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Quality Engineer Associate Jobs in Lynn, MA (NOW HIRING)

Globus Medical

Associate Quality Engineer

Methuen, MA · On-site

The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies ...

Globusmedical

Associate Quality Engineer

Methuen, MA

The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies ...

Orion Castings

Quality Engineer

Billerica, MA · On-site

$64K - $86K/yr

Quality Engineer - 1st Shift The Quality Engineer oversees all Quality Assurance functions at the ... associates to corporate senior leadership. * Software Proficiency: Must be proficient with ...

Orion Castings

Quality Engineer

Billerica, MA · On-site

$64K - $86K/yr

Quality Engineer - 1st Shift The Quality Engineer oversees all Quality Assurance functions at the ... associates to corporate senior leadership. * Software Proficiency: Must be proficient with ...

Freudenberg Group

Quality Engineer I

Beverly, MA · On-site

$79K - $102K/yr

Minimum of 3 years of experience as a Quality Engineer * Minimum of 3 years of experience in a ... Employment opportunities are available to all applicants and associates without regard to race ...

Freudenberg

Quality Engineer I

Beverly, MA

$79K - $102K/yr

Minimum of 3 years of experience as a Quality Engineer * Minimum of 3 years of experience in a ... Employment opportunities are available to all applicants and associates without regard to race ...

Freudenberg Group

Quality Engineer II

Beverly, MA · On-site

$87K - $105K/yr

... Quality, Engineering, Operations, and customers, to drive problem-solving and continuous ... Employment opportunities are available to all applicants and associates without regard to race ...

Freudenberg

Quality Engineer II

Beverly, MA · On-site

$87K - $105K/yr

... Quality, Engineering, Operations, and customers, to drive problem-solving and continuous ... Employment opportunities are available to all applicants and associates without regard to race ...

New

Adecco

Senior Quality Engineer

Chelmsford, MA

$100K - $120K/yr

Adecco is hiring for a Sr Quality Engineer for a manufacturer in Devens! This is a direct hire ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Podimetrics

Quality Associate

Somerville, MA · On-site

Director, Quality and Regulatory Key Relationships: Sr. Quality Engineer, Device Operations ... The Quality Associate will work closely with Regulatory Affairs, Quality Engineering, Device ...

Podimetrics

Quality Associate

Somerville, MA

Director, Quality and Regulatory Key Relationships: Sr. Quality Engineer, Device Operations ... The Quality Associate will work closely with Regulatory Affairs, Quality Engineering, Device ...

SharkNinja

Senior Quality Engineer

Needham, MA · On-site

$96K - $130K/yr

Headquartered in Needham, Massachusetts with more than 4,100 associates, the company's products are ... Bachelor's Degree (or equivalent experience) in mechanical engineering, quality, product ...

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All JobsQuality Engineer Associate JobsQuality Engineer Associate Jobs in Lynn, MA

Quality Engineer Associate information

See Lynn, MA salary details

$17

$33

$50

How much do quality engineer associate jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for quality engineer associate in Lynn, MA is $33.56, according to ZipRecruiter salary data. Most workers in this role earn between $26.78 and $38.65 per hour, depending on experience, location, and employer.

What does a quality engineer associate do?

A Quality Engineer Associate supports the quality assurance and control processes within manufacturing or production environments. Their responsibilities typically include inspecting products, monitoring production processes, assisting with quality audits, and helping to implement quality standards and procedures. They work closely with senior quality engineers and production teams to identify defects, resolve quality issues, and ensure that products meet required specifications. This entry-level role is a great starting point for a career in quality engineering, as it provides hands-on experience with quality systems and tools.

What are some common challenges a quality engineer associate might face in their daily work?

Quality Engineer Associates often encounter challenges such as balancing multiple projects with tight deadlines, interpreting complex product specifications, and effectively communicating quality standards to cross-functional teams. They may also need to troubleshoot unexpected production issues and adapt quickly to new processes or technologies. Developing strong analytical and problem-solving skills, as well as building collaborative relationships with manufacturing, engineering, and quality assurance teams, can help overcome these challenges.

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

To thrive as a Quality Engineer Associate, you need a solid understanding of quality control principles, data analysis, and basic engineering concepts, usually supported by a bachelor’s degree in engineering or a related field. Familiarity with tools such as statistical process control (SPC), Six Sigma methodologies, and quality management systems (QMS) is often required, and certifications like ASQ CQE can be beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help you collaborate across teams and address quality issues proactively. These skills are vital for ensuring product reliability, compliance with standards, and continuous improvement in manufacturing or service processes.

What is the difference between Quality Engineer Associate vs Quality Technician?

AspectQuality Engineer AssociateQuality Technician
CredentialsTypically requires a bachelor's degree in engineering or related field; certifications like ASQ CQE are a plusUsually requires a high school diploma or associate degree; certifications like CQI or CQT are common
Work EnvironmentInvolves analysis, process improvement, and collaboration with engineering teamsFocuses on inspection, testing, and data collection on the production floor
Employer & Industry UsageUsed across manufacturing, aerospace, automotive, and electronics industriesCommonly employed in manufacturing and production settings

The Quality Engineer Associate and Quality Technician roles share a focus on quality assurance but differ mainly in responsibilities and required education. The associate typically engages in process analysis and improvement, while the technician concentrates on testing and inspection tasks. Both roles are vital in maintaining product quality within manufacturing industries.

Are quality engineer associates paid well?

Quality engineer associates typically earn competitive salaries that vary based on experience, location, and industry. Entry-level positions may start lower, but with skills in quality management tools and certifications, salaries can increase significantly over time.

Is a Quality Engineer Associate an entry level job?

A Quality Engineer Associate is typically considered an entry-level position in quality assurance and engineering. It often requires basic knowledge of quality tools, inspection processes, and sometimes certifications like Six Sigma Green Belt, making it suitable for those starting their careers in quality roles.

What cities near Lynn, MA are hiring for Quality Engineer Associate jobs?

Cities near Lynn, MA with the most Quality Engineer Associate job openings:

Quality Engineer Associate jobs near you
Infographic showing various Quality Engineer Associate job openings in Lynn, MA 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 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $69,812 per year, or $33.6 per hour.

Associate Quality Engineer

Globus Medical

Methuen, MA • On-site

Full-time

Re-posted 13 days ago

Globus Medical rating

6.7

Company rating: 6.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

444th of 545 rated manufacturers

Job description

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Position Summary:
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining and improving the quality management system, product quality, and manufacturing process quality.
Essential Functions:
  • Provide real-time quality support to manufacturing operations. Assist in identifying defects, performing root-cause analysis, and implementing corrections/corrective actions. Support defect reduction initiatives and process capability improvements.
  • Lead the containment, risk-based evaluation, disposition, and closure of Nonconforming Material records to prevent production delays and ensure consistent product quality
  • Facilitate MRB (Material Review Board) activities by preparing data, coordinating cross-functional input, and ensuring timely documentation
  • Drive continuous improvement in nonconforming material workflows, cycle time, and data accuracy
  • Support timely execution of CAPAs, ensuring proper documentation, risk assessment, and effectiveness verification. Collaborate with cross-functional teams to maintain CAPA compliance and prevent recurrence of issues.
  • Supports the development, implementation, and improvement of production monitoring methods and systems for product inspection and testing
  • Performs measurement systems analysis
  • Conduct thorough review of documentation, including but not limited to Document Change Orders (DCOs), engineering drawings, specifications, risk management files, and Verification & Validation (V&V) protocols and reports. Ensure documents meet regulatory, procedural, and quality system requirements and reflect appropriate risk controls and traceability.
  • Supports the validation of manufacturing processes, including activities associated with equipment installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ)
  • Assess Supplier documentation, including Certificates of Conformance, First Article Inspections, supplier process validations, quality agreements, and supplier responses to SCARs. Ensure suppliers provide adequate objective evidence and that documentation aligns with material, component, and product requirements.
  • Verify that all documentation changes are properly justified, risk-assessed, and approved through the appropriate change control process
  • Collaborate with cross-functional partners-Product Development, Operations, Supply Chain, Regulatory and Field Service-to clarify requirements, close gaps, and drive timely approval of documentation packages
  • Assist in preparation for external and internal audits by organizing documentation, gathering objective evidence, and responding to auditor requests. Support timely closure of audit observations.
  • Utilizes concepts of probability and statistical quality control to guide decisions
  • Establishes, follows, and improves company procedures
  • Provides written and oral reports to supervisor or other management personnel to keep them informed of activities and results. Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies. Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
  • Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Qualifications:
  • Bachelor's Degree required (science or engineering preferred)
  • 0-2 years' experience in quality assurance; experience in the medical device industry preferred
  • GMP and ISO experience
  • Strong proficiency in MS Office with knowledge of statistical analysis tools
  • Knowledge of Lean Manufacturing, Six Sigma, and reliability engineering is a plus
  • Must be a team player capable of working in a deadline dictated environment
  • Excellent verbal and written communication skills
  • Self-starter
  • Advanced critical thinking and problems-solving skills

Physical Demands:
The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
  • Required to sit; climb or balance; and stoop, kneel, crouch or crawl
  • Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
  • Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus

Our Values:
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
  • Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
  • Customer Focused: We listen to our customers' needs and respond with a sense of urgency.
  • Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
  • Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.

Equal Employment Opportunity:
Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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