Quality Assurance Engineer - Critical Hardware
Quality assurance specialist job in Macomb, MI
Lincoln Electric is the world leader in the engineering, design, and manufacturing of advanced arc welding solutions, automated joining, assembly and cutting systems, plasma and oxy-fuel cutting equipment, and has a leading global position in brazing and soldering alloys. Lincoln is recognized as the Welding Expert™ for its leading materials science, software development, automation engineering, and application expertise, which advance customers' fabrication capabilities to help them build a better world. Headquartered in Cleveland, Ohio, Lincoln Electric is a $4.2B publicly traded company (NASDAQ:LECO) with over 12,000 employees around the world, with operations in 71 manufacturing and automation system integration locations across 21 countries and maintains a worldwide network of distributors and sales offices serving customers in over 160 countries.
Location: Macomb
Employment Status: Hourly Full-Time
Function: Quality Assurance/Control
Req ID: 26199
Job Responsibilities
PRIMARY FUNCTION
Quality Assurance is a vital part of any aerospace operation as it ensures that all operations are conducted in a safe and reliable manner. The candidate must be able to identify any potential issues or risks that could compromise safety, performance, or reliability and take appropriate corrective action. Experience in auditing, inspection, and testing procedures is essential for success in this role. Possessing these skills and qualifications, a Quality Assurance Engineer can help to ensure the highest quality standards are met here at Baker Industries.
JOB DUTIES AND RESPONSIBILITIES
Documenting and reporting product or service quality levels
Developing a workflow or AS9102 Form 3 for product inspection
Following up with the appropriate channels when mistakes are found
Evaluating adequacy of Quality Assurance standards
Devising sampling procedures and directions for recording and reporting quality data
Reviewing the implementation and efficiency of quality and inspections systems
Investigating customer complaints and non-conformance issues
Collecting and compiling statistical quality data
Analyzing data to identify areas for improvement in the quality system (Continuous Improvement)
Developing, recommending, and monitoring corrective and preventive actions
Preparing reports to communicate results of quality inspection activities to management
Monitoring risk management activities
Assuring ongoing compliance with quality and industry regulatory requirements
Prioritizing work and meeting deadlines
Recognizing and maintaining the confidentiality of all materials in the work setting.
Possessing a keen eye for detail with excellent attention to detail
The ability to consistently identify mistakes across thousands of inspections characteristics, closely follow International Quality Standards as well as customer requirements, read and interpret engineering drawings and specifications.
Use problem-solving skills to identify potential issues with a product and propose solutions to fix them.
Ability to effectively communicate with and work in teams. .
Additional job duties as assigned
EDUCATION AND EXPERIENCE
Proven work experience as a Quality Assurance Engineer or DSQR.
Relevant training, experience, and/or certifications as a Quality Assurance Engineer.
Experience with flight hardware is a must.
Working knowledge of AS9100, AS9102, AS13100, ISO 9001, and other relevant quality standards. Must have strong computer skills, including Microsoft Office and databases. Experience with DISCUS is a plus.
Working knowledge of tools, methods, and concepts of quality assurance.
High school diploma/GED, prior certification as a DSQR for any Aerospace Prime contractor, or equivalent work experience.
Job Requirements
PHYSICAL DEMANDS
The employee frequently is required to stand; walk; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. The employee is required frequently to work from ladders and scaffolds. The employee is occasionally required to sit. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EXPORT CONTROL DISCLAIMER
This position will include access to data, technology, and/or software source code that is subject to U.S. export controls under International Traffic in Arms Regulations (ITAR). Employment with The Lincoln Electric Company (D/B/A Baker Industries) is contingent upon either verifying U.S. person status or obtaining any necessary authorizations. Applicants will be required to answer certain questions for export control purposes and information will be reviewed by compliance personnel to ensure compliance with federal law. The Lincoln Electric Company, at its sole discretion, may choose not to apply for a license for such individuals as whose access to export-controlled data, technology, and/or software source code may require authorization. The Lincoln Electric Company may also decline to proceed with an applicant on this basis alone.
EQUAL OPPORTUNITY EMPLOYER
The Lincoln Electric Company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Baker Industries complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, protected veteran status, or disability.
HARASSMENT POLICY
The Lincoln Electric Company expressly prohibits any form of workplace harassment based on race, color, religion, gender, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Baker Industries' employees to perform their job duties may result in discipline up to and including discharge.
DISCLAIMER
This job description may not include all assigned duties, responsibilities, or aspects of the job described, and may be modified at any time at the Employer's sole discretion.
Lincoln Electric is an Equal Opportunity Employer. We are committed to promoting equal employment opportunity for applicants, without regard to their race, color, national origin, religion, sex (including pregnancy, childbirth, or related medical conditions, including, but not limited to, lactation), sexual orientation, gender identity, age, veteran status, disability, genetic information, and any other category protected by federal, state, or local law.
QA Engineer
Quality assurance specialist job in Sterling Heights, MI
We're seeking a QA Automation Engineer to design, develop, and maintain automated test coverage for our .NET and Angular applications.
This role focuses heavily on building end-to-end and API tests in Playwright, integrating them into our Woodpecker CI pipelines, and ensuring each pull request is validated through automated testing.
The ideal candidate will have experience scripting in TypeScript or JavaScript, working with REST APIs, and collaborating with developers to improve test reliability and system quality.
Responsibilities
Design, build, and maintain Playwright test suites for Angular front-end and .NET API validation.
Develop reusable test cases and automation frameworks for regression, smoke, and integration testing.
Integrate automated tests into the Woodpecker CI/CD pipeline, validating each PR and build.
Collaborate with developers to identify and automate high-value test cases early in development.
Maintain and extend existing manual and automated test case documentation.
Create test data and environment setup scripts for repeatable, isolated test runs.
Monitor pipeline test results, investigate failures, and report issues in Jira.
Continuously improve automation coverage, reporting, and stability of tests.
Work with existing QA members to elevate their skill set in the automation space.
Required Skills & Experience
3+ years of experience in QA automation or software testing.
Proficiency with Playwright (preferred) or similar tools (Cypress, Selenium, Puppeteer, Robot Framework).
Strong skills in TypeScript or JavaScript.
Experience testing REST APIs and validating request/response data.
Familiarity with CI/CD tools (Woodpecker CI, Jenkins, GitHub Actions, Drone, etc.).
Understanding of Git workflows, PR testing, and version control practices.
Experience authoring clear, maintainable test cases and automation scripts.
Basic understanding of .NET, Angular, and containerized environments (Podman/Docker).
Preferred Skills
Experience writing API test suites in Postman or Playwright's API module.
Knowledge of SQL for data validation and test verification.
Understanding of QA metrics, test coverage analysis, and reporting.
Soft Skills
Strong analytical and problem-solving ability.
Excellent communication and documentation skills.
Comfortable working closely with developers and DevOps engineers.
Proactive and detail-oriented, with a focus on improving test quality and speed.
Why Join
You'll be at the center of our automation initiative, building the test infrastructure that ensures every build, deployment, and PR meets our quality standards. You'll have the freedom to shape our automation strategy, develop Playwright frameworks, and directly impact how software moves from development to production.
Psychological Testing Specialist
Quality assurance specialist job in Flint, MI
$5,000 Signing Bonus!
Join a mission-driven clinical team providing high-quality psychological and neuropsychological assessments for children, adolescents, teens, and families. This role offers strong supervision, professional development, and a supportive clinic-based environment.
What You'll Do
Administer and score cognitive, developmental, behavioral, and neuropsychological tests
Use standardized methods and normative data to ensure accurate results
Prepare clear, timely written summaries
Collaborate with licensed Psychologists in diagnostics and care planning
What We're Looking For
Master's in Psychology
Michigan LLP (or TLLP with path to LLP after 2,000 hours)
1+ year experience working with children/adolescents with developmental, intellectual, or emotional/behavioral disorders
Must pass the EPPP within 4 years
Valid driver's license and reliable transportation
Software QA
Quality assurance specialist job in Southfield, MI
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Job Description
Position Details:
Title: QA Analyst
Location: Southfield, MI
Duration: 6 month (may extend)
Our top direct client is looking for a QA Analyst for a long term project in Southfield, MI
The client is a Fortune 50 multi-billion dollar revenue generating organization with a spectrum of products and services throughout major operating businesses.
Responsibilities:
Part of scrum team, Development of automation Testing and work with business and tech leaders.
Proactively develop the automation within process and work with Dev closely.
Support any production issues as needed
Must Have(s):
QTP
Selenium
SOAP UI
Automation Experience
Additional Information
Please contact:
Monil Narayan
************
monil.narayan(@)collabera.com
Quality Assurance Specialist
Quality assurance specialist job in Detroit, MI
Job Description
Employment Type: Contract Role (1099)
About Us
Were a fast-growing startup operating in specialized alternative markets, where every detail matters. Our team is small, agile, and focused on building operations that are reliable, disciplined, and scalable. Were looking for someone who takes pride in precision, thrives in structured environments, and enjoys ensuring that systems and processes perform exactly as intended.
About the Role
As a Quality Assurance Specialist, youll serve as the checkpoint for accuracy and consistency across our workflows. Youll verify execution against SOPs, identify anomalies, and escalate issues that need higher-level resolution. This role is ideal for someone who finds satisfaction in getting it right, keeping meticulous records, and ensuring operational processes run to standard every single time.
Key Responsibilities
Verify workflows and task completion against established SOPs
Conduct pre- and post-execution checks to confirm accuracy
Identify irregularities or edge cases and escalate appropriately
Maintain complete and transparent documentation of actions and outcomes
Perform field-based verifications or client-specific checks (local travel required)
Who You Are
Accuracy-Focused: You notice discrepancies others miss and take pride in clean, correct work.
Process-Disciplined: You work best with structured checklists and defined procedures.
Calm & Reliable: You perform steadily in live, time-sensitive environments.
Tech-Literate: You can comfortably navigate platforms, dashboards, and browser-based tools.
Locally Available: Youre based in the Detroit metro area (or open to relocating) and can handle daily travel as needed.
Bonus Points
Experience in QA, compliance, lab testing, auditing, or other structured review environments
Familiarity with high-precision, SOP-driven work
Exposure to both digital and in-person verification tasks
Achievement in competitive video games or strategy games
New grads and new workers welcome
Why Join Us
Competitive hourly pay with additional performance incentives
A structured environment with clear expectations and reliable workflows
Direct impact on maintaining the precision and trustworthiness of a fast-growing startup
Well-documented SOPs and strong team collaboration so you can work with confidence
Quality System Specialist
Quality assurance specialist job in Southfield, MI
Support to the development, implementation and Continual Improvement of the global Quality Management System and related Business Process.
Perform proper internal audits as for defined audit plan.
Support the monitoring of Quality KPIs.
Support the monitoring of milestones execution (QAMM)
Duties and Responsibilities
(these are the positions essential duties and is not an all-inclusive list)
Main areas of responsibilities are:
Participate in the development of the Global Quality Management System based on Business Processes and their continuous improvement.
Perform internal audits that measure the effectiveness of the Systems as for defined audit plan.
Maintain Quality Management System documentation updated according to guidelines.
Support the monitoring of Quality KPIs, the analysis of results and the monitoring of improvement plans.
Support the monitoring of milestones execution (QAMM), the analysis of results and the monitoring of improvement plans.
Support continuous improvement activities e.g., Kaizen, 5S, Six Sigma projects, value engineering, lean manufacturing, etc.
Controls Assurance Auditor
Quality assurance specialist job in Auburn Hills, MI
The Controls Assurance Auditor will support in the scoping, planning, creation and execution of testing of internal controls over financial reporting (“ICFR”) based on the assessment approach to assess the design and operating effectiveness. In addition, this role will involve coordination of test schedule and procedures with the control owners and internal as well as external auditors, as needed. The Controls Assurance Auditor will conduct walkthrough meetings with control owners, execute the entire testing cycle through fieldwork and reporting of the assigned audit areas. The Auditor will perform the assigned test plan consistently with the guidance received and based on the feedback received by the manager during the engagement. The Auditor will also communicate the status and results of ICFR testing procedures to the control owners and will support the team in the communication to other various stakeholders including management and external auditors.
Additional responsibilities include:
Assist with overall scoping and planning procedures for the assessment cycle
Effectively contribute to process improvement initiatives across the organization
Support the development of the audit plan and testing approach
Execute test plans, procedures and processes of business areas' test programs against the testing standards
Create accurate, logical and detailed work papers clearly describing the work performed, results of testing and conclusions reached
Validate accuracy and alignment of relevant ICFR documentation (i.e.: control descriptions, risk/control matrices, mapping of controls to financial statement assertions, etc.)
Create, maintain and revise internal control documentation
Maintain a project plan, which ensures timely completion of ICFR testing in compliance with internal/external audit requirements and deadlines
Provide ongoing testing status updates to team
Support the management of Governance, Risk and Compliance (“GRC“) system maintenance and usage
Coordinate test schedule and procedures with the external auditors and management
Identify and escalate risk exposures to appropriate levels of management
Prepare deficiency language for issues identified during testing procedures and effectively communicate to control owners
Work with the manager in formal written reports to management summarizing audit results
Execute special projects, as assigned
What You'll Learn:
Understand business processes from the initiation of activity through recording, the related controls and risks
Identify potential gaps in risks and controls within the control framework presenting potential exposure to management
Conduct with different levels of management including interviews to perform testing, learn business processes, provide status updates and deliver issues
Perform testing over multiple business processes
Writing skills to document processes and testing procedures
Document deficiency language and appropriately communicating the issues to control owners
Active participation to the team assigned to the audit
Present testing status and communicate issues noted
Assist in preparing reports and presentations to top management
Build relationships with the control owners
Work with other testing teams from different countries to ensure consistency in testing and process documentation
What This Role Will Prepare You For:
Roles (including manager roles) within Group Controls Assurance, Internal Controls and Financial Reporting, Corporate Finance and Corporate Accounting
Primary Metallurgical QA Professional II
Quality assurance specialist job in Canton, MI
Joining the Metallus team means becoming part of a legacy that dates back over a century. We are an industry leader, manufacturing the cleanest steel in the world for companies in the industrial, aerospace and defense, automotive, and energy markets.
Relocation will not be offered for this position.
Purpose
This position exists to provide expert level metallurgical knowledge to direct the chemical and testing application aspects of primary steelmaking for bar products and piercing mill billets. In this position the Primary Metallurgical QA Professional has technical oversight for the metallurgical process defined on every product. This position is responsible to ensure that every heat has a process route that satisfies a customer order/requirement, process review is performed, and nonconformance testing is added as needed according to standard 6.02.10. Production scheduling is performed so the individual operations are optimized based on shop conditions. Required to work rotating shift, overtime, and weekends as per business needs.
Responsibilities
* Audit to ensure that hourly associates follow standard manufacturing processes, provide direction to melt shop supervision and hourly associates, answer questions, and offer guidance during unusual situations. Evaluate final chemistry and determine if heats meet customer requirements. Rate heats based on standards 42.09.01, 06.02.10, 06.01.03, work order requirements and Metallus mill order requirements.
* Responsible to document manufacturing processes nonconformances (Class 9 events) and actions taken per standard 06.02.10. Collect and report process data in the daily Heat Summary Report. Apply both standard and nonconformance testing.
* Responsible to adjust schedules to maintain productivity at the melt shop, bottom pour, caster, and rolling mill. Determine the lowest cost heat divert solution for off chemistry or manufacturing problem heats while maintaining the Metallus brand. Understand the cost of chemical elements added to steel and the differences between grades of steel. Communicate schedule changes to all affected departments.
* Participate in both internal and external customer audits.
* Learn and maintain proficiency on computer systems at FSP melt shop location as well as bottom pour and strand casting processes.
* Train new Turn Metallurgists.
* Work on a rotating shift basis.
Minimum Qualifications
* High school diploma or equivalent with at least 7 years of experience in steel manufacturing.
Preferred Qualifications
* Associate degree in engineering, technology, mathematics, science, business, supply chain management, or related with at least 4 years of experience in steel manufacturing.
* Bachelor degree in engineering, technology, mathematics, science, business, supply chain management, or related with at least 2 years of experience in steel manufacturing.
The company prohibits harassment or discrimination against any employee on the basis of any status protected by law, including, but not limited to, race, religion, color, national origin, ancestry, age, disability, genetic information, gender, sex or veteran status.
Controls Assurance Auditor
Quality assurance specialist job in Auburn Hills, MI
The Controls Assurance Auditor will support in the scoping, planning, creation and execution of testing of internal controls over financial reporting (“ICFR”) based on the assessment approach to assess the design and operating effectiveness. In addition, this role will involve coordination of test schedule and procedures with the control owners and internal as well as external auditors, as needed. The Controls Assurance Auditor will conduct walkthrough meetings with control owners, execute the entire testing cycle through fieldwork and reporting of the assigned audit areas. The Auditor will perform the assigned test plan consistently with the guidance received and based on the feedback received by the manager during the engagement. The Auditor will also communicate the status and results of ICFR testing procedures to the control owners and will support the team in the communication to other various stakeholders including management and external auditors.
Additional responsibilities include:
Assist with overall scoping and planning procedures for the assessment cycle
Effectively contribute to process improvement initiatives across the organization
Support the development of the audit plan and testing approach
Execute test plans, procedures and processes of business areas' test programs against the testing standards
Create accurate, logical and detailed work papers clearly describing the work performed, results of testing and conclusions reached
Validate accuracy and alignment of relevant ICFR documentation (i.e.: control descriptions, risk/control matrices, mapping of controls to financial statement assertions, etc.)
Create, maintain and revise internal control documentation
Maintain a project plan, which ensures timely completion of ICFR testing in compliance with internal/external audit requirements and deadlines
Provide ongoing testing status updates to team
Support the management of Governance, Risk and Compliance (“GRC“) system maintenance and usage
Coordinate test schedule and procedures with the external auditors and management
Identify and escalate risk exposures to appropriate levels of management
Prepare deficiency language for issues identified during testing procedures and effectively communicate to control owners
Work with the manager in formal written reports to management summarizing audit results
Execute special projects, as assigned
What You'll Learn:
Understand business processes from the initiation of activity through recording, the related controls and risks
Identify potential gaps in risks and controls within the control framework presenting potential exposure to management
Conduct with different levels of management including interviews to perform testing, learn business processes, provide status updates and deliver issues
Perform testing over multiple business processes
Writing skills to document processes and testing procedures
Document deficiency language and appropriately communicating the issues to control owners
Active participation to the team assigned to the audit
Present testing status and communicate issues noted
Assist in preparing reports and presentations to top management
Build relationships with the control owners
Work with other testing teams from different countries to ensure consistency in testing and process documentation
What This Role Will Prepare You For:
Roles (including manager roles) within Group Controls Assurance, Internal Controls and Financial Reporting, Corporate Finance and Corporate Accounting
Haitian Creole Bilingual Quality Assurance Administrator
Quality assurance specialist job in Detroit, MI
Description & Requirements Maximus is currently hiring a remote Haitian Creole Bilingual Quality Assurance Administratorto support the Florida Healthy Kids (FL HK) program operations and ensure compliance with established standards and Florida healthcare policies.
In this role, you will be responsible for monitoring phone calls and completing back-office quality reviews to determine whether employees are meeting required performance, quality, and compliance standards. You will also participate in special projects and program initiatives as needed and serve as backup support for the call center during periods of high volume or operational need.
The ideal candidate demonstrates strong attention to detail, excellent critical thinking and analytical skills, and the ability to accurately interpret and apply Florida healthcare policies. This position requires a high level of organization, consistency, and accountability in a remote work environment.
Essential Duties and Responsibilities:
- Provide assistance to program clients with completion of paperwork and obtains employment verification documentation.
- Support case managers to obtain attendance documentation.
- Scan and log all client documentation in an accurate and timely manner.
- Ensure activities and processes are in compliance with both company QA standards and applicable contractual standards.
- Enter, transcribe, record, store, or maintain information in written, electronic and magnetic form relating to services, processes and quality systems.
- Coordinate review activities as assigned by management.
- Perform general office duties such as filing, copying, faxing and mail.
- Perform other duties as may be assigned by management.
Minimum Requirements
- High school diploma or equivalent with 0 - 2 years of experience.
- Florida residency preferred.
- Florida Healthy Kids Program experience preferred.
- Bilingual proficiency in both English and Haitian Creole required.
Home Office Requirements:
- Desktop or Laptop that runs Windows, Mac, or Linux (no Chromebooks or tablets).
- OS for Windows - Current release of Windows 10 or newer.
- OS for Mac - Big Sur (11.0.1+); MacOS (10.14) or newer.
- OS for Linux - Ubuntu (18.04).
- Connectivity to the internet via either Wi-Fi or RJ-45 connection for wired network connection to home router (no mobile hotspots).
- Internet speed of 25mbps or higher required (you can test this by going to *******************
- USB plug and play wired headset with a microphone (no Bluetooth, AirPods or wireless gaming headsets).
- Must currently and permanently reside in the Continental US.
- Must have a camera
EEO Statement
Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics.
Pay Transparency
Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances.
Accommodations
Maximus provides reasonable accommodations to individuals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at **************************.
Minimum Salary
$
17.00
Maximum Salary
$
18.50
Easy ApplyQuality Assurance Specialist Intern - Summer 2026
Quality assurance specialist job in Detroit, MI
Preferred Qualifications * Self-directed approach * Ability to communicate effectively * Proficiency in the Microsoft Office suite, including Excel, PowerPoint and Word Interns at the Rock Family of Companies gain priceless hands-on experience. Here, they learn how it feels to be in the workplace, participate in events and become a valuable member of our team.
Responsibilities
* Learn about our business by attending meetings, huddles and trainings
* Share creative ideas that will help improve our business
* Deliver reports, analyze metrics and summarize information to help drive our team forward
* Assist in creating materials and/or presentations for meetings
* Take notes during meetings and provide recaps
Disclaimer
This is an outline of the primary responsibilities of this position. As with everything in life, things change. The tasks and responsibilities can be changed, added to, removed, amended, deleted and modified at any time by the leadership group.
QA Compliance Specialist
Quality assurance specialist job in Warren, MI
Responsible for the general compliance of Merit's Quality System to regulatory and industry requirements, ensuring improvements are tracked then trended, support external audits with oversight on internal audits, and support various quality functions.
Essential Functions include but are not limited to the following:
Managing non-conformances, deviations, CAPAs, and DMRs
Support validation program
Assist in regular quality system review and updates
Keep track of Scorecard for all departments training of SOPs on a monthly basis
Regular review of current industry compliance trends
Oversee the internal audit program
Support continuous improvement initiatives
Support supplier qualification program
Perform root cause analysis of various non-conformances and out-of-specifications
Other duties as assigned
Skills/Knowledge/Abilities
Must have a High School Diploma or equivalent (Bachelor's Degree preferred)
2 years of compliance or regulatory experience
Excellent critical analysis skills
Excellent verbal communication skills
Speak and write English
Basic mathematical skills
Basic computer skills
Physical Demands
Sitting 50%
Walking 60%
Standing 30%
Visual Acuity
Ability to lift and pull minimum of 40lbs.
Bending, pulling, pushing, reaching, above shoulder/below waist
Speaking - Ordinary speech
Hearing - Ordinary conversation
Fingering - Computer keyboard
What you get for your Hard Work:
Pay: Starts at $23-25/hr
Benefits:
Healthcare
Dental
Flexible Time Off Policy
Performance Bonus Opportunities
Year End Bonus Opportunity
Company events
Equality:
Merit Manufacturing is committed to the full inclusion of all qualified individuals. All qualified applicants will receive consideration for employment without regard for race, religion, disability, age, sexual orientation, gender identity, national origin, veteran status, or genetic information.
Quality Coordinator (NE)
Quality assurance specialist job in Trenton, MI
Do you have experience in supply chain management, operational analysis, and business process improvement? As a Quality Coordinator you will serve in a consulting and leadership style role while managing the quality of our processes. Join our expanding team to help drive our organization today!
About the Role & How you will contribute
* Train, mentor and coach current and new quality auditors as well as plan, lead, and a coach a team of Quality Auditor's on a daily basis.
* Serve as an initial point of contact for both internal and external customer requests.
* Ensure sufficient quality audit resources are available and provide ongoing & efficient resource planning & allocation.
* Ensure all quality audits on designated processes, area's or departments in line with customer or company criteria both quantity and content wise are performed.
* Ensure First Article Inspections (FAI) and associated reporting is carried out within the agreed SLA's.
* Initiate quality improvement initiatives or support quality improvement projects.
* Ensure periodical (daily, weekly monthly & quarterly) internal and external quality reports are accurate and distributed to the correct audience.
* Promote best practices on quality of product or process to quality auditors and operational staff.
* Maintenance & creation of Quality Control related documentation (WI's QR's and SOP's).
* Other duties as assigned.
Your Key Qualifications
* Experience in Quality auditing in a transport/warehouse environment.
* Knowledge of operational processes and quality auditing.
* Must have prior experience using computers and MS office.
* Must have Excel experience
* Able to communicate in the languages used in the area.
* Capable of performing internal audits.
About the Role
How you will contribute
* Train, mentor and coach current and new quality auditors as well as plan, lead, and a coach a team of Quality Auditor's on a daily basis.
* Serve as an initial point of contact for both internal and external customer requests.
* Ensure sufficient quality audit resources are available and provide ongoing & efficient resource planning & allocation.
* Ensure all quality audits on designated processes, area's or departments in line with customer or company criteria both quantity and content wise are performed.
* Ensure First Article Inspections (FAI) and associated reporting is carried out within the agreed SLA's.
* Initiate quality improvement initiatives or support quality improvement projects.
* Ensure periodical (daily, weekly monthly & quarterly) internal and external quality reports are accurate and distributed to the correct audience.
* Promote best practices on quality of product or process to quality auditors and operational staff.
* Maintenance & creation of Quality Control related documentation (WI's QR's and SOP's).
* Other duties as assigned.
Your Key Qualifications
* Experience in Quality auditing in a transport/warehouse environment.
* Knowledge of operational processes and quality auditing.
* Knowledge using computers and MS office.
* Able to communicate in the languages used in the area.
* Capable of performing internal audits.
Compensation
DP World offers exciting and challenging roles within a growing international organization. We strive to hire and develop the right people, locally and globally, stimulating personal growth and self-development within an informal atmosphere. We offer a market competitive compensation package.
About DP World
Trade is the lifeblood of the global economy, creating opportunities and improving the quality of life for people around the world. DP World exists to make the world's trade flow better, changing what's possible for the customers and communities we serve globally.
With a dedicated, diverse and professional team of more than 111,000 employees from 159 nationalities, spanning 77 countries on six continents, DP World is pushing trade further and faster towards a seamless supply chain that's fit for the future.
We're rapidly transforming and integrating our businesses -- Ports and Terminals, Marine Services, Logistics and Technology - and uniting our global infrastructure with local expertise to create stronger, more efficient end-to-end supply chain solutions that can change the way the world trades.
What's more, we're reshaping the future by investing in innovation. From intelligent delivery systems to automated warehouse stacking, we're at the cutting edge of disruptive technology, pushing the sector towards better ways to trade, minimizing disruptions from the factory floor to the customer's door.
DP World is on a mission to transcend boundaries and bridge the gap between all nations and cultures - not just in what we do but also in how we behave.
We are dedicated to creating a culture where everyone feels respected, supported, and empowered to reach their full potential. We believe that embracing inclusion and diversity drives innovation and growth and helps us connect people, businesses, and societies. Free minds and different perspectives are changing our world, and together we can change what's possible.
The DP World family comprises of syncreon, Imperial and P&O.
WE MAKE TRADE FLOW
TO CHANGE WHAT'S POSSIBLE FOR EVERYONE.
Nearest Major Market: Detroit
Job Segment: Logistics, Supply Chain, QC, Supply Chain Manager, Supply, Operations, Quality
15.5 - Documentation Specialist
Quality assurance specialist job in Detroit, MI
As a Documentation Specialist, you will ensure that our technical documentation is clear, accurate, and aligned with the highest standards. Working closely with subject matter experts and writers, you'll refine content to make it easily accessible and understandable for our target audience.
What You'll Do:
Refine Technical Content: Review and edit technical documents, ensuring clarity, accuracy, and consistency.
Collaborate with Experts: Work with subject matter experts and writers to improve content and guarantee technical correctness.
Quality Control: Identify and correct grammatical errors, formatting issues, and enhance overall document quality.
Maintain Consistency: Create and maintain document templates and style guides to ensure uniformity across all materials.
Document Management: Organize and maintain a library of technical documents for efficient access and retrieval.
Requirements
What You Bring:
Education: A Bachelor's Degree in Computer Science, Information Systems, Engineering, or a related field. A Master's degree may be preferred based on specific project needs.
Experience: Proven experience in editing and reviewing technical documentation with a keen eye for detail and consistency.
Preferred: Experience working with technical content in highly regulated or specialized industries.
Legal Document Specialist (Detroit, MI)
Quality assurance specialist job in Detroit, MI
Full-Time | Hourly | $21 - $23 per hour, plus overtime
About Us We're Proof, a high growth company in the legal tech industry founded in 2017. Our best-in-class legal services platform is trusted by over 3,000 law firms across the U.S. and serves countless pro se parties. Our core offerings, Service of Process and E-Filing, are designed to make legal services more accessible, efficient, and transparent. We are on track to double our business again this year and are looking for dedicated, detail-oriented professionals to join our team as we continue to scale.
If you are passionate about transforming the legal industry and believe in making legal services more affordable and accessible to all, we invite you to join our mission-driven team.
Position Overview
We are seeking a Legal Document Specialist with a legal or paralegal background to support our team in the creation, editing, and preparation of affidavits of service and nonservice for law firms and pro se parties. This role is essential to ensuring legal compliance and the highest level of accuracy in our service of process and e-filing operations.
The ideal candidate will bring expertise in legal documentation, a keen attention to detail, and a thorough understanding of legal language, ensuring our affidavits are precise, compliant, and delivered on time. This is an excellent opportunity for individuals with legal assistant, paralegal, or law firm experience who thrive in fast-paced environments.
Key Responsibilities
Prepare and Edit Legal Affidavits: Draft, review, and edit service of process affidavits for accuracy, completeness, and legal compliance. Ensure all affidavits meet state and federal guidelines.
Quality Assurance: Conduct meticulous reviews of legal documents to ensure accuracy in spelling, grammar, and content.
Compliance Oversight: Ensure all documents are fully compliant with legal standards, including state-specific filing requirements and procedural guidelines.
E-Filing: Prepare and finalize certain affidavits for electronic filing, ensuring proper formatting and accuracy.
Collaboration: Work closely with legal teams, process servers, and other departments to maintain efficient workflows and meet deadlines.
Adaptability: Stay current with evolving legal procedures and process changes, adapting quickly to new technologies and methods.
Qualifications
Legal/Paralegal Expertise: Prior experience working as a paralegal, legal assistant, or in a similar legal environment.
Document Drafting & Review: Strong background in preparing, editing, and reviewing legal documents such as affidavits, legal briefs, or similar materials.
Compliance Knowledge: Familiarity with state and federal legal guidelines related to service of process and e-filing.
Attention to Detail: Exceptional editing and proofreading skills with a focus on accuracy and legal precision.
Organized & Responsible: Demonstrated ability to manage multiple tasks with a high degree of organization and responsibility.
Professional Demeanor: Consistently professional, courteous, and responsive in all communications.
Critical Thinking: Ability to problem-solve and proactively address issues before escalation.
Education: Bachelor's degree or paralegal certification is preferred but not required.
Compensation & Benefits
Hourly Pay: $21 - $23 per hour, plus overtime based on experience and location.
Bonus Plan: Eligible to participate in the company bonus plan.
Comprehensive Benefits: Medical, dental, vision, disability insurance, and 401(k) available.
Flexible Time Off: Enjoy flexible paid time off and holiday policies.
Workplace Equipment: Necessary equipment provided.
Work Hours: A full 8 hours of actual work time (excluding lunch breaks) is expected each workday.
E-Verify
This company participates in E-Verify, for more information view the Participation and Right to Work Posters.
Auto-ApplyQuality Assurance Associate - Pharmaceutical
Quality assurance specialist job in Brighton, MI
Department: Quality Assurance
Job Title: Quality Assurance Associate
Reports to: Quality Assurance Manager
General Description
The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities:
1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations,
2) QA on the floor during all manufacturing operations.
DUTIES AND RESPONSIBILITIES
Essential Duties and Responsibilities:
1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required,
2. Lead/represent QA on project teams in support of new product and manufacturing activities,
3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials,
4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.),
5. Perform review and approval of executed documents,
6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities,
7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance,
8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations,
9. Other duties as defined by Biovire.
Behavioral Expectations:
1. Strong work ethic and ability to accomplish tasks without supervision,
2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture,
3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment,
4. Excellent interpersonal skills with the ability to communicate effectively,
5. Basic computer skills (proficient in Microsoft Office applications),
6. Excellent communication skills, both written and verbal,
7. Possess honesty and integrity with a commitment to the highest legal and ethical standards,
8. Treats every person with courtesy and respect,
9. Knowledge of CGMP and regulatory principles,
10. Commitment to quality in the manufacturing process,
11. Ability to independently analyze and resolve complex issues,
12. Strong sense of initiative, accountability, and responsibility
WORK EXPERIENCE AND EDUCATION REQUIREMENTS
· BS in scientific discipline
· 3+ years experience in the biotech/pharmaceutical industry
preferred
· Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems
Quality Assurance Associate - Pharmaceutical
Quality assurance specialist job in Brighton, MI
Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities:
1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations,
2) QA on the floor during all manufacturing operations.
DUTIES AND RESPONSIBILITIES
Essential Duties and Responsibilities:
1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required,
2. Lead/represent QA on project teams in support of new product and manufacturing activities,
3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials,
4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.),
5. Perform review and approval of executed documents,
6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities,
7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance,
8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations,
9. Other duties as defined by Biovire.
Behavioral Expectations:
1. Strong work ethic and ability to accomplish tasks without supervision,
2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture,
3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment,
4. Excellent interpersonal skills with the ability to communicate effectively,
5. Basic computer skills (proficient in Microsoft Office applications),
6. Excellent communication skills, both written and verbal,
7. Possess honesty and integrity with a commitment to the highest legal and ethical standards,
8. Treats every person with courtesy and respect,
9. Knowledge of CGMP and regulatory principles,
10. Commitment to quality in the manufacturing process,
11. Ability to independently analyze and resolve complex issues,
12. Strong sense of initiative, accountability, and responsibility
WORK EXPERIENCE AND EDUCATION REQUIREMENTS
* BS in scientific discipline
* 3+ years experience in the biotech/pharmaceutical industry preferred
* Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems
Document Scanning Specialist
Quality assurance specialist job in Bloomfield Hills, MI
Job DescriptionAbout Us
Pinnacle Fertility is a leading fertility care platform dedicated to fulfilling dreams by building families. With a network of clinics across the nation, we deliver innovative technology, compassionate patient care, and comprehensive fertility treatments to ensure a personalized, high-touch experience for families on their journey to parenthood. Learn more at **************************
About the Role
The Document Scanning Specialist plays a key role in supporting our team by ensuring that important records are accurately digitized, organized, and maintained. This position is ideal for individuals who are detail-oriented, highly organized, and thrive in structured, independent work environments. As a Document Scanning Specialist, you will contribute to the smooth operation of our office by transforming physical files into accessible digital records that support efficiency and compliance.
We are seeking a Document Scanning Specialist to join our team at IVF Michigan supporting clinics in the following locations:
Ann Arbor, MI
Bloomfield Hills, MI
Grand Blanc, MI
Toledo, OH
his is a part-time, temporary onsite position working Monday through Friday, 8:00 AM - 5:00 PM. The role is expected to last 4-8 weeks, with the potential for extension based on business needs.
Key Responsibilities
Scan, digitize, and organize physical documents into our electronic records system.
Ensure all scanned files are clear, legible, and properly labeled.
Maintain confidentiality and handle sensitive patient information with care.
Follow structured processes for document handling and data integrity.
Identify and flag any issues related to document quality or completeness.
Perform light clerical tasks, such as filing or organizing records.
Other administrative duties as assigned.
Position Requirements
Education & Experience:
High school diploma or equivalent required.
Previous experience in document scanning, data entry, or clerical work preferred but not required.
Skills:
Strong attention to detail and ability to work independently.
Basic computer skills, including experience with scanning software or electronic file management.
Ability to follow structured processes with accuracy.
Strong organizational skills and time management.
Compensation & Benefits
Hourly Rate: $19.00 per hour.
Temporary Position: Guaranteed for 4 weeks, with potential extension based on need.
Diversity & Inclusivity at Pinnacle Fertility
At Pinnacle Fertility, we celebrate and value diversity. We serve everyone, regardless of gender, sexual orientation, race, ethnicity, or religion. Just as we embrace the diversity of our patients, we foster an inclusive work environment where team members feel supported and empowered. We are proud to be an equal-opportunity employer and encourage applicants from all backgrounds, abilities, and life experiences to apply.
15.5 - Documentation Specialist
Quality assurance specialist job in Detroit, MI
As a Documentation Specialist, you will ensure that our technical documentation is clear, accurate, and aligned with the highest standards. Working closely with subject matter experts and writers, you'll refine content to make it easily accessible and understandable for our target audience.
What You'll Do: Refine Technical Content: Review and edit technical documents, ensuring clarity, accuracy, and consistency.
Collaborate with Experts: Work with subject matter experts and writers to improve content and guarantee technical correctness.
Quality Control: Identify and correct grammatical errors, formatting issues, and enhance overall document quality.
Maintain Consistency: Create and maintain document templates and style guides to ensure uniformity across all materials.
Document Management: Organize and maintain a library of technical documents for efficient access and retrieval.
Requirements What You Bring: Education: A Bachelor's Degree in Computer Science, Information Systems, Engineering, or a related field.
A Master's degree may be preferred based on specific project needs.
Experience: Proven experience in editing and reviewing technical documentation with a keen eye for detail and consistency.
Preferred: Experience working with technical content in highly regulated or specialized industries.
Pharmaceutical Quality Assurance Associate
Quality assurance specialist job in Brighton, MI
Job Description
Department: Quality Assurance
Job Title: Quality Assurance Associate
Reports to: Quality Assurance Manager
General Description
The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities:
1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations,
2) QA on the floor during all manufacturing operations.
DUTIES AND RESPONSIBILITIES
Essential Duties and Responsibilities:
1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required,
2. Lead/represent QA on project teams in support of new product and manufacturing activities,
3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials,
4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.),
5. Perform review and approval of executed documents,
6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities,
7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance,
8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations,
9. Other duties as defined by Biovire.
Behavioral Expectations:
1. Strong work ethic and ability to accomplish tasks without supervision,
2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture,
3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment,
4. Excellent interpersonal skills with the ability to communicate effectively,
5. Basic computer skills (proficient in Microsoft Office applications),
6. Excellent communication skills, both written and verbal,
7. Possess honesty and integrity with a commitment to the highest legal and ethical standards,
8. Treats every person with courtesy and respect,
9. Knowledge of CGMP and regulatory principles,
10. Commitment to quality in the manufacturing process,
11. Ability to independently analyze and resolve complex issues,
12. Strong sense of initiative, accountability, and responsibility
WORK EXPERIENCE AND EDUCATION REQUIREMENTS
· BS in scientific discipline
· 3+ years experience in the biotech/pharmaceutical industry
preferred
· Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems