Quality Inspection Specialist Job at MillenniumSoft Inc (Mannford)

Quality Specialist

We are seeking a dedicated Quality Specialist with experience in performing ship...

Location

United States , Houma

Salary:

Not provided

BOLLINGER MISSISSIPPI SHIPBUILDING LLC

Expiration Date

Until further notice

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

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

Competitive Pay
Comprehensive Benefits Package
Pay for Skills
Career Development
Cutting-Edge Projects
Positive Work Environment & Company Values

Quality Assurance Specialist

We are looking for a meticulous and technically skilled Quality Assurance Inspec...

Location

United Kingdom , Burgess Hill

Salary:

38000.00 - 42000.00 GBP / Year ▼

Office Angels

Expiration Date

Until further notice

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

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

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

Supplier Quality Specialist

Join our globally growing team at ATS Industrial Automation where we create comp...

Location

Canada , Cambridge

Salary:

Not provided

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

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

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

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

Qa quality specialist

This position reports to the Associate Director, External Quality, Quality Syste...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

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

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

Quality Systems Specialist

The Baxter Healthcare Ltd Compounding Facility in Dublin operates to a Manufactu...

Location

Ireland , Dublin

Salary:

Not provided

Baxter

Expiration Date

Until further notice

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

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

Pension
Health Insurance
Life Assurance
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Quality Specialist

As a Quality Specialist, you will play a central role in managing the food safet...

Location

Belgium , Antwerp

Salary:

Not provided

AXEREAL SCA

Expiration Date

Until further notice

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

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

Attractive salary and benefits package
Career opportunities internationally
Focus on flexibility, inclusion, collaboration and health and wellbeing

Fulltime

Center Quality Specialist

Essential Job Responsibilities and Duties and Qualifications

Location

United States , Fort Pierce

Salary:

Not provided

Assessfirst

Expiration Date

Until further notice

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

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

Quality Assurance Specialist - Warehouse/Supply chain

Join a global leader in Burgess Hill, supporting their warehouse and inspection ...

Location

United Kingdom , Burgess Hill

Salary:

18.94 - 21.73 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Experience in quality assurance or inspection within aerospace or automotive or manufacturing environments
Strong understanding of supply chain processes / root cause analysis
Confidence using systems such as SAP or similar ERP tools
A proactive mindset focused on continuous improvement and problem-solving

Job Responsibility

Investigate recurring quality issues with incoming parts
Engage directly with suppliers to understand root causes of non-conformance
Analyse inspection results and determine whether issues stem from the parts, the process, or the system
Review and improve inspection procedures to ensure accuracy and consistency
Collaborate with internal teams to ensure quality standards are upheld across the supply chain
Use systems like SAP to track quality data, supplier performance, and inspection outcomes

Fulltime

Quality Inspection Specialist

MillenniumSoft Inc

Location:
United States , Mannford

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 11, 2026

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Quality Inspection Specialist

MillenniumSoft Inc

Location:United States , Mannford

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 11, 2026

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Job Posted:
January 11, 2026