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Quality Associate Jobs in Maynard, MA (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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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for quality associate in Maynard, MA is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $33.27 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 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.

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 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.

More about Quality Associate jobs
What are the most commonly searched types of Quality jobs in Maynard, MA? The most popular types of Quality jobs in Maynard, MA are:
What job categories do people searching Quality Associate jobs in Maynard, MA look for? The top searched job categories for Quality Associate jobs in Maynard, MA are:
What cities near Maynard, MA are hiring for Quality Associate jobs? Cities near Maynard, MA with the most Quality Associate job openings:
Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Maynard, MA as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $59,220 per year, or $28.5 per hour.

Analytical Quality Assurance, Associate Director

Vertex Pharmaceuticals

Boston, MA • On-site

$156K - $234K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical

Job description

Job Description
General Summary:
The Associate Director (AD) Quality Assurance (QA for QC) is an advanced technical resource in the principles and application of quality assurance and compliance. This role is responsible for the quality oversight of Quality Control and analytical development activities of Cell & Gene programs. Activities in scope of this role include release analytical testing, stability testing, and QA support for deviations and out of specification investigations. The role will have QA oversight of technical analytical method validations and analytical transfer activities internally /CDMOs through the program life cycle management.
Key Duties and Responsibilities:
Analytical Lifecycle Management:
  • Serve as a Quality Assurance Subject Matter Expert for in QC domain and drive culture of quality to assure compliance with FDA, EMA, and internal SOPs.
  • Lead QA review and approval of analytical development, qualification and validation as well as analytical technical transfer activities
  • Ensure stability program is conducted in compliance with established protocols and applicable regulations.
  • Review relevant sections of regulatory submissions; Assist in responses to regulatory questions.

Compliance & Investigations
  • Ensuring proper root cause analysis (RCA) and Corrective and Preventive Actions (CAPA) for Out of Specification (OOS) and Out of Trend (OOT) results
  • Perform/lead QA review and approval of QC associated documentation including deviation investigations, OOS, OOT and change control.

CTO & CMO Management:
  • Execute QA operational oversight for internal QC laboratories and external contract testing laboratories.
  • Drafts and enforces Quality Agreements between Contract Test Labs and Vertex.

Digital & Artificial Intelligence
  • Demonstrated understanding of digital quality systems, data management, automation, and emerging AI technologies within regulated GxP environments.
  • Experience leveraging data analytics, digital tools, and AI-enabled solutions to improve quality oversight, operational efficiency, and decision-making.
  • Responsible for using platforms such as MES, LIMS, eQMS, data visualization tools, and advanced analytics to perform Quality oversight.

Quality Management Systems (QMS): Utilizing eQMS platforms for change controls and deviation tracking
  • Acting as the subject matter expert (SME) during audits and inspections regulatory agencies
  • Support/lead QA risk management activities, including mitigation plans and associated execution.
  • Support development of Vertex quality systems and processes, draft/revise SOPs, policies and work instructions.
  • Identify, facilitate, and/or lead continuous improvement efforts
  • Ensure development of quality metrics at the contract organizations that support excellence in quality systems

Knowledge and Skills:
  • In-depth global regulatory agency and technical knowledge and experience across GXP QA and QC activities in cell therapies
  • Broad understanding of regulatory environment including quality systems, compliance and GMP regulations.
  • Experience with platforms such as MES, LIMS, eQMS, data visualization tools, and advanced analytics is preferred.
  • Prior experience working /running internal analytical lab and working with external Test labs.
  • Experience in analytical method development
  • Ability to lead improvement projects - experience with Root Cause Analysis, data analytics, and other Operational Excellence experience, such as LEAN, DMAIC, Six Sigma.
  • Excellent communication skills and a proven track record Influencing/building/promoting a culture of Quality and Excellence.
  • Critical Thinking and Problem Solving skills

Education and Experience:
  • Master's degree in a scientific or allied health field (or equivalent degree)
  • Ph.D. preferred
  • 8+ years of experience, or the equivalent combination of education and experience in a regulated pharmaceutical environment.

Other Requirements:
  • Up to 15% travel

Pay Range:
$156,600 - $234,800
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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