CrawlJobs Logo

Quality Inspection Specialist

gomillenniumsoft.com Logo

MillenniumSoft Inc

Location Icon

Location:
United States , Andover

Category Icon

Job Type Icon

Contract Type:
Employment contract

Salary Icon

Salary:

18.00 - 22.00 USD / Hour

Job Description:

Contract. Performs visual, dimensional and functional inspections on a wide variety of products in accordance with internal procedures and Product Specifications. Reports non-conformances to Supervisor and discusses corrective action. In addition, follows-up to see if corrective action was effective. Determines whether product is acceptable or rejected, initiates rejection notices, and maintains accurate written records of the inspections performed, including the results. Recognizes conditions outside their specific areas of inspection which require action and refers the items to the supervisor. Monitors compliance to G.M.P. in employee working areas and reports infractions to Q.C. Supervisor for corrective action. Employee evaluates both the product and process, making decisions on subjective visual inspections. Responsibilities have an impact on product quality, productivity, and product costs as affected by internal and external costs of rework, scrap and product warranty.

Job Responsibility:

  • Performs visual, dimensional and functional inspections on a wide variety of products in accordance with internal procedures and Product Specifications
  • Reports non-conformances to Supervisor and discusses corrective action
  • Determines whether product is acceptable or rejected, initiates rejection notices, and maintains accurate written records of the inspections performed
  • Recognizes conditions outside their specific areas of inspection which require action and refers the items to the supervisor
  • Monitors compliance to G.M.P. in employee working areas and reports infractions to Q.C. Supervisor for corrective action
  • Employee evaluates both the product and process, making decisions on subjective visual inspections.

Requirements:

  • Six (6) months related experience in a manufacturing environment preferred
  • High school diploma or GED
  • One to two (1-2) years related Quality Control experience or equivalency
  • Must be able to read and comprehend English
  • Ability to withstand repetitive motion and to lift up to 50 lbs.
  • Demonstrated human relation and communications skills.

Additional Information:

Job Posted:
January 11, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Quality Inspection Specialist

Quality Specialist

We are seeking a dedicated Quality Specialist with experience in performing ship...
Location
Location
United States , Houma
Salary
Salary:
Not provided
bollingershipyards.com Logo
BOLLINGER MISSISSIPPI SHIPBUILDING LLC
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience performing shipyard QA/QC functions OR 7 years of heavy manufacturing, craft experience (fitting/welding/paint/electrical/etc.), or shipyard related quality (testing/inspecting) experience
  • Strong understanding of quality assurance and control principles
  • Attention to detail and precision in inspection and testing tasks
  • Communicating procedures and processes in an effective manner
  • Effective communication skills, both written and verbal
  • Good problem-solving skills and ability to work independently or as part of a team
  • Proficiency in using standard software for documentation and reporting
  • Basic computer skills and proficiency in MS Outlook, Word, and Excel
Job Responsibility
Job Responsibility
  • Perform QA/QC functions to ensure compliance with industry standards and company requirements
  • Read inspection and test procedures, interpret codes, specifications, and advanced blueprints
  • Conduct inspections and tests according to established procedures
  • Follow written and verbal instructions accurately
  • Communicate procedures and processes effectively to team members
  • Utilize standard software (MS Outlook, Word, and Excel) for documentation and reporting
What we offer
What we offer
  • Competitive Pay
  • Comprehensive Benefits Package
  • Pay for Skills
  • Career Development
  • Cutting-Edge Projects
  • Positive Work Environment & Company Values
Read More
Arrow Right

Quality Assurance Specialist

We are looking for a meticulous and technically skilled Quality Assurance Inspec...
Location
Location
United Kingdom , Burgess Hill
Salary
Salary:
38000.00 - 42000.00 GBP / Year
https://www.office-angels.com Logo
Office Angels
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Completed technical training, apprenticeship, or equivalent in the aerospace or automotive industry
  • 2-4 years of experience in a similar quality assurance or inspection role
  • Proficient in using mechanical testing tools such as micrometers and calipers
  • Working knowledge of QA inspection methods and procedures
Job Responsibility
Job Responsibility
  • Perform dimensional and visual inspections in line with design specifications and Acceptable Quality Limits (AQL)
  • Verify product compliance and provide objective evidence of inspection results
  • Review certification documents to ensure traceability in accordance with AS9100 and Boeing quality standards
  • Conduct audits, surveillance, and monitoring activities to ensure ongoing compliance
  • Identify and document discrepancies, segregate non-conforming items, and support preliminary review and disposition
  • Participate in product reviews with customers during verification processes
  • Highlight recurring or significant non-conformances and initiate corrective action requests
  • Support the development of inspection plans and assist with internal, customer, and third-party audits
  • Complete internal and external online QA training courses as required
What we offer
What we offer
  • Eye care vouchers and money towards glasses should you require them for VDU purposes
  • Weekly pay
  • Pension scheme option (with employer contributions)
  • 28 days paid annual leave (Based on a weekly accrual)
  • Fulltime
Read More
Arrow Right

Supplier Quality Specialist

Join our globally growing team at ATS Industrial Automation where we create comp...
Location
Location
Canada , Cambridge
Salary
Salary:
Not provided
atsautomation.com Logo
ATS Automation Tooling Systems Inc.
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A post-secondary technology diploma or equivalent, specializing in toolmaking, machining, welding or mechanical engineering, mechanical technologist, quality engineering or equivalent work experience is required
  • ASQ CQE or ASQ SSBB or equivalent work experience is required
  • Nuclear Auditor training and qualification
  • At least 5 years in nuclear environment or other highly regulatory industry
  • At least 5 years of quality assurance engineering experience in a manufacturing and/or fabrication environment
  • Experience with the Nuclear requirements relating to Quality and Inspection plans
  • Demonstrated ability to work independently and to manage multiple projects from various diverse organizations
  • Strong working knowledge and experience working with ISO 9001, N299, NQA-1,10CFR50, 10CFR21, N285, N286, B51 and ASME Section III guidelines
  • Commercial Grade Dedication background and experience
  • Capable of being certified to Jaeger-1 Test Chart and Bausch and Lomb Vision test (including color and far- and near-distance test)
Job Responsibility
Job Responsibility
  • Lead the charge in sourcing and developing top tier suppliers, by providing expert guidance on technology, performance, quality, cost, logistics and delivery
  • Partner closely with engineering teams and suppliers to drive innovation while elevating process and quality standards
  • Monitor industry advancements and recommend technologies that enhance cost effectiveness, product quality, and supply chain reliability
  • Be a catalyst for change by actively contributing to ongoing continuous improvement initiatives
  • Work directly with suppliers to boost their quality output and shipping performance
  • Champion ABM initiatives
  • Conduct supplier audits to ensure full compliance with relevant industry standards and certifications (ISO 9001, CSA N299, CSA N285, NQA-1)
  • Strictly follow CSA N285/NQA Quality requirements as defined within the manual and procedures
  • Existing Supplier Development to improve KPI’s (e.g. OTD, Conformance to Specifications, Receiving issues)
  • Perform rough cut capacity planning and resolve gaps at ATS Approved Suppliers
What we offer
What we offer
  • Competitive starting salaries
  • comprehensive health and dental benefits
  • overtime pay
  • employee bonus
  • RSP matching
  • Employee Share Purchase Program
  • treat days
  • gourmet coffee and beverages
  • subsidized breakfast and lunches in our cafeteria
  • employee referral bonuses
  • Fulltime
Read More
Arrow Right

Qa quality specialist

This position reports to the Associate Director, External Quality, Quality Syste...
Location
Location
Ireland , Cork
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree in science or engineering
  • Minimum 3+ years of biopharmaceutical experience in a Quality, Compliance, and/or Regulatory setting
  • Skilled in data analysis and excel
  • Strong communication and interpersonal skills – Oral, written and presentation skills
  • Works collaboratively with others to meet shared objectives.
Job Responsibility
Job Responsibility
  • Perform the Quality Systems Metric Review for External Quality and oversee relevant metrics and trending for each quality system to proactively drive on-time closure of Quality records
  • Responsible for managing routine cross-functional meetings to ensure timely closure of Deviations, CAPAs and Change Control, with leadership endorsement
  • Responsible for development/reporting of metrics and supporting standardization of these across the Organization
  • Co-ordinate monthly governance site quality review team (SQRT) meeting for GEO / External Quality
  • Deliver training on Quality Management Systems, as required
  • Partner with the Global Quality Systems Management Team and other cross functional groups to ensure proper application of the QMS
  • Identify and implement continuous improvement initiatives to the External Quality systems
  • Assist as needed in audits and inspections
  • Participate in development and implementation of global alignment projects with BioMarin’s sister sites
  • Manage the Self Inspection Programme for External Quality
Read More
Arrow Right

Specialist Quality Engineer

The Senior Quality Engineer leads the execution of Quality activities for medium...
Location
Location
United States , Northampton
Salary
Salary:
Not provided
l3harris.com Logo
L3Harris
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree and minimum 4 years of prior relevant experience, or Graduate Degree and a minimum of 2 years of prior related experience. In lieu of a degree, a minimum of 8 years of directly related prior experience may be considered
  • Ability to obtain Secret level security clearance which requires US Citizenship
  • Subject matter expert in advanced problem solving (such as 8D, A3, DMAIC, RCCA)
  • Experience Leading and supporting FMEAs for process improvement and design
  • Strong proficiency in design reviews, drawing reviews, engineering change order incorporation
Job Responsibility
Job Responsibility
  • Evaluate and disposition customer returns, in-process defects, and address day to day quality concerns. Rapidly implementing containment and corrective actions as applicable
  • Support Quality leadership to ensure methodology is applied in a way that supports business performance and true alignment of business goals and objectives
  • Effectively communicate across multiple organizations to align a strategic and tactical path to success for manufacturing operations at the site while improving quality
  • Support, mentor, and guide cross-functional groups in problem solving efforts confirming root cause identification, generating corrective actions and verification items are implemented and sustained
  • Participate in the planning and implementation of the L3Harris Zero Defect Plan program
  • Generate and analyze data and metrics to prioritize corrective action and improvement activities
  • Participate in and support manufacturing (Gemba) and program status and scrum meetings
  • Plan, analyze, survey and control to assure that all applicable quality requirements are adhered to in all phases of a program, from initial proposal through end customer acceptance
  • Review new contracts to determine the quality assurance requirements and flow down requirements to the appropriate level
  • Participate in Engineering design reviews, review engineering drawings for conformance to quality requirements and sign off on approved drawings
Read More
Arrow Right

Quality Systems Specialist

The Baxter Healthcare Ltd Compounding Facility in Dublin operates to a Manufactu...
Location
Location
Ireland , Dublin
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree or equivalent experience in Science or related field
  • post qualification experience of at least 1 years in a GMP environment, ideally in a quality role
  • experience in dealing with Regulatory Compliance desired
  • good problem solving and investigation skills would be beneficial
  • an ability to work in a dynamic, fast-paced and goal driven environment
  • be dedicated
  • meticulous in attention to professional standards
  • good professional standards and demonstrates good attention to detail
  • ability to work under pressure and meet deadlines
  • highly motivated self-starter and team worker
Job Responsibility
Job Responsibility
  • Ensure the compilation of Quality Management Review process
  • review and approval of process change controls, SOPs, NCRs and CAPAs
  • implementation, execution and administration of Change Control System and NCR System
  • administration of Recall process with the Quality management team
  • administration/co-ordination of risk assessments
  • support facility projects including process development and quality improvement initiatives
  • manage and maintain the Documentation System
  • manage site archive, storage, retrieval and destruction processes
  • review and approval of Quality documentation
  • assist in the collation of information and preparation of reports for Annual Product reviews
What we offer
What we offer
  • Pension
  • Health Insurance
  • Life Assurance
  • Employee Health & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Quality Specialist

As a Quality Specialist, you will play a central role in managing the food safet...
Location
Location
Belgium , Antwerp
Salary
Salary:
Not provided
axereal.com Logo
AXEREAL SCA
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master/Bachelor Degree in a food science or related discipline, or equivalent in-role experience
  • Speak and write Dutch and English fluently
  • Experience in or passion for the food production sector, preferably malting or brewing
  • Relevant experience in quality, malting or brewing
  • Knowledge of HACCP, food safety and quality systems within the food or drinks industry (preferably FSSC 22000)
  • Think and work in an analytical and structured way
  • Strong sense of perseverance and follow up on issues until they are fully resolved
  • Like thinking out of the box and coming up with innovative ideas and solutions
  • Have a driver license
Job Responsibility
Job Responsibility
  • Support the Quality Manager to ensure that your sites comply with Group Quality, food and feed safety policies and standards
  • Prepare and own the internal audit and inspection plan for the sites within the cluster and provide support on external audits
  • Investigate non-conformities and implement preventive and corrective actions to ensure zero food safety incidents (from audits or customer complaints)
  • Provide relevant support and training in areas such as understanding Quality, food safety and hygiene and assist in management of relevant documentation
What we offer
What we offer
  • Attractive salary and benefits package
  • Career opportunities internationally
  • Focus on flexibility, inclusion, collaboration and health and wellbeing
  • Fulltime
Read More
Arrow Right

Center Quality Specialist

Essential Job Responsibilities and Duties and Qualifications
Location
Location
United States , Fort Pierce
Salary
Salary:
Not provided
assessfirst.com Logo
Assessfirst
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school diploma, GED or equivalent required
  • Associates degree preferred or a minimum of (3) three to (6) six months quality or plasma industry experience required
  • Strong verbal and written communication skills
  • Must have above average problem-solving and decision-making abilities
  • Proficiency with computers
  • Must have explicit attention to detail
  • Must have excellent analytical skills, organization skills, and follow-up
  • Ability to read and interpret documents such as safety rules, operating and maintenance instruction, and procedure and technical manuals
  • Ability to interpret a wide variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
  • Use hands to handle or feel objects, tools, or controls
Job Responsibility
Job Responsibility
  • Perform donor record file review
  • Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual
  • Review medical reports and communication
  • Perform reviews of equipment incidents
  • Verification and release of sample shipment
  • Responsible for the inspection and release of incoming supplies
  • Initiate deviation reports as needed
  • Perform Weekly employee observations
  • Assist the Manager of Quality Assurance with compliance of all state and federal regulations, FDA-approved Standard Operating Procedure Manual, Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP), Occupational Safety and Health Administration (OSHA), and internal company procedures
  • Reviews the documentation of unsuitable test results and the disposition of the associated units
  • Fulltime
Read More
Arrow Right