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Qa Manufacturing Jobs in Raleigh, NC (NOW HIRING)

Adecco

Quality Assurance

Durham, NC

$18.50/hr

Minimum of 1 year of relevant experience in training, quality assurance, manufacturing, warehouse operations, or a related field. * Proficiency with Microsoft Excel, Word, email systems, and ...

Adecco

Quality Assurance

Durham, NC

$18.50/hr

Minimum of 1 year of relevant experience in training, quality assurance, manufacturing, warehouse operations, or a related field. * Proficiency with Microsoft Excel, Word, email systems, and ...

Adecco

Quality Assurance

Durham, NC

$18.50/hr

Minimum of 1 year of relevant experience in training, quality assurance, manufacturing, warehouse operations, or a related field. * Proficiency with Microsoft Excel, Word, email systems, and ...

Mastech Digital

Be Seen First

Quality Assurance Inspector

Clayton, NC · On-site

$20 - $25/hr

Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor ...

Belcan

Quality Assurance Inspector

Clayton, NC

$17 - $25/hr

Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor ...

Belcan

Quality Assurance Inspector

Clayton, NC

$17 - $25/hr

Quality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor ...

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 ... manufacturers, contract laboratories, and service providers. * Support regulatory (FDA, EMA) and ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Operate effectively in non-steady-state manufacturing environments, managing variability, process instability, and yield ramp challenges. Customer & Supplier Quality * Act as the primary quality ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Operate effectively in non-steady-state manufacturing environments, managing variability, process instability, and yield ramp challenges. Customer & Supplier Quality * Act as the primary quality ...

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Qa Manufacturing information

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How much do qa manufacturing jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for qa manufacturing in Raleigh, NC is $51.24, according to ZipRecruiter salary data. Most workers in this role earn between $43.70 and $57.93 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Qa Manufacturing position, and why are they important?

To thrive as a QA Manufacturing professional, you need a solid understanding of quality assurance principles, manufacturing processes, and experience with inspection techniques, usually supported by a degree or certification in a relevant technical field. Familiarity with quality management systems (like ISO 9001), statistical process control (SPC), and tools such as calipers, micrometers, and ERP software is highly advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills are crucial soft skills for this role. These attributes ensure the consistent production of high-quality products, improve process efficiency, and facilitate effective teamwork.

What is a QA Manufacturing job?

A QA Manufacturing job involves ensuring that products meet quality standards and regulatory requirements during the manufacturing process. Responsibilities typically include inspecting materials, monitoring production, conducting tests, and identifying defects or process improvements. QA professionals work closely with production teams to maintain consistency and compliance with industry standards. Their goal is to prevent defects, reduce waste, and enhance overall product quality before reaching customers.

What are some common challenges faced in a QA Manufacturing role?

Common challenges in QA Manufacturing include identifying and correcting process inconsistencies, managing strict production deadlines, and ensuring compliance with company and regulatory quality standards. You may frequently interact with cross-functional teams such as production, engineering, and supply chain to troubleshoot quality issues or implement process improvements. Staying up to date with evolving technologies and standards, as well as adapting to changing product requirements, is essential for long-term success. Overcoming these challenges not only enhances product reliability but also contributes to a more efficient and collaborative workplace.

What are popular job titles related to Qa Manufacturing jobs in Raleigh, NC? For Qa Manufacturing jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Qa Manufacturing jobs in Raleigh, NC look for? The top searched job categories for Qa Manufacturing jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Qa Manufacturing jobs? Cities near Raleigh, NC with the most Qa Manufacturing job openings:
Qa Manufacturing jobs near you
Infographic showing various Qa Manufacturing job openings in Raleigh, NC as of July 2026, with employment types broken down into 83% Full Time, 10% Part Time, 1% Temporary, 4% Contract, and 2% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $106,574 per year, or $51.2 per hour.
QA Manufacturing Specialist II

QA Manufacturing Specialist II

KBI Biopharma, Inc.

Durham, NC • On-site

Full-time

Re-posted 22 days ago

Job description

Please Note: This is a day shift opportunity that follows a 2-2-3 schedule
Job Summary
The QA Manufacturing Specialist is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems, and governmental regulations.
This position will provide a broad range of quality oversight for activities that support bulk drug substance manufacturing. This position will be responsible for on the floor review of executed records (batch record section review, solution records, equipment records, and logbooks) supporting all aspects of cGMP operations. Client and regulatory audit/inspection support is also within job scope.
Job Responsibilities
  • Perform on-the-floor compliance review on executed records including batch records, equipment preparation records, and solution record and associated forms, in-process data, and logbooks.
  • Perform activities such as manufacturing walk-throughs, facility responses, label reconciliation, etc.
  • Support Manufacturing changeover process.
  • Work directly with manufacturing, the laboratory and other departments responsible for GMP activities to resolve deviations, CAPAs, and other compliance issues in a timely manner
  • Support client audits and regulatory inspections and client batch record review process.
  • Support QA Raw Material group with release of raw materials
  • Able to react to change productively and handle other essential tasks as assigned.
  • Review document revisions (SOPs, Forms, Solution Records, etc)
  • Supports training of other Quality department staff to perform quality duties as needed.
  • Support process improvement projects to include improving the lifecycle of batch record review cycle times and batch release dates.

Minimum Requirements
  • MQA Specialist II: BS/BA in scientific field and 5 years experience or MS/MA degree and 3 years' experience in a QA GMP regulated environment within Biopharmaceuticals or equivalent is required.
  • Knowledge of US and EU cGMP guidelines/regulations is desired.
  • Experience with electronic document management systems, SAP and Microsoft Office suite are preferred.
  • Demonstrated strong interpersonal skills, ability to work in a team environment, attention to details and excellent problem resolutions skills.
  • Knowledge of biopharmaceutical manufacturing including cell culture, protein purification, and single-use platform technology is preferred.

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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