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Analytical Quality Assurance Jobs (NOW HIRING)

Artius Solutions

Analytical QA Supervisor

Fall River, MA · On-site

$78K - $99K/wk

Analytical QA Supervisor Location: Fall River, MA Experience Required: 5 - 15 Years Job Type: Full-time | On-site Shift: General (8:30 AM - 5:00 PM; flexibility required as per business needs ...

Cipla

Analytical QA Associate I

Fall River, MA · On-site

$66K - $86K/yr

The Analytical Quality Assurance (AQA) associate I position is an team contributor role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla ...

MetroPlusHealth

Quality Assurance Analyst

Manhattan, NY · On-site

$85K - $95K/yr

This Quality Assurance Analyst will be responsible for reviewing the Claims Processing Systems for ... Excellent analytical ability. * Excellent interpersonal, customer service and time management ...

MetroPlusHealth

Quality Assurance Analyst

Manhattan, NY · Remote

$85K - $95K/yr

This Quality Assurance Analyst will be responsible for reviewing the Claims Processing Systems for ... Excellent analytical ability. * Excellent interpersonal, customer service and time management ...

True Helix

Quality Assurance Analyst

Delmont, PA

My Account Job Openings >> Quality Assurance Analyst Quality Assurance Analyst Summary Title ... Strong analytical and problem-solving skills * Excellent verbal and written communication skills

Litehouse

Manager, Quality Assurance

Danville, VA · On-site

$99K - $149K/yr

Ensure Every Bite Counts as Quality Assurance Manager at Litehouse. Location: Danville, VA ... Analyze quality performance using statistical process control and other tools * Respond to customer ...

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Analytical Quality Assurance information

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How much do analytical quality assurance jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for analytical quality assurance in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is the difference between Analytical Quality Assurance vs Quality Control Analyst?

AspectAnalytical Quality AssuranceQuality Control Analyst
Primary FocusEnsuring processes meet quality standards and complianceTesting and inspecting products for defects
ResponsibilitiesDeveloping protocols, audits, process improvementsSampling, testing, and reporting product quality
Work EnvironmentLaboratories, manufacturing facilities, regulatory settingsLaboratories, production lines, quality labs
CertificationsGMP, GLP, ISO standards often requiredGMP, GLP, ISO certifications common

Analytical Quality Assurance focuses on maintaining and improving quality processes, while Quality Control Analysts primarily perform product testing. Both roles require similar certifications and work environments, but their core functions differ: one ensures process compliance, the other verifies product quality.

What are top 3 skills for a QA analyst?

A QA analyst should have strong attention to detail, excellent analytical and problem-solving skills, and proficiency in testing tools and methodologies. Good communication skills are also essential for documenting issues and collaborating with development teams. Familiarity with scripting or automation tools can enhance testing efficiency.

Is QC a high paying job?

Quality Control (QC) roles in industries like manufacturing and pharmaceuticals can offer competitive salaries, especially with experience and certifications. However, pay levels vary based on location, industry, and level of responsibility, and QC positions are generally considered mid-range in terms of compensation compared to other technical roles.

What is the QA analyst salary?

The average salary for a QA analyst typically ranges from $50,000 to $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications and skills in testing tools can earn higher salaries.

How does an Analytical Quality Assurance professional typically collaborate with laboratory and production teams to ensure product quality?

Analytical Quality Assurance professionals work closely with laboratory analysts and production staff to ensure that all processes meet regulatory and company quality standards. This collaboration often involves reviewing testing protocols, auditing lab practices, providing feedback on analytical results, and addressing deviations or non-conformances. By maintaining open communication and coordinating on investigations or process improvements, AQAs help foster a culture of quality and continuous improvement across departments. Their role is crucial in bridging the gap between routine laboratory work and compliance requirements.

What is Analytical Quality Assurance?

Analytical Quality Assurance (AQA) refers to the systematic processes and procedures implemented in laboratories to ensure the accuracy, reliability, and integrity of analytical test results. AQA involves method validation, instrument calibration, documentation, and adherence to regulatory guidelines. Its primary goal is to guarantee that analytical data meets required standards and supports decision-making in industries like pharmaceuticals, food safety, and environmental testing. Professionals in this field work to prevent errors and maintain compliance with quality standards such as Good Laboratory Practice (GLP) and ISO certifications.

What are the key skills and qualifications needed to thrive as an Analytical Quality Assurance professional, and why are they important?

To excel in Analytical Quality Assurance, you need a strong background in chemistry or life sciences, analytical testing methods, and familiarity with regulatory standards, usually supported by a relevant degree. Experience with laboratory information management systems (LIMS), chromatographic techniques (such as HPLC or GC), and certifications like ISO 9001 are commonly required. Attention to detail, critical thinking, and effective communication are important soft skills for ensuring data integrity and collaborating with cross-functional teams. These competencies are essential for maintaining product quality, regulatory compliance, and continuous process improvement in laboratory environments.

What jobs pay $500,000 a year in the US?

In the field of Analytical Quality Assurance, senior roles such as Director or Vice President of Quality often reach or exceed $500,000 annually, especially in large pharmaceutical or biotech companies. These positions typically require extensive experience, leadership skills, and advanced certifications, with compensation including base salary, bonuses, and stock options. High-level executive roles across industries can also surpass this threshold, but they are less common in entry-level or mid-tier positions.
More about Analytical Quality Assurance jobs
What states have the most Analytical Quality Assurance jobs? States with the most job openings for Analytical Quality Assurance jobs include:
What job categories do people searching Analytical Quality Assurance jobs look for? The top searched job categories for Analytical Quality Assurance jobs are:
Analytical Quality Assurance jobs near you
Infographic showing various Analytical Quality Assurance job openings in the United States as of July 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $93,338 per year, or $44.9 per hour.
Analytical QA Supervisor

Analytical QA Supervisor

Artius Solutions

Fall River, MA • On-site

$78K - $99K/wk

Full-time

Posted 11 days ago

Job description

Job Title: Analytical QA Supervisor
Location: Fall River, MA
Experience Required: 5 - 15 Years
Job Type: Full-time | On-site
Shift: General (8:30 AM – 5:00 PM; flexibility required as per business needs)
Reports To: QA Manager

Job Summary:
We are hiring an experienced Analytical Quality Assurance (QA) Supervisor to join our Quality team in Fall River. The ideal candidate will bring a strong analytical chemistry background, especially within a pharmaceutical manufacturing environment. This individual will ensure adherence to laboratory compliance standards and regulatory expectations while reviewing method validations, lab protocols, and raw data.

Key Responsibilities:

  • Oversee and verify method validation reports, comparisons, and study documentation.

  • Monitor laboratory operations for cGLP compliance and ensure SOPs are followed.

  • Review and assess standard operating procedures and test methods.

  • Support the review of process validation and characterization reports.

  • Coordinate with Regulatory and Lab teams for document readiness during ANDA submissions.

  • Maintain accurate records, track documents, and manage archival processes.

  • Review laboratory data, including audit trails, for compliance and accuracy.

  • Participate in laboratory incident investigations and drive CAPA implementations.

  • Review analytical documents for raw materials, in-process, and finished products.

  • Conduct internal audits and enforce lab compliance protocols.

  • Implement updates from Pharmacopoeial changes.

  • Handle assigned cross-functional projects as per business requirements.

Required Skills & Qualifications:

  • Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline (Master’s preferred).

  • 8–15 years of relevant experience in a regulated pharmaceutical QA environment.

  • Minimum 5 years specifically in Analytical QA roles within cGMP settings.

  • Strong understanding of analytical instrumentation: HPLC, UV Vis, GC, pH meters, stability chambers, etc.

  • Familiarity with USP monographs, FDA regulations, ICH guidelines.

  • Excellent documentation, communication, and investigation skills.

  • Hands-on experience with lab software, audit trails, and equipment calibration.

  • Exposure to dosage forms like MDI, solids, liquids, tablets, or capsules preferred.

  • Proficient in MS Office and quality management tools.

  • Must be fluent in English – verbal and written.

Additional Information:

  • On-site work only (remote not available).

  • Relocation assistance negotiable.

  • Weekend or holiday shifts may occasionally be required.

  • Compliance with PPE and cGMP environment standards mandatory.

Must Have:

  • Pharma industry experience (Bio-Pharma not acceptable)

  • Chemistry or relevant scientific background

  • QA experience in manufacturing & cGMP labs

  • Strong command of English