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Quality Associate Jobs in Pelham, NH (NOW HIRING)

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Assoc Quality Inspector

Wilmington, MA

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Olema Oncology

Associate Director, GMP Quality

Boston, MA · On-site

$160K - $180K/yr

About the Role >>> Associate Director GMP Quality As the Associate Director, GMP Quality, reporting to the Head of GMP Quality, you will be responsible for oversight of GMP activities pertaining to ...

Textron

Assoc Quality Inspector

Wilmington, MA

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Textron

Assoc Quality Inspector

Wilmington, MA · On-site

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

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All JobsQuality Associate JobsQuality Associate Jobs in Pelham, NH

Quality Associate information

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$52

How much do quality associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality associate in Pelham, NH is $28.00, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $32.74 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the key skills and qualifications needed to thrive as a quality associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Pelham, NH?

The most popular types of Quality jobs in Pelham, NH are:

What cities near Pelham, NH are hiring for Quality Associate jobs?

Cities near Pelham, NH with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Pelham, NH as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $58,245 per year, or $28 per hour.

Research Associate II, Quality Control

Ocular Therapeutix

Bedford, MA

Full-time

Re-posted 13 days ago

Job description

Position Summary:

As a Research Associate II, your main task will be executing routine Quality Control (QC) testing activities as assigned. This position will support CAPA's, change controls, investigations, and deviations and participate in the development and validation of analytical methods for the Analytical Development group. You will also participate in testing, project support, data review, ordering of laboratory supplies, and general upkeep of the laboratory. 

Principal Duties and Responsibilities:

  • Support QC analytical chemistry testing using laboratory equipment and instrumentation (HPLC, UPLC, GC, KF, Dissolution etc).
  • Author technical reports as required.
  • Ensure instrument calibration and qualification is up to date and performed on a scheduled basis.
  • Troubleshoot any issues with instrumentation and coordinate repair with vendors as necessary.
  • Coordinate with Supervisor on scheduling of testing for reagents and product samples.
  • Participate in data review.
  • Participate in method development and validation activities
  • Coordinate external outsourcing of testing.
  • Support CAPA, change controls, investigations, and deviations and the timely closure of these items with Quality Assurance.
  • Follow Good Documentation Practices (GDP), maintaining contemporaneous records, filling out logbooks, forms, etc.
  • Adherence to cGMPs at all times.

Requirements:

  • Bachelor's degree in Chemistry or related field
  • 2+ years of work experience in a GMP Quality Control environment
  • Prior experience with HPLC and UPLC
  • Knowledge of CFR 210,211, USP and FDA/ICH guidance is preferred
  • Knowledge of safe laboratory practices
  • Strong verbal and written communication skills
  • Experience with USP App IV dissolution apparatus is preferred

Working Conditions:

  • Mix of office and laboratory environments.
  • Must be able to work in chemical laboratory environments.

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