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Qc Associate Jobs in Raleigh, NC (NOW HIRING)

Director, Site Quality - Raleigh

Raleigh, NC ยท On-site

$120 - $150/hr

... site associates.* Establishes and measuring/ reporting on the effectiveness of the QMS.* Independently and objectively reports on product quality and compliance state-of-control of the site.

... associates. * Establishes and measuring/ reporting on the effectiveness of the QMS. * Independently and objectively reports on product quality and compliance state-of-control of the site.

... associates. * Establishes and measuring/ reporting on the effectiveness of the QMS. * Independently and objectively reports on product quality and compliance state-of-control of the site.

... Control Lead Tasks: Under general supervision, resolves most problems but refers more complex issues to higher levels Process documents through Electronic Document Management Systems (EDMS) Quality ...

Traffic Control Engineer

Raleigh, NC ยท On-site

$15 - $20.25/hr

... quality control process. Minimum Qualifications: * Bachelor's or Master's degree in Civil ... Past experience managing and training younger staff/associates. Preferred Qualifications: * North ...

Traffic Control Engineer

Raleigh, NC ยท On-site

$15 - $20.25/hr

... quality control process. Minimum Qualifications: * Bachelor's or Master's degree in Civil ... Past experience managing and training younger staff/associates. Preferred Qualifications: * North ...

Traffic Control Engineer

Raleigh, NC ยท On-site

$15 - $20.25/hr

... quality control process. Minimum Qualifications: * Bachelor's or Master's degree in Civil ... Past experience managing and training younger staff/associates. Preferred Qualifications: * North ...

Showing results 41-60

Qc Associate information

See Raleigh, NC salary details

$9

$21

$32

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:

What are popular job titles related to Qc Associate jobs in Raleigh, NC?

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

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

Cities near Raleigh, NC with the most Qc Associate job openings:

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.

Senior QC Analyst (2nd Shift) - In-Process

NCBiotech

Durham, NC โ€ข On-site

$85 - $110/hr

Other

Posted 2 days ago

New


Job description

This role contains the following responsibilities covering 2nd shift hours (2:00 pm through 10:30 pm), Monday through Friday:

The Senior QC Analyst (2nd Shift) will be trained to execute analytical test methods and their corresponding analytical techniques. The core function is composed of completing QC testing for in-process, characterization, release, or stability samples. Additionally, when need arises, Senior QC Analyst will assist with troubleshooting and support In-process Support Associates with STAT samples during 2nd shift.

Responsibilities include:
  • In-process, characterization, stability, and/or release testing as assigned. Capabilities include (but not limited to) HPLC, ELISA, qPCR, SoloVPE, other spectrophotometric techniques, capillary electrophoretic techniques, and compendial testing per USP with near-zero error and minimal guidance or direction
  • Execution of method transfer, method qualification, and/or method validation testing performed under protocol
  • Solution preparation
  • Organizes and processes samples according to GxP standards
  • Independent analysis and collation of data to draw conclusions
  • Enter data into control charts and LIMS, if applicable
  • Supports lab investigation and deviation reports
  • Supports implementation of Corrective and Preventive Actions
  • Revises SOPs and technical documents
  • Supports team to troubleshoot testing or project challenges with comfort in presenting and communicating data
  • Tracks department metrics upon request; actively engages in improvement of department metrics
  • Partakes in continuous improvement projects or leading simple improvement projects
  • Ensures state of safety and regulatory audit readiness at all times
  • Maintains work to current Good Manufacturing Practices (cGMP)
  • Ensures Trainer qualification status to expand team matrix
  • Laboratory support โ€“ ensures areas are neat, clean, organized, and equipment is functioning
  • Participates in data review activities
  • Duties may include support in STAT testing coordination
  • It is the expectation that this position is required to be onsite full time with a minimum of 75% of time in the laboratory/facility
Minimum Requirements:

Relevant degree and 4-8 yearsโ€™ biopharmaceutical industry experience, preferably in protein analytics

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

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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