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Qa Manufacturing Jobs in Raleigh, NC (NOW HIRING)

QA Operations Sr. Manager

Raleigh, NC · On-site

$90 - $120/hr

Ensure QA presence in operations through Manufacturing QA and other QA Operations teams. * Translate regulatory expectations into practical, meaningful practices. * Promote proactive identification ...

The QA Specialist, Drug Product (DP) helps drive the Quality oversight for the direction of all DP Manufacturing processes through to operational readiness during project phase. This role oversees QA ...

Position Overview The QA Operations Specialist is responsible for providing quality oversight of ... Whether your expertise lies in research, manufacturing, or production, you'll find a home here ...

QA Training Specialist

Morrisville, NC · On-site

$18.50 - $19.88/hr

High School Diploma or GED (required) * 2-4 years of experience in quality assurance, training, manufacturing, or a related environment * Strong communication, coaching, and organizational skills

New

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Qa Manufacturing information

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$78

How much do qa manufacturing jobs pay per hour?

As of Sep 7, 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 is a QA manufacturing?

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 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.

Is QA manufacturing a stressful job?

QA manufacturing can be stressful due to the responsibility of ensuring product quality and compliance with standards, often involving strict deadlines and attention to detail. The role requires focus, problem-solving skills, and sometimes working in fast-paced environments, but stress levels vary depending on the company and workload.

What is the role of QA in manufacturing?

The QA (Quality Assurance) role in manufacturing involves monitoring and inspecting products and processes to ensure they meet quality standards and specifications. QA professionals develop testing procedures, perform audits, and document findings to prevent defects and improve product reliability. They often use tools like inspection equipment and quality management systems to maintain consistent product quality.

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 cities near Raleigh, NC are hiring for Qa Manufacturing jobs?

Cities near Raleigh, NC with the most Qa Manufacturing job openings:

Infographic showing various Qa Manufacturing job openings in Raleigh, NC as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $106,574 per year, or $51.2 per hour.

Quality Engineer II-III, Quality Assurance

MedPharm

Durham, NC • On-site

Full-time

Posted 14 days ago


Job description

Position Summary
Quality Engineer II-III, Quality Assurance is responsible for designing, implementing, and maintaining the Quality Management System across the manufacturing lifecycle. This role supports process validation; root-cause investigations for deviations; oversees Corrective and Preventive Actions; and ensures compliance with current Good Manufacturing Practices. This position is responsible for monitoring and control the quality processes supporting incoming, in-process and final disposition including batch record review and release for GMP, clinical, and commercial programs through broad knowledge of GLP/GMP manufacturing theories and principles. This position works closely with other functional areas of the Company to release raw materials, per agreed upon timelines. Additional areas of responsibility include QA oversight of operational metrics and supporting client and internal auditing activities. The Quality Engineer II-III, Quality Assurance shall adhere to the Company's quality system including but not limited to the applicable standards, policies and procedures in the areas of responsibility defined in this job description.
Essential Functions
  • Regulatory Compliance: Ensure all production practices strictly align with FDA 21 CFR Parts 210/211, ICH Q10, and global cGMP standards.
  • Validation & Qualification: Quality Assurance review and approval of validation protocols (IQ/OQ/PQ) for manufacturing equipment, facilities, utilities, and analytical laboratory software.
  • Deviation & CAPA Management: Support investigation of manufacturing deviations and out-of-specification (OOS) results using root-cause analysis tools like 5 Whys and Fishbone diagrams.
  • Documentation: Quality Assurance review and approval of manufacturing documentation, including specifications, batch records, and batch release.
  • Risk Assessment: Support Quality Risk Management (QRM) initiatives utilizing Failure Mode and Effects Analysis (FMEA) to minimize patient and product risk.
  • Change Control Oversight: Evaluate and approve change controls for processes, materials, or equipment to ensure they do not negatively impact product quality.
  • Audit Support: Conduct routine internal audits and manage readiness documentation for external regulatory agency inspections.
  • Supplier Quality: Partner with procurement to audit third-party raw material suppliers and manage external quality issues.
  • Oversee the quality management processes ensuring that client requirements, specifications, and regulatory requirements are met by the Operations Unit.
  • Collaborate with cross-functional teams, including production, engineering, supply chain, and customer service, to address quality issues and drive continuous improvement initiatives.
  • Analyze quality data and performance metrics to identify trends, root causes of defects, and opportunities for process optimization.
  • Partner with Operations supporting closure of Quality Events and quality improvement plans when needed.
  • Conduct regular audits to monitor compliance with quality standards and identify areas for improvement.
  • Routinely draft and revise standard operating procedures and QA review of master batch records.
  • Leads internal and supports external audits in accordance with Company procedures and schedules. Develop reports of audit findings and communicate these to the relevant project team and to Company management

Direct Reports: No
Indirect Reports: No
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
  • Manufacturing Operations
  • Warehouse
  • Quality Control

Travel requirements
  • N/A

Education and Experience
  • B.A. / B.S. in a Engineering discipline, or equivalent experience preferred
  • Quality Assurance experience in the pharmaceutical industry for 5 +years

Knowledge, Skills, and Abilities
  • Knowledge of Pharmaceutical Quality Management Systems requirements and execution
  • Demonstrated proficiency in written, verbal and face-to-face communication to effectively present information to internal and external customers
  • Ability to successfully manage multiple tasks and multifunctional resources concurrently while maintaining high attention to detail while responding to rapidly changing priorities and aggressive deadlines
  • Technically capable of identifying root cause of a problem, offering potential solutions, and engaging with others to resolve the problem
  • Produces consistent, high quality and quantity of outputs and meaningful results that contribute to the agency mission and strategic goal. Is efficient in producing results that are delivered on time or before.
  • Ability to work independently and as part of a team
  • Expertise in MS Office (Excel, Word, Outlook, Project) and Adobe Pro

Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
  • Requires frequent standing
  • Requires constant walking
  • Requires occasional sitting
  • Requires frequent carrying, bending, twisting, reaching, & gripping
  • Requires frequent lifting, pushing, & pulling 20-60 LBS

Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.
Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.