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Associate Quality Control Analyst Jobs in Raleigh, NC

QC Microbiology Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Durham NC USA 27712 Description of Responsibilities Position Summary The QC Microbiology Analyst 1 ... Associate's Degree 0 Bachelor's Degree 0 Master's Degree 0 Doctorate 0 Post Doctorate 0 ...

Applied Research Associates (ARA), Inc. is seeking a qualified Program Control Analyst to join the project management team at ARA's Software Enterprise Division (SED) Raleigh, NC location. This is a ...

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Associate Quality Control Analyst information

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How much do associate quality control analyst jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for associate quality control analyst in Raleigh, NC is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $22.45 and $30.14 per hour, depending on experience, location, and employer.

Is QC a high paying job?

The salary for an Associate Quality Control Analyst varies by industry, location, and experience, but it is generally considered an entry- to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or managerial responsibilities within quality control roles.

What is the role of associate quality analyst?

An associate quality control analyst is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to improve processes, often using tools like laboratory equipment or quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are some common challenges faced by Associate Quality Control Analysts during routine testing, and how can they be addressed?

Associate Quality Control Analysts often encounter challenges such as tight deadlines, managing multiple sample types, and handling complex analytical instruments. Staying organized and maintaining clear documentation helps manage workflow efficiently. Regular calibration and maintenance of laboratory equipment, along with ongoing training, are essential to minimize errors and ensure accurate results. Collaborating closely with senior analysts and cross-functional teams can also help troubleshoot unexpected issues and streamline processes.

How much is the salary of a QA analyst?

The salary of an Associate Quality Control Analyst typically ranges from $50,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of quality standards and testing tools.

What is the difference between Associate Quality Control Analyst vs Quality Control Technician?

AspectAssociate Quality Control AnalystQuality Control Technician
CredentialsBachelor's degree in life sciences or related field; certifications like CQE are commonHigh school diploma or associate degree; technical certifications may be preferred
Work EnvironmentLaboratories, manufacturing facilities, quality assurance departmentsManufacturing sites, laboratories, production lines
Job ResponsibilitiesData analysis, documentation, reviewing quality processes, supporting auditsPerforming tests, inspecting products, recording test results

While both roles support quality assurance, the Associate Quality Control Analyst typically focuses on data analysis and documentation, whereas the Quality Control Technician primarily conducts tests and inspections. The analyst role often requires a higher level of education and analytical skills, making it suitable for those interested in quality systems and compliance.

What does an Associate Quality Control Analyst do?

An Associate Quality Control Analyst is responsible for testing and inspecting products, materials, or processes to ensure they meet established quality standards. They perform routine laboratory tests, document results, and identify any deviations from specifications. These analysts often work in industries like pharmaceuticals, manufacturing, or food production, supporting senior analysts and quality managers. Their role is crucial in maintaining product safety, consistency, and regulatory compliance.

What is a QC analyst salary?

A Quality Control (QC) analyst salary varies depending on experience, location, and industry, but typically ranges from $50,000 to $70,000 annually in many regions. Entry-level positions may start lower, while experienced analysts with certifications can earn higher wages, often supplemented by benefits and overtime opportunities.

What are the key skills and qualifications needed to thrive as an Associate Quality Control Analyst, and why are they important?

To thrive as an Associate Quality Control Analyst, you need a solid background in biology, chemistry, or a related scientific field, often with a relevant bachelor's degree. Familiarity with laboratory equipment, quality management systems (such as LIMS), and regulatory guidelines like GMP is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying and resolving quality issues. These skills and qualifications ensure accuracy, compliance, and consistent product quality in laboratory and manufacturing environments.
What are the most commonly searched types of Quality Control Analyst jobs in Raleigh, NC? The most popular types of Quality Control Analyst jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Associate Quality Control Analyst jobs? Cities near Raleigh, NC with the most Associate Quality Control Analyst job openings:
Senior Quality Control Analyst I, Analytical Methods

Senior Quality Control Analyst I, Analytical Methods

Beam Therapeutics

Durham, NC

Other

Posted 8 days ago


Job description

Position Overview:

Beam is seeking a highly motivated and energetic Senior Analyst to join the QC analytical team.  The Senior Quality Control Analyst, Analytical Methods will primarily support critical analytical method implementation workstreams including method qualification, validation, and transfers to enable start-up and scale-up of cGMP manufacturing operations across multiple site programs. The Senior Analyst will work collaboratively with cross-functional teams to plan and execute method qualification and validation activities to drive program advancement and support critical company milestones.

In addition to method lifecycle-focused work, this role will contribute to routine GMP testing ensuring continuity of QC support for both in-process, release and stability testing. This role will also support routine laboratory operations including reagent receipt, inventory management and equipment maintenance. This position will support change controls, deviations, investigations as well as implementation of continuous improvements.

The Senior Analyst will work closely with team members in Quality Assurance, Manufacturing, MS&T and Analytical Development.  The Senior Analyst is expected to be an on-site resource at Beam's manufacturing facility in RTP, North Carolina.

Responsibilities:

  • Collaborate with cross-functional partners (Quality Assurance, Manufacturing, MS&T and Analytical Development) to support and execute strategy for analytical method lifecycle activities, ensuring alignment with program milestones and timelines.
  • Lead and perform analytical method qualifications, validations, and transfers to support program startup, scale-up, and lifecycle management across multiple programs.
  • Author and review validation protocols, reports, and supporting GMP documentation, ensuring accuracy, completeness, and compliance with internal procedures and regulatory expectations.
  • Execute routine GMP testing to support in-process, release, and stability in accordance with approved methods, specifications, and SOPs.
  • Perform a range of bioanalytical methods including flow cytometry, cell count, HPLC, plate-based ELISAs, etc.
  • Document all testing activities accurately and contemporaneously in laboratory systems (e.g., LIMS, LES) and assay data sheets, ensuring adherence to ALCOA+ principles.
  • Analyze and interpret data within given parameters; escalate unexpected results to area manager and provide support for deviation initiation, investigations, root cause analysis and CAPA implementation.
  • Initiate and drive change control activities related to analytical methods, procedures, equipment, and systems as required.
  • Maintain routine laboratory operations, including reagent receipt, inventory management, and general lab upkeep in a GMP environment.
  • Perform and support QC laboratory instrument maintenance including cleaning, calibration preventative maintenance according to pre-established maintenance schedules.
  • Identify and support implementation of continuous improvement opportunities to enhance analytical methods, laboratory processes, and operational efficiency.
  • Communicate technical information and issues clearly to peers, supervisors, and cross-functional stakeholders to support timely decision-making.

Qualifications:

  • Bachelor's degree required, preferably in biology, chemistry, life science, or related discipline.
  • 6+ years relevant bioanalytical assay experience in methods such as flow cytometry, HPLC, ELISAs, etc.
  • Prior GMP experience is preferred.
  • Advanced technical writing skills and problem-solving ability.
  • Ability to work independently in a high-paced team environment, meet deadlines, and prioritize tasks across multiple projects.
  • Advanced ability to communicate effectively with peers and demonstrate collaboration across multiple cross-functional groups.