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Manufacturing Quality Manager Jobs in Raleigh, NC

Symbiotic Services

Quality Tecnician

Raleigh, NC · On-site

$17.50 - $23.50/hr

... to support manufacturing quality systems, inspection processes, and continuous improvement ... Manage nonconforming materials and MRB processes Assist with root cause analysis and corrective ...

Eaton

Senior Quality Engineer

Youngsville, NC · On-site

$86K - $126K/yr

Work with Manufacturing Quality, Receiving, Purchasing, and Engineering to manage and control incoming material and assist with supplier NCM inventory disposition. Resolve component issues with ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Ensure adherence to regulatory and safety requirements specific to Li-ion battery manufacturing. Quality Management Systems (QMS) * Oversee document control, change management, and internal audit ...

DivIHN Integration Inc

Quality Engineer I

Durham, NC · On-site

$69K - $89K/yr

This position works closely with other functions within the organization (Manufacturing, R&D, ... Ability to work independently with strong time management and prioritization skills to handle ...

Forge Nano

Director of Quality Assurance

Raleigh, NC · On-site

Ensure adherence to regulatory and safety requirements specific to Li-ion battery manufacturing. Quality Management Systems (QMS) * Oversee document control, change management, and internal audit ...

MSD

Director, External Quality - Remote

Durham, NC · Hybrid

In this role you will be subject matter expert in EQA and manufacturing quality systems, technology platforms, regulatory expectations, and external manufacturing management, with the opportunity to ...

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Manufacturing Quality Manager information

See Raleigh, NC salary details

$63.2K

$97.9K

$124.9K

How much do manufacturing quality manager jobs pay per year?

As of Jun 17, 2026, the average yearly pay for manufacturing quality manager in Raleigh, NC is $97,895.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,100.00 and $111,800.00 per year, depending on experience, location, and employer.

What are the most common challenges a Manufacturing Quality Manager faces in a typical day?

Manufacturing Quality Managers often navigate challenges such as maintaining consistent product quality during high-volume production, investigating and resolving quality issues quickly, and ensuring compliance with changing industry standards. They regularly collaborate with production, engineering, and supply chain teams to implement process improvements and corrective actions. Balancing quality expectations with tight deadlines and cost pressures can be demanding, but effective managers use data-driven strategies and strong teamwork to achieve results. This role is dynamic and requires adaptability, attention to detail, and a commitment to ongoing process optimization.

What does a Manufacturing Quality Manager do?

A Manufacturing Quality Manager ensures that products meet quality standards and regulatory requirements in a production environment. They develop and implement quality control processes, conduct audits, and analyze data to identify areas for improvement. They also collaborate with teams to resolve production issues and enhance efficiency while maintaining compliance. Their role is crucial in minimizing defects, improving customer satisfaction, and ensuring operational excellence.

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

To thrive as a Manufacturing Quality Manager, you need strong knowledge of quality assurance processes, regulatory compliance, and manufacturing operations, usually supported by a bachelor's degree in engineering or a related field. Familiarity with quality management systems (like ISO 9001), statistical process control, Six Sigma methodologies, and relevant certifications such as CQE or Lean are commonly required. Strong leadership, problem-solving skills, and effective communication help you excel in team settings and drive continuous improvement initiatives. These competencies ensure consistent product quality, support regulatory requirements, and foster a culture of excellence on the manufacturing floor.

What are popular job titles related to Manufacturing Quality Manager jobs in Raleigh, NC? For Manufacturing Quality Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Manufacturing Quality Manager jobs in Raleigh, NC look for? The top searched job categories for Manufacturing Quality Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Manufacturing Quality Manager jobs? Cities near Raleigh, NC with the most Manufacturing Quality Manager job openings:
Manufacturing Quality Manager jobs near you

QA Specialist

PharmEng Technology Americas

Holly Springs, NC • On-site

Contractor

Posted 15 days ago

Job description

QA Specialist

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products.

At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals.

Responsibilities

  • Function as primary FLQA and Quality Management System (QMS) subject matter expert to assigned area(s) of responsibility within Bulk Manufacturing, QC laboratories, Fill Finish Manufacturing, Facilities, and Warehouse operations.
  • Perform quality oversight and approval of Deviations, CAPAs, and Change Controls in collaboration with Record Owners. Ensure investigations, cause identification, CAPA development, and accurate change controls within Bulk, QC, Fill Finish, FacOps, and Warehouse departments.
  • Track closure of assigned QMS records.
  • Participate in suite team meetings, provide FLQA support for projects and initiatives.
  • Conduct on-the-floor walkthroughs and coaching to instill a quality mindset, compliance knowledge, and a strong quality culture among manufacturing staff.
  • Bring adherence to and continuous improvement of quality systems within Bulk, QC, Fill Finish, FacOps, and Warehouse departments.
  • Support development, revision, and implementation of SOPs, protocols, and other GMP documents.
  • Help deliver Deviation, CAPA, and Change Control Annual Product Quality Review (APQR) sub-reports.
  • Lead continuous improvement projects, offer quality support to site capital projects and global quality system improvements.
  • Ensure inspection readiness through routine quality walkthroughs, monitoring adherence, and direct involvement in Site Self Inspections.
  • Be a QA SME for internal and external audits.
  • Proficiently use computerized systems including TrackWise, Veeva QMS and QDocs, GLIMS, SAP, CMMS.
  • Provide support to greater FLQA organization, including quality oversight of Bulk Manufacturing/QC Laboratories and QA reviews of batch records and GMP records at the site.
  • Acquire and maintain knowledge of current local and international regulatory requirements/trends, ensuring advice and technical support on quality/compliance matters are provided to the site.

Requirements

  • Bachelor's degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry) preferred or equivalent experience in biotech or pharmaceutical industry
  • 3+ years' GMP experience in the pharmaceutical/biotech industry
  • Previous experience directly working in the industry or having direct responsibilities approving GMP deviations, CAPAs, and change controls.
  • Previous experience in root cause analysis and risk management, including working experience of root cause analysis tools such as Fishbone/5Why
  • Previous experience in quality role in an FDA regulated manufacturing or laboratory setting or an understanding of the quality requirements for the pharmaceutical industry.
  • Experience with the production processes used in pharmaceutical parenteral drug product manufacturing.