of experience in a CLIA/CAP or QSR-regulated environment.
• Minimum of 2 years of PCR testing experience.
• Ability to read and understand technical procedures and instructions.
• Multitask effectively in a fast-paced, deadline-driven environment.

Responsibilities

• Conduct QC reviews of sample/specimen data for accuracy throughout the testing process.
• Evaluate incoming materials and inspect components/products at various stages.
• Support data and manual entry QC checks for laboratory and clinical operations.
• Update or open nonconformances for inaccurate data in collaboration with laboratory personnel.
• Track and trend QC data and prepare quality presentations.
• Assist in maintaining compliance with CLIA, CAP, NYS, DOH, FDA, ISO, and related regulations.

Skills

Quality control

Data review

Regulatory awareness

Procedural reading

Communication

Team collaboration

Education

Bachelor's degree in science

Biology or Chemistry

Job description

Quality Control Specialist I

This is an onsite, in-office position at Geneoscopy HQ in St. Louis, Missouri.

The Quality Control (QC) Specialist I i is responsible for performing quality control activities related to medical records and other quality documentation throughout the testing and manufacturing lifecycle. This role ensures accuracy, completeness, and compliance with internal procedures, regulatory requirements, and quality standards. The QC Specialist I reviews and verifies records, identifies discrepancies, and supports timely resolution to maintain data integrity and product quality. This position collaborates cross-functionally with laboratory, manufacturing, and quality teams to support efficient operations and continuous improvement within the quality management system.

RESPONSIBILITIES

• Conduct QC reviews of sample/specimen data for accuracy throughout the testing process.
• Help to provide assurance of the quality of our products by evaluating incoming materials, inspecting components and products at various stages, and evaluating the functionality of finished products using ddPCR.
• Support the laboratory and clinical operations, performing QC checks as needed on data and manual entries.
• Collaborate with laboratory personnel to update or open nonconformances for inaccurate data.
• Track and trend QC data and prepare quality presentations.
• Assist in maintaining compliance with all applicable regulations and requirements (CLIA, CAP, NYS, DOH, FDA, ISO, etc.).
• Support the Quality Management System, including but not limited to nonconformances and customer complaint processes.
• Conduct gap analyses and best practice reviews to sustain and continually improve the Quality Management System.
• Participate in internal and external audits and manufacturing inspections.
• Review incoming material release inspections.
• Navigate and execute laboratory equipment inspections.
• Review, revise, author, and implement new procedures and/or controls to achieve regulatory compliance and operational efficiency.
• Perform work under general supervision, navigating through moderately complex problems.
• Exemplify solid knowledge of the subject matter.
• Other duties as assigned.

EDUCATION REQUIREMENTS

• Bachelor's Degree within a science-related field required.
  • A degree in Biology or Chemistry is ideally preferred.

QUALIFICATIONS

• Possess 1-2 years of experience in a CLIA/CAP or QSR-regulated environment.
• Possess a minimum of 2 years of PCR testing experience.
• Demonstrate the ability to read and understand technical procedures and instructions.
• Exemplify the ability to multitask and thrive in an agile, fast-paced, deadline-driven environment while remaining flexible, proactive, resourceful, and efficient.
• Possess proficient verbal and written communication skills, while willing to share and receive information and ideas from all levels of the organization to achieve the desired results.
• Possess high ethics and conduct business in the most professional manner.
• Seek inclusiveness and collaboration but step up to responsibility, make tough decisions, and be accountable for those decisions.
• Act as a results-oriented team player with strong interpersonal and communication skills, capable of working collaboratively with colleagues.

SCHEDULE

This is a salaried position, requiring at least 40 hours per week. There may be projects that require activities beyond the standard hours.

COMPENSATION & BENEFITS

• Base salary range: annually determined based on the candidate's experience, knowledge, and abilities.
• Bonus: discretionary annual bonus based on a percentage of the employee's base salary
• Benefits: health, vision, dental, life insurance, 401k (with employer match), and paid time off.
• Company stock options

ADDITIONAL INFORMATION

Geneoscopy's Core Values

• Integrity - we do the right thing through our words, actions, and behaviors
• Courage - step up, speak up, stand out
• Agility - think and act fast, embracing change
• Passion - for our customers, our people, our work, and for excellence
• Collaboration - our differences are assets

Physical Demands

• Employees may be required to lift routine office supplies and use standard office equipment.
• Must possess the ability to sit and/or stand for long periods.
• Must possess the ability to perform repetitive motion.

Work Environment

• May have exposure to fumes and bio-hazardous material in the laboratory environment.
• May be required to handle blood-borne pathogens and general laboratory reagents.