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Senior Quality Advisor Jobs in Raleigh, NC (NOW HIRING)

As a Sr. Advisor , you will be responsible for leading and executing strategic marketing projects ... Ensure brand consistency and quality: Oversee the development of marketing materials and campaigns ...

... quality standards. At Senior Owner's Advisor direction, this role will help Owner's selection of project delivery methods, plan and support market sounding and industry outreach, develop Requests for ...

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Senior Quality Advisor information

See Raleigh, NC salary details

$48.6K

$134.1K

How much do senior quality advisor jobs pay per year?

As of Sep 6, 2026, the average yearly pay for senior quality advisor in Raleigh, NC is $126,749.00, according to ZipRecruiter salary data. Most workers in this role earn between $132,700.00 and $133,200.00 per year, depending on experience, location, and employer.

What does a senior quality advisor do?

A Senior Quality Advisor is responsible for overseeing and improving quality assurance processes within an organization. They develop and implement quality management systems, conduct audits, and ensure compliance with industry standards and regulations. Additionally, they provide guidance to teams on best practices, help resolve quality issues, and drive continuous improvement initiatives. Their role is crucial in maintaining product or service excellence and supporting organizational goals.

What are the key skills and qualifications needed to thrive as a senior quality advisor?

To thrive as a Senior Quality Advisor, you need a deep understanding of quality management systems, auditing processes, and industry regulations, often supported by a degree in a relevant field and certifications like ISO 9001 Lead Auditor. Familiarity with quality management software, data analysis tools, and compliance documentation systems is typically required. Excellent communication, problem-solving, and leadership skills enable you to influence cross-functional teams and drive continuous improvements. These competencies are crucial for ensuring organizational compliance, maintaining high standards, and fostering a culture of quality.

How does a senior quality advisor typically interact with cross-functional teams to drive quality improvements?

A Senior Quality Advisor frequently collaborates with cross-functional teams, including production, engineering, and regulatory departments, to identify quality gaps and implement process improvements. They often lead meetings to review quality metrics, share findings from audits, and develop action plans with relevant stakeholders. Effective communication and consensus-building are key, as the role requires aligning team members around best practices and compliance standards. This collaborative approach not only ensures consistent product quality but also fosters a culture of continuous improvement throughout the organization.

What is the difference between Senior Quality Advisor vs Quality Specialist?

AspectSenior Quality AdvisorQuality Specialist
CredentialsTypically requires a degree in quality management, engineering, or related field; certifications like CQE or ASQ are commonSimilar credentials; often holds certifications like CQE or Six Sigma Green Belt
Work EnvironmentLeads quality initiatives, audits, and process improvements across departmentsFocuses on implementing quality procedures, inspections, and data analysis
Employer & Industry UsageUsed in manufacturing, aerospace, and industrial sectors for senior-level quality rolesCommon in manufacturing, healthcare, and service industries for quality assurance roles

The Senior Quality Advisor and Quality Specialist roles share similar credentials and work environments, but the Senior Quality Advisor typically oversees quality programs and leads strategic initiatives, while the Quality Specialist focuses on executing quality procedures and inspections. The senior role involves more leadership and decision-making responsibilities within the organization.

What job categories do people searching Senior Quality Advisor jobs in Raleigh, NC look for?

The top searched job categories for Senior Quality Advisor jobs in Raleigh, NC are:

Infographic showing various Senior Quality Advisor job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $126,749 per year, or $60.9 per hour.

Senior Specialist 2, Quality Control Instrumentation

Fujifilm

Holly Springs, NC • On-site

Full-time

Re-posted yesterday


Key responsibilities

  • Manage the qualification, routine operation, maintenance, continuous improvement, and decommissioning of QC analytical instrumentation.

  • Ensure QC equipment and instruments adhere to applicable regulatory guidelines, data integrity expectations, and site policies.

  • Partner with vendors to plan and oversee instrument maintenance activities.


Fujifilm rating

8.5

Company rating: 8.5 out of 10

Based on 70 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers


Job description

Position Overview

Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC Instrumentation, you will lead the routine operation, qualification, maintenance, continuous improvement, and decommissioning of QC analytical instrumentation with minimal supervision-while ensuring data integrity and regulatory compliance at every step.

You'll be the go-to expert for instrument performance and reliability, partnering across functions and with external vendors to solve complex problems, drive process improvements, and uphold world-class standards. This role includes periodic on-call and weekend support, as needed.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

What you'll do

  • Manage the qualification, routine operation, maintenance, continuous improvement, and decommissioning of QC analytical instrumentation.
  • Ensure QC equipment and instruments adhere to applicable regulatory guidelines, data integrity expectations, and site policies.
  • Develop, author, and review SOPs, technical reports, user requirements, functional specifications, and KNEAT protocols and reports.
  • Lead data integrity initiatives for analytical instruments, including periodic reviews to ensure ongoing compliance.
  • Recommend user roles and privileges to uphold data integrity; design instrument operating instructions and preventive maintenance plans.
  • Execute and evaluate periodic reviews of QC instruments and their control software; monitor ongoing performance and drive process improvements.
  • Partner with vendors to plan and oversee instrument maintenance activities.
  • Initiate and oversee follow-up on excursions and deviations; manage corrective and preventive actions (CAPAs) related to analytical instruments.
  • Provide guidance to stakeholders and address issues related to QC analytical instruments; manage a variety of routine tasks while balancing project priorities.
  • Collaborate with cross-functional partners-including end users, Validation, Labware Specialists, and Quality Assurance-to ensure effective, compliant instrument operations.
  • Perform other duties, as assigned.

How you'll work

  • Tackle problems of diverse scope, analyzing limited information and precedent to devise solutions and adapt approaches.
  • Apply sound evaluation, judgment, and interpretation to select the right course of action.
  • Operate independently with work reviewed at critical points.
  • Build strong relationships and networks with senior internal/external partners-often advising others on complex topics and tailoring communication to differing audiences.

Minimum education and experience requirements

  • Bachelor's in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 5+ years of experience OR
  • Master's in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 3+ years of experience OR
  • PhD in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 1+ years of experience
  • 3+ years of experience in a GMP environment
  • Prior hands-on experience with analytical instrumentation, including but not limited to UPLC/HPLC (Ultra/High-Performance Liquid Chromatography), Capillary Electrophoresis/Imaged Capillary Isoelectric Focusing (iCIEF), Gel Electrophoresis/Western Blot, Plate Readers, qPCR (Quantitative Polymerase Chain Reaction), Spectrophotometry, and Mass Spectrometry

Preferred qualifications

  • Experience qualifying analytical instruments
  • Experience with Customer Relationship Management
  • Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action [CAPA], document management system)

Why this role

  • Own a mission-critical instrument program and make measurable impact on data integrity, compliance, and QC reliability.
  • Shape best practices, steward continuous improvement, and partner across the organization and with external vendors.
  • Develop as a trusted advisor who solves complex challenges and advances operational excellence.

Work schedule

  • Includes periodic on-call and weekend support, as needed.

Ready to lead the instruments that power high-quality science? Apply now.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

Employment Type: OTHER

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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