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Qc Associate Jobs in Raleigh, NC (NOW HIRING)

Novo Nordisk

Quality Control Technician I (OPC)

Clayton, NC · On-site

$16 - $20.50/hr

Relationships Reports to Quality Control Manager. Essential Functions * Accuracy & Scientific ... Associate's Degree in a scientific field or equivalent combination of education & relevant ...

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How much do qc associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for qc associate in Raleigh, NC is $21.87, according to ZipRecruiter salary data. Most workers in this role earn between $15.91 and $26.63 per hour, depending on experience, location, and employer.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.

What are the most commonly searched types of Qc jobs in Raleigh, NC?

The most popular types of Qc jobs in Raleigh, NC are:

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For Qc Associate jobs in Raleigh, NC, the most frequently searched job titles are:

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What cities near Raleigh, NC are hiring for Qc Associate jobs?

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Qc Associate jobs near you
Infographic showing various Qc Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $45,484 per year, or $21.9 per hour.

Associate Director, QC Microbiology

KBI Biopharma, Inc.

Durham, NC • On-site

$24.75 - $32.25/hr

Full-time

Posted 9 days ago

KBI Biopharma rating

6.5

Company rating: 6.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

JOB SUMMARY
Responsible for overseeing microbiological programs and methods activities for
processes, instruments and equipment. Ensures the effective use of material,
equipment and personnel while developing products and processes at high quality
levels.
This person is responsible for the aspects of the following programs as directed by management:
  • Environmental Monitoring (Air Viable, Total Air Particulate, Surface Viable) Clean Utility Monitoring (Water Sampling, Bioburden, Conductivity, TOC, Coliform and Nitrates)
  • Compressed Gas Monitoring (Collection, Air Viable, Total Air Particulate, Dragger Tests and specific ID tests.)
  • Product Testing (Bioburden, Endotoxin, Host Purity, or Non-Host)
  • Media Release
  • Laboratory Support

It is the expectation that this position is required to be onsite full time. Additionally, this position should be in the laboratory at a minimum of 1 hour a day, 3 time per week.
JOB RESPONSIBILITIES
  • Strong understanding of monitoring programs and methods, makes detailed observations and conducts troubleshooting analysis.
  • Strong technical knowledge of programs. Makes detailed observations and carries out advanced data analysis.
  • Execute and review routine Microbial Laboratory work.
  • Utilizes technical discretion in the execution and interpretation of experiments that contribute to program goals.
  • May perform testing when required.
  • Strong documentation and technical writing skills.
  • Familiarity with current regulations and scientific literature.
  • Ensures method verifications and qualification protocols and investigations are performed appropriately. May execute testing when required.
  • Maintains current state of training prior to execution of tasks.
  • Assures proper labeling, handling, and storage of all chemical and biohazards used in the laboratory.
  • Assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures and attends all required safety and health training, including handling hazardous waste.

MINIMUM REQUIREMENTS
Bachelor of Science degree in a scientific discipline with a minimum of 13 - 15 years of technical management experience; or a Master's degree with 11 - 14 years or a Doctorate degree in Microbiology study and 9 -12 years related experience and/or equivalent training preferred. Additionally, a minimum of 5 years' managerial experience.
Also requires a demonstrated track record in the following areas:
  • Attainment of aggressive growth and profit objectives.
  • Strong orientation for Quality and Customer Service.
  • Demonstrated level of respect for individuals.
  • Demonstrated contribution to science in appropriate area.
  • High level of integrity and personal responsibility.
  • Record of Innovation.
  • Strong Collaboration and Team building skills.

Language Ability
  • Ability to read, analyze, and interpret the most complex documents and regulations.
  • Ability to respond effectively to the most sensitive inquiries or complaints.
  • Ability to write speeches and articles using original or innovative techniques or style. Ability to make effective and persuasive speeches and presentations on controversial or complex topics to senior management peer group, employee groups, and/or customers.

Reasoning Ability
  • Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems.
  • Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases.
  • Ability to deal with a variety of abstract and concrete variables.

Math Ability
  • Ability to apply advanced mathematical concepts such as exponents, logarithms, statistical analysis, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity,analysis of variance, correlation techniques, sampling theory and factor analysis.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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