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Qa Incoming Inspector Jobs in Massachusetts (NOW HIRING)

Quality Assurance Manager

Salisbury, MA · On-site

$91K - $135K/yr

Manage and maintain the quality inspection and product release programs for a) incoming raw materials, b) in-process materials, c) components and d) finished goods * Set quality assurance objectives ...

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Qa Incoming Inspector information

How to become a QA Incoming Inspector?

To become a QA Incoming Inspector, candidates typically need a high school diploma or equivalent, along with experience in quality control or inspection roles. Relevant skills include attention to detail, knowledge of inspection tools and standards, and sometimes certifications like ASQ Certified Quality Inspector (CQI). Familiarity with industry-specific regulations and the ability to operate measurement instruments are also beneficial.

What are the key skills and qualifications needed to thrive as a QA Incoming Inspector?

To thrive as a QA Incoming Inspector, you need a solid understanding of quality assurance principles, inspection techniques, and familiarity with industry standards, often supported by a high school diploma or technical certification. Experience with measurement tools, ERP systems, and quality control software is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for accurately identifying and reporting defects. These skills ensure only compliant materials enter production, safeguarding product quality and organizational reputation.

What is a QA Incoming Inspector?

QA Incoming Inspectors are quality assurance professionals responsible for inspecting and verifying the quality of materials, parts, or products received from suppliers before they are used in manufacturing or production processes. Their main duties include conducting visual and measurement inspections, documenting findings, and ensuring that incoming goods meet established specifications and standards. They help prevent defective or non-conforming materials from entering the production line, which is crucial for maintaining product quality and safety.

What is the difference between Qa Incoming Inspector vs Qa Quality Auditor?

AspectQa Incoming InspectorQa Quality Auditor
CertificationsISO 9001, ASQ certifications often preferredISO 9001, ASQ certifications often preferred
Work EnvironmentInspection of incoming materials at receiving docks or warehousesAuditing quality systems across departments or facilities
Employer & Industry UsageManufacturing, automotive, electronicsManufacturing, pharmaceuticals, food industry
Search & Comparison IntentDifferences in roles, responsibilities, and skillsComparison of quality assurance roles

The Qa Incoming Inspector primarily focuses on inspecting incoming materials to ensure quality before production. In contrast, the Qa Quality Auditor evaluates overall quality systems and processes across the organization. Both roles require similar certifications and are common in manufacturing industries, but their responsibilities differ in scope and focus.

What are some typical challenges faced by a QA Incoming Inspector and how can they be addressed?

QA Incoming Inspectors often encounter challenges such as handling large volumes of incoming materials, ensuring accurate documentation, and identifying non-conforming parts under tight deadlines. To address these, strong organizational skills, attention to detail, and effective communication with suppliers and internal teams are essential. Leveraging digital inspection tools and maintaining clear records can also streamline the process and reduce errors, leading to smoother operations and improved product quality.
What are popular job titles related to Qa Incoming Inspector jobs in Massachusetts? For Qa Incoming Inspector jobs in Massachusetts, the most frequently searched job titles are:
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What cities in Massachusetts are hiring for Qa Incoming Inspector jobs? Cities in Massachusetts with the most Qa Incoming Inspector job openings:
Infographic showing various Qa Incoming Inspector job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Quality Assurance Manager

Milliken & Company

Salisbury, MA • On-site

$91K - $135K/yr

Full-time

Posted 25 days ago


Milliken & Company rating

7.7

Company rating: 7.7 out of 10

Based on 35 frontline employees who took The Breakroom Quiz

14th of 61 rated fashion and textile manufacturers


Job description

Milliken & Company is a global manufacturing leader whose focus on materials science delivers tomorrow's breakthroughs today. From industry-leading molecules to sustainable innovations, Milliken creates products that enhance people's lives and deliver solutions for its customers and communities. Drawing on thousands of patents and a portfolio with applications across the textile, flooring, chemical and healthcare businesses, the company harnesses a shared sense of integrity and excellence to positively impact the world for generations. Discover more about Milliken's curious minds and inspired solutions at Milliken.com and on Facebook, Instagram and LinkedIn.
POSITION TITLE / LOCATION: Quality Assurance Manager, Salisbury, MA
JOB CLASSIFICATION: Exempt
POSITION REPORTS TO: Director of Quality & Regulatory Assurance
POSITION OVERVIEW
The individual in this position will be part of a dynamic team with a proven track record of inventing, developing, and commercializing FDA registered medical devices. In this role the individual will interact with all functional areas of Ovik Health at our Mayflower Plant in Salisbury, MA. The associate will oversee the following as well as other duties as requested:
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
Quality Systems
  • Develop, implement, communicate and maintain effectiveness of a quality system that is in compliance with FDA QSR and ISO 13485 standards
  • Liaison with ISO 13485 registrar to ensure activities are completed in order to maintain ISO 13485 registration
  • Manage and maintain the quality inspection and product release programs for a) incoming raw materials, b) in-process materials, c) components and d) finished goods
  • Set quality assurance objectives for the review and approval of Top Management and ensure that targets are achieved
  • Establish and maintain appropriate controls and documentation procedures
  • Participate in new product development activities to ensure proper quality assurance and control plans can be implemented prior to beginning manufacturing
  • Support an effective supplier quality assurance system while ensuring supplier corrective actions are timely and effective
  • Implement new inspection, measurement and testing systems for quality monitoring and improvement
  • Track and report significant quality deviations
  • Develop and maintain an effective quality systems training program for all appropriate business associates
  • Manage all audit activities including internal, external, supplier, and FDA audits.
  • Conduct Management Reviews on a regular basis for location of responsibility
  • Review and approve SPIs
  • Develop, edit, review and approve validation protocols and reports.
  • Provide employee development opportunities for direct reports
  • Act as Management Representative for location of responsibility
  • Own CAPA, NC, and Complaint programs for location of responsibility

MINIMUM QUALIFICATIONS
  • Strong verbal and written communications skills
  • 4+ years Quality Assurance experience including 2 + years of supervisory leadership
  • ISO and FDA Quality systems knowledge
  • Bachelor's Degree in Science or Management preferred
  • Medical Device manufacturing desirable

PREFERRED QUALIFICATIONS
  • Six Sigma Certification
  • ISO 13485:2016
  • ISO 19011:2018

PERSONAL PROTECTIVE EQUIPMENT USED:
  • Safety Eyewear
  • Steel Toe Safety Shoes
  • Hairnet
  • Cut resistant gloves, chemical gloves, etc. as needed

PHYSICAL REQUIREMENTS FREQUENCY, AMOUNT, OR DESCRIPTION
Standing: Ability to stand while working: 60% of day
Sitting: Ability to sit down: 40% of day
Moving: Ability to move throughout plant: 100% of day
Lifting: Ability to lift to 25 lbs.: 100% of day
Ascending/Descending: Ability to walk upstairs, climb to top of range (approx. 16 ft): 50% of day.
Push/Pull/Reach: Ability to push/pull/reach: 5% of day
Bending: Ability to pick up objects from the floor 25% of day
Visual Acuity: Visual acuity adequate to perform job duties, including reading information from printed sources and computer screens. : 100% of day
Cognitive: Alert. Able to make decisions, reason, and understand information. : 100% of day
WORK ENVIRONMENT/SAFETY-SENSITIVE POSITION
This job operates in a manufacturing facility. This position is a safety-sensitive position and occasionally works around moving mechanical parts and powered industrial vehicles. Noise level can be medium to loud. Temperatures can vary depending upon the time of year and outside impacts.
Pay Transparency:
The salary range for this position is $91,500.00 to $135,000.00; the exact range depends on several factors such as experience, skills, education and budget.
Milliken is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, sex or gender (including pregnancy, childbirth or related medical condition, including but not limited to lactation), sexual orientation, gender identity or gender expression (including transgender status), ancestry, national origin, citizenship, age physical or mental disability, genetic information, marital status, veteran or military status or any other characteristic protected by applicable law.
To request a reasonable accommodation to complete a job application, pre-employment testing, a job interview, or to otherwise participate in the hiring process, please contact TalentAcquisition@milliken.com.
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