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Analytical Quality Manager Jobs (NOW HIRING)

Analytical QA Supervisor

Fall River, MA ยท On-site

$78K - $99K/wk

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 ...

This position will report to the Quality Manager . Job Scope The Analytical Quality Chemist is responsible for supporting the Conroe manufacturing site through quality systems leadership, analytical ...

Quality Manager Location: McGregor, Texas Department: Quality Reports To: Plant Manager Join ... analysis, quality assurance methodologies, auditing processes, and continuous improvement ...

Identify, analyze, and develop improvements in throughput, productivity, quality, client ... Manage annual AS9100 certification surveillance or recertification audits. * Continuous reporting ...

Lead and manage all plant quality functions, including Quality Engineers, Technicians, and lab ... Monitor KPIs, analyze quality performance, and implement corrective and preventive actions

Quality Manager

San Antonio, TX ยท On-site

$100K/yr

Develop, monitor, and report Quality KPIs to senior management on a routine basis. * Analyse quality trends and provide recommendations for improvement * Prepare and present quality performance ...

Develop, monitor, and report Quality KPIs to senior management on a routine basis. * Analyse quality trends and provide recommendations for improvement * Prepare and present quality performance ...

... and analyze quality metrics, identify areas for improvement, and implement corrective and ... and manage documentation for quality reports, audits, and regulatory submissions. - Lead ...

Quality Manager Full Time Management Georgetown, TX, US Quality Manager Total Site Solutions ... Analyze quality data and generate reports to support decision-making and continuous improvement.

Quality Manager Total Site Solutions, Georgetown, TX. , is seeking a detail-oriented Quality ... Analyze quality data and generate reports to support decision-making and continuous improvement.

Identify, analyze, and develop improvements in throughput, productivity, quality, client ... Manage annual AS9100 certification surveillance or recertification audits. * Continuous reporting ...

Develop, monitor, and report Quality KPIs to senior management on a routine basis. * Analyse quality trends and provide recommendations for improvement * Prepare and present quality performance ...

Quality Manager

Big Rapids, MI ยท On-site

$130K - $150K/yr

Quality Manager - Automotive Manufacturing Position Overview We are seeking an experienced ... Develop and analyze quality data to identify trends, prevent recurring issues, and improve plant ...

Conduct root cause analysis using methodologies such as 8D, 5 Why, Fishbone, and Pareto analysis ... Manage supplier quality performance, audits, corrective actions, and scorecards. * Support incoming ...

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How much do analytical quality manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for analytical quality manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

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Cities with the most Analytical Quality Manager job openings:

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Infographic showing various Analytical Quality Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Analytical QA Supervisor

Fall River, MA โ€ข On-site

Artius Solutions
Recruiting and Staffing Servicesย โ€ขย 11 - 50 employees

$78K - $99K/wk

Full-time

Re-posted 26 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