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Qc Quality Control Jobs in Raleigh, NC (NOW HIRING)

QC Lead Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Description QC Lead Analyst Position Summary The Quality Control (QC) Biochemistry Lead Analyst provides front-line leadership for the QC Biochemistry team performing routine testing of raw materials ...

QC Lead Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Description QC Lead Analyst Position Summary The Quality Control (QC) Biochemistry Lead Analyst provides front-line leadership for the QC Biochemistry team performing routine testing of raw materials ...

QC Tech IV

Raleigh, NC · On-site

$18.25 - $23.25/hr

Assists with QC Lab Hazardous Waste program. * Stocks laboratory chemicals and helps with checking inventory levels for ordering needs. * Assists QA as needed. * Performs specified analysis on all ...

We are seeking a Quality Control Managerfor our facility in Apex, NCthat will provide Quality Management (QM) related services. In this role, you will be involved in daily operations to plan and ...

QC Lead Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Description QC Lead AnalystPosition Summary The Quality Control (QC) Biochemistry Lead Analyst provides front-line leadership for the QC Biochemistry team performing routine testing of raw materials ...

We are seeking a Quality Control Managerfor our facility in Apex, NCthat will provide Quality Management (QM) related services. In this role, you will be involved in daily operations to plan and ...

We are seeking a Quality Control Manager for our facility in Apex, NC that will provide Quality Management (QM) related services. In this role, you will be involved in daily operations to plan and ...

We are seeking a Quality Control Manager for our facility in Apex, NC that will provide Quality Management (QM) related services. In this role, you will be involved in daily operations to plan and ...

QA/QC for Construction

Chapel Hill, NC · On-site

$71K - $94K/yr

QA/QC for Construction Benefits: Medical, Dental, PTO, 401K, Sick Time Quality Assurance (QA): Willing to travel to jobsites. Review and fully understand job specifications, submittals, and drawings ...

Overview / Responsibilities Wood Programs, Inc. (WPI) is seeking a Quality Control Manager to join our team in Durham, NC. Key Responsibilities: * Coordinate with Quality Inspector for progress of on ...

Responsibilities include daily quality control reporting, subcontractor management, submittal management, conducting quality phase meetings and frequent field quality control inspections aimed at ...

Showing results 41-60

Qc Quality Control information

See Raleigh, NC salary details

$29.6K

$79.1K

$125.9K

How much do qc quality control jobs pay per year?

As of Aug 12, 2026, the average yearly pay for qc quality control in Raleigh, NC is $79,053.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,800.00 and $97,200.00 per year, depending on experience, location, and employer.

Is quality control a high paying job?

Quality control jobs, including roles like QC inspector or technician, typically offer average to above-average wages depending on industry, experience, and location. Advanced certifications and specialized skills can lead to higher salaries in this field.

Do you need a degree for Qc Quality Control?

A degree is not always required for a Quality Control (QC) position, but many employers prefer candidates with a high school diploma or equivalent, along with relevant technical training or certifications. Skills in inspection, attention to detail, and knowledge of industry standards are often more important than formal education for QC roles.

What is the difference between Qc Quality Control vs Quality Assurance?

AspectQc Quality ControlQuality Assurance
Primary FocusInspecting products and identifying defectsPreventing defects through process improvements
CertificationsOften requires certifications like ASQ CQE or CQASimilar certifications, emphasizing process management
Work EnvironmentManufacturing, production lines, labsQuality management systems, audits, process reviews
Industry UsageManufacturing, construction, pharmaceuticalsManufacturing, software, service industries

While both roles aim to ensure product quality, Qc Quality Control focuses on inspecting and testing products for defects, whereas Quality Assurance emphasizes establishing processes to prevent defects from occurring. Both roles often require similar certifications and are integral to quality management in various industries.

Is QA QC a good career?

Quality Control (QC) and Quality Assurance (QA) roles are essential in manufacturing, construction, and software industries, focusing on maintaining product standards and compliance. These careers often require attention to detail, technical skills, and certifications such as ISO or Six Sigma, and can offer stable employment with opportunities for advancement. Overall, QA/QC can be a good career choice for individuals interested in ensuring quality and safety in various industries.

What is the job of quality control (QC)?

A quality control (QC) professional is responsible for inspecting and testing products or materials to ensure they meet specified standards and quality requirements. They identify defects, document issues, and work with production teams to improve processes, often using tools like measurement instruments and quality management systems. QC roles typically require attention to detail and knowledge of industry standards and certifications.
What are popular job titles related to Qc Quality Control jobs in Raleigh, NC? For Qc Quality Control jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Qc Quality Control jobs? Cities near Raleigh, NC with the most Qc Quality Control job openings:
Infographic showing various Qc Quality Control job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $79,053 per year, or $38 per hour.

QC Lead Analyst

bioMérieux

Durham, NC • On-site

$23.25 - $31.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


bioMérieux rating

8.1

Company rating: 8.1 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

117th of 538 rated manufacturers


Job description

Description
QC Lead Analyst
Position Summary
The Quality Control (QC) Biochemistry Lead Analyst provides front-line leadership for the QC Biochemistry team performing routine testing of raw materials, intermediates, finished goods, and stability samples. The role oversees and may execute testing while ensuring regulatory compliance, accurate documentation, and proper use of validated and calibrated instrumentation. The Lead Analyst applies advanced analytical and regulatory expertise to optimize methods and lead high-complexity OOS, NCMR, CI, and CAPA investigations. They are responsible for developing employees, managing projects, maintaining laboratory operations, driving accountability for team performance, and leading quality initiatives that improve testing processes. This position enhances departmental productivity, efficiency, testing quality, and culture by identifying inefficiencies, adapting workflows, and collaborating across the organization to drive productivity and continuous improvement.
Primary Duties
  • Provides front-line leadership for the QC Biochemistry team, serving as backup to the QC Manager and overseeing daily scheduling, shift meetings, accountability for team performance, and Quality decisions.
  • Develops, mentors and trains, and motivates employees to achieve high performance, foster internal growth, and maintain alignment with current QC processes and procedures.
  • Oversees and may execute routine Biochemistry testing of raw materials, intermediates, finished goods, and stability samples while ensuring regulatory compliance and accurate documentation from the QC Biochemistry team.
  • Manages laboratory operations, including scheduling special testing requests, inventory maintenance, and ensuring proper use, maintenance, and troubleshooting of validated and calibrated instrumentation.
  • Ensures all testing documentation is thorough, timely, and GDP-compliant, and maintains high standards of data integrity across all QC activities.
  • Leads or oversees high-complexity investigations, including OOS, NCMR, CI, and CAPA, and supports audits as a subject matter expert using advanced analytical and regulatory knowledge.
  • Recommends and authors SOP revisions and process improvements, supports LIMS data entry, maintenance, and review, and ensures team training remains current and compliant with departmental requirements.
  • Enforces safety policies, ensures proper PPE use, and maintains a clean, organized, and cGLP-compliant audit-ready laboratory environment.
  • Drives continuous improvement by identifying inefficiencies, adapting workflows, and participating in cross-functional initiatives to enhance productivity, efficiency, testing quality, and departmental culture.
  • Supports departmental goal setting, validation activities, and other duties assigned by management to maintain operational readiness and quality standards.
  • Perform all work in compliance with company quality procedures and standards.
  • Perform other duties as assigned.
Qualifications
Required Education, Training and Experience
  • Bachelor's degree and no previous experience required. Bachelor's degree highly preferred in Chemistry, Biochemistry, or Biomedical.
  • Education Substitution: In lieu of a Bachelor's degree, 4+ years of additional relevant experience, defined below, will be accepted.
  • Experience working in a regulated Biochemistry or Chemistry laboratory (FDA, ISO, USDA, etc.) with GxP testing.
Preferred Education, Training and Experience
  • Proven technical and scientific knowledge working with relevant Chemistry and/or Biochemistry laboratory techniques and quality principles (GMP/GLP) preferred.
  • Demonstrates strong knowledge of domestic and international regulations and industry standards (ISO, QSR, UL, CSA, VDE) and has experience supporting regulatory audits such as FDA, MDSAP, ISO, OSHA, and EPA.
  • Extensive experience in the use of software tools for data entry and analysis (LIMS); advanced technical writing skills.
  • Shows strong organizational, leadership, and interpersonal abilities - training and developing staff, prioritizing multiple tasks, planning testing schedules, collaborating across levels, and authoring/redlining SOPs.
  • Exhibits advanced analytical, problem-solving, documentation, and investigation skills, including data trending, report preparation, GDP compliance, and effective verbal and written communication.
  • Strong organizational, communication, and leadership skills with the ability to prioritize work, manage multiple tasks independently, and effectively collaborate in team-oriented environments.
  • Proven ability to interpret, execute, and update SOPs, lead improvement initiatives, assess safety and environmental risks, and independently problem-solve and provide solutions with minimal supervision.
Key Skills (Knowledge, Skills & Abilities)
  • Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes.
  • Written Communications - including the ability to communicate technical data in written form.
  • Effective Presentation Skills - including the ability to present technical data.
  • Leading without authority through influence and guidance of others towards a common goal by using expertise, persuasion, and personal qualities to inspire action.
  • Managing and measuring work by tracking progress, performance, and goal achievement using metrics and KPIs.
  • Inspire and energize individuals to achieve their best performance.
  • Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel.
    • Expert: leads in applying technology; innovates, optimizes processes, and trains others.
Working Conditions & Physical Requirements
Physical Requirements
  • Ability to remain in stationary position, either sitting or standing, for prolonged periods.
  • Ability to ascend/descend stairs, ladders, ramps, and the like.
  • Ability to wear PPE correctly most of the day.
  • Ability to operate heavy machinery. No
  • Ability to adjust or move objects up to 50 pounds in all directions.
Travel Requirements
  • Domestic travel required: 0%
  • International travel required: 0%
  • Total travel: 0%
Additional Position Information
  • This position is in a fast-paced, FDA regulated environment in the Medical Devices/Diagnostics Industry.
  • The QC Biochemistry Lead Analyst is a key position in the Biochemistry laboratory performing testing of Description, pH, FTIR, Osmolality, Moisture Analysis, Solubility, Loss on Drying, Resin Ratio, Reflectance, and pO2 Headspace Analysis, HPLC.
Reports To
QC Manager, Biochemistry/BCID
Supervisory Responsibilities
  • Direct supervision: 0 (Not applicable)
  • Indirect supervision: 0 (Not applicable)

The salary range for this role in the state of North Carolina is $58,700 to $88,000 annually. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMérieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer.
In addition, bioMérieux offers a competitive Total Rewards package that may include:
• A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options
• Company-Provided Life and Accidental Death Insurance
• Short and Long-Term Disability Insurance
• Retirement Plan including a generous non-discretionary employer contribution and employer match.
• Adoption Assistance
• Wellness Programs
• Employee Assistance Program
• Commuter Benefits
• Various voluntary benefit offerings
• Discount programs
• Parental leaves
#biojobs
Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at [email protected].
BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

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