190 Quality Control jobs in Ohio

Quality Control Manager

Department: Quality Assurance/Quality Control

Employment Type: Full Time

Location: Ashtabula, OH

Description

ASC Engineered Solutions is seeking a dedicated and experienced Quality Control Manager to lead and oversee our facility's Quality Department. This critical leadership role is responsible for developing, implementing, and maintaining an effective Quality Management System (QMS) in alignment with ISO 9001 standards, customer specifications, and overall company objectives. The ideal candidate will ensure that all products and processes consistently meet internal quality standards, comply with customer requirements, and foster a culture of continuous improvement across the organization.

Key Responsibilities

* Lead and manage the QC department, including the team of inspectors and quality tech.
* Responsible for developing, implementing, and monitoring the facility's quality control system to maintain compliance with ISO 9001 standards.
* Analyze test results and work with production to identify and correct deviations from quality standards.
* Manage non-conformance reports (NCRs), root cause analysis, and corrective/preventive actions (CAPA).
* Oversee inspection requirements for all purchased product.
* Develop and monitor control plans, FMEAs, and standard operating procedures (SOPs).
* Train and coach employees on quality policies, procedures, and inspection techniques.
* Conduct internal quality audits.
* Lead efforts to reduce scrap, rework, and customer complaints through continuous improvement initiatives.
* Maintain overall calibration system.
* Implement Lean manufacturing and quality principles to enhance process efficiency, reduce variation, and ensure product compliance.
* Drive continuous improvement efforts within the quality department using Lean tools and methodologies.
* Support root cause analysis and corrective actions through Lean problem-solving techniques (e.g., 5 Whys, fishbone diagrams, Kaizen events).
* Collaborate closely with Human Resources to coordinate training programs, manage employee performance, and conduct annual evaluations for quality staff.

Skills, Knowledge & Expertise

* Bachelor's degree in Engineering, Quality Management, or a related scientific field, or an equivalent combination of education and experience.
* Minimum of 5 years of experience in a quality-focused role within a manufacturing setting.
* Strong understanding of rubber processing techniques is a plus but not required (e.g., mixing, extrusion, compression/injection molding).
* Knowledge of various inspection methodologies and blueprint interpretation.
* Experience with statistical process control (SPC) and quality tools (e.g., 8D, 5-Why, Pareto Analysis, Six Sigma Tools, DOE).
* Experience in the development, implementation, and maintenance of a robust Quality Management System (QMS) aligned with ISO 9001 standards, ensuring ongoing compliance, continuous improvement, and audit readiness.
* Advanced proficiency in data-driven decision-making to support quality assurance and process optimization.
* Experience with analyzing complex datasets to drive process improvements and ensure regulatory compliance.
* Proficient in MS Office; knowledge of quality management systems (QMS) software is a plus.
* Excellent communication, leadership, and problem-solving skills.

Job Benefits

* Health & Dental
* Life Insurance
* 401(k) with 100% match up to 4%
* STD & LTD
* Variety of Additional Supplemental Insurances
* Company Paid Holidays, Vacation & PTO

If you are a QC Manager with large scale ground-up commercial and/or light industrial project experience please apply!

Top Reasons to Work with Us

Highly Reputable

What You Will Be Doing

Essential Duties and Responsibilities:

Lead planning, development, and implementation of the Quality Management Plan and system for all work divisions from notice to proceed through final customer acceptance.
Maintain, monitor and update the USACE RMS system. Finalize and load pay requests into RMS.
Establish and lead quality control initiatives, activities, and corrective actions.
Review project specifications for project quality requirements.
Review shop drawings and submittals for conformance with project specifications by direct review and by leveraging the knowledge and experience of others in the project team when necessary.
Host and document weekly QC meetings with the superintendent and provide written minutes as described in project contract documents.
Manage Non-Conformance Notices and the Request for Information process though corrective action.
Manage and resolve issues in conjunction with the project superintendent.
Quality control daily reports that reinforce activities that are being constructed in conformance with each specific project's established standard and constructively confronts non-conformances to produce the desired outcome in a timely manner.
Create, update and maintain the project submittal log and all other project specific quality control reports.
Conduct preparatory, initial and follow up meetings to establish an understanding of the standards of care desired for each definable feature of work. Verify that checklists are being used and signed off prior to the placement of concrete, steel and other similar items of work.
Verify and document that all materials received for the project are in conformance with the approved submittal, are handled and stored appropriately and are acceptable for use in the project.
Conduct preconstruction meetings with new and existing subcontractors and the superintendent at least two days prior to the start of each new phase of the work to discuss issues that affect quality. Document these meetings in the daily QC report and Preparatory Phase reports.
Schedule, document the results of, and maintain a log of all code and independent inspections that are required. Clearly document, correct and re-inspect all non-conformances prior to covering up work.
Conduct periodic follow up inspections to verify that work is proceeding with the contract documents and the approved submittals. (Desired results come from what is inspected, not what is expected.)
Coordinate and document the testing and commissioning of building systems.
Document and distribute pre-punch lists, punch lists and the completion of these lists.
Document final inspections, certificates of occupancy and acceptance of the works and various phases thereof.
Maintain the project "as-built" drawings on a daily basis.
Assemble and forward project closeout documents that include O
M manuals, as-builts and warranties.
Stop work if necessary to resolve matters that affect safety, quality and/or inhibit the logical progress of work.

What You Need for this Position

Education: Bachelors Degree in Civil Engineering, Construction Management, or related field preferred. ICC certification as a Commercial Building Inspector will be considered.

Experience: Possess at least seven (5) years of relevant construction experience with at least three (3) years of construction quality control experience. USACE QCS/RMS experience is preferred.

Knowledge, Skill, and Abilities:

American Society for Quality (ASQ), International Organization for Standards (ISO), or other quality management training and certification desired.
OSHA 30 hourStrong organizational, interpersonal skills.
CQM Certification.
Technical knowledge of materials and construction concepts.
Enforce all regulatory, base and company specific safety rules.
Demonstrated ability to work accurately, follow procedures and schedules, and prioritize multiple tasks.
Proficiency with all MS Office products (Word, Excel, Access, PowerPoint).
Ability to work in a team environment and fit in with company culture and processes.

What's In It for You

Great Salary and Benefits, Including lucrative bonus structure
Great long term potential!

So, if you are a QC Manager with large scale commercial project experience, please apply today!

Job Description:

Ryan Companies US, Inc. has an immediate career opportunity for a Quality Control Manager to join our national Mission Critical sector team in Atlanta!

Do you bring at last 5 years of successful field quality management experience in mission critical construction? Do you enjoy working in a fast, fun, inclusive and collaborative work space? Do you want the next chapter of your career to be with an industry leader in commercial real estate who brings a fully integrated and creative design-build approach? If this describes you, we encourage you to apply today.

Some things you can expect to do:

* Lead the planning, development, and implementation of Ryan's quality program for data centers.


* Responsible for managing and performing the daily QC responsibilities of specific projects to ensure the project is constructed in accordance with the established contract documents.


* Lead and train other project team members on quality-related activities.


* The Quality manager role includes direct oversight and review of the entire documentation and physical inspection phase of the workflow process and working with other in-house personnel (e.g.: Project Managers, Superintendents, etc.) and external personnel to produce and document a quality product.


* Review shop drawings and submittals for conformance with project specifications by direct review, and by leveraging the knowledge and experience of others in the project team when necessary.


* Participate in preparatory meetings to establish an understanding of the standards of care desired for each scope of work.


* Participate in pre-installation meetings with new and existing subcontractors, project team members, and any other stakeholders, prior to the start of each new phase of the work, to discuss issues that affect quality.


* Ensure project team members, trade partners, and all stakeholders understand the quality management requirements, for each scope of work.


* Set quality management expectations, including the quantity and timing of field inspections, testing requirements, and documentation requirements for each scope of work.


* Verify and document that all materials received for the project are in conformance with the approved submittal, are handled and stored appropriately, and are installed and acceptable for use in the project.


* Conduct, participate in, or assign quality management tasks to other project team members.


* Monitor, Track, Log and Audit all quality control activities, including all testing, inspections, and supporting documentation throughout the project.


* Monitor, Track, and support the project team to verify effective implementation of corrective actions for project non-conformances and quality issues.


* Conduct Root Cause Analysis to identify, resolve and implement solutions to quality issues


* Conduct and document weekly QC meetings with the superintendent, and provide and distribute written minutes, as described in project specific contract document.


* Conduct periodic quality walkthroughs with the client, the design team, and/or any other client quality representative.


* Conduct and document weekly QC Meetings with the client and provide and distribute meeting minutes.


* Provide weekly QC reports that reinforce activities that are being constructed in conformance with each specific project's established standard and constructively confronts any non-conformance to produce the desired outcome in a timely manner.


* Support the project team with punch list and other phase turnover activities.


* Stop work if necessary to resolve matters that affect safety, quality and/or inhibit the logical progress of work.


* Capture and share lessons learned with the project team, trade partners, and other Ryan Mission Critical project teams.



Job Requirements:

* To be successful in this role, a technical degree in construction, civil, architecture, engineering, or equivalent is required. You must have at least 5 years of experiences in design, construction, and/or commissioning for large & complex MEP-heavy projects. Previous experience leading construction documentation and contract administration is required.



You will really stand out if you have:

* Knowledge of one or more quality systems (i.e., Malcolm Baldridge, ISO 9000, Lean, Kaizen, Army Corps of Engineers, etc.


* Experience using Procore, Bluebeam, and Revit



Eligibility:

* Positions require verification of employment eligibility to work in the U.S.


* Must be authorized to work in the U.S.



Benefits:

* Competitive Salary


* Medical, Dental and Vision Benefits


* Retirement and Savings Benefits


* Flexible Spending Accounts


* Life Insurance


* Educational Assistance


* Paid Time Off (PTO)


* Parenting Benefits


* Long-term Disability


* Ryan Foundation - charitable matching funds


* Paid Time for Volunteer Events



Ryan Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Non-Solicitation Notice to Recruitment Agencies:

Ryan Companies kindly requests that recruitment agencies and third-party recruiters do not submit unsolicited resumes or candidate information to any Ryan Companies employee or office. Ryan Companies will not be responsible for any fees or expenses associated with unsolicited submissions. If recruitment services are required, we will reach out directly to agencies on our approved vendor list. We appreciate your understanding and cooperation.

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!

Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.

Why you'll love working at Axogen:

* Friendly, open, and fun team culture that values unique perspectives
* Company-wide dedication to profoundly impacting patients' lives
* Comprehensive, high-quality benefits package effective on date of hire
* Educational assistance available for all employees
* Matching 401(k) retirement plan
* Paid holidays, including floating holidays, to be used at your discretion
* Employee Stock Purchase Plan
* Referral incentive program

Axogen Mission and Business Purpose

Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.

Job Summary of the Director, Quality Control

The Quality Control Director is responsible for the oversight of all Quality Control Laboratory functions, activities, and personnel at the Axogen Processing Center (APC) and associated contract laboratories. This includes all analyses done on donor tissue, raw materials, and in process, product release, environmental monitoring, and commercial product stability samples. Additionally, the Quality Control Director builds and maintains collaborative work relationships with APC and company Operations, Quality Assurance, Finance, and Regulatory leaders to drive cross-functional planning and decision-making regarding Quality Control Laboratory operations and process improvement.

Requirements of the Director, Quality Control

* Bachelor's degree in chemistry, biology or other sciences related field.
* Minimum of ten (10) years of relevant industry experience.
* Minimum of six (6) years QC supervisory experience (hiring and coaching associates and supervisors).
* Strong laboratory skills (microbiology, histology, and incoming quality control).
* Experience in the validation and transfer of analytical methods from/to R&D and/or contract laboratories.
* Experience working in sterile processing environment.
* Experience working in an FDA or AATB regulated industry.
* Strong skills in communicating technical and scientific information.
* Strong organizational and problem-solving skills.

Responsibilities of the Director, Quality Control

The specific duties of the Director, Quality Control include but are not limited to:

* Leads the APC Quality Control Laboratory, including organizational design, operating budget, personnel recruiting, and employee technical and behavioral competency development and training.
* Collaborates across the company representing the Quality Control Laboratory, engaging with stakeholders and business partners in both a technical and management leadership capacity.
* Ensures the Quality Control support strategy for the APC site is technically sound and in alignment with business objectives and quality/regulatory requirements. Owns key laboratory QMS processes, including deviations, CAPA actions, implementing compendia changes, technical problem solving, and monitoring operational results via trend analyses.
* Creates an environment with strong team spirit, timely and effective communication, sense of urgency and high motivation, and inspires Quality Control team members to achieve short and long-term goals.
* Sets an expectation of achieving outcomes, continuous learning, and shared accountability; champions a mindset of inclusivity, speaking up, and coaching others.
* Takes proactive measures to promote a positive safety culture and ensure all applicable safety, health and environmental requirements are met in accordance with company policies.
* Embodies Lean principles and methodologies and promotes a continuous improvement culture throughout the Quality Control organization by encouraging experimentation and learning.
* Provides laboratory oversite regarding Out of Specification results and associated investigations, both with internal and external contract testing laboratories.
* Represents the Quality Control Lab during regulatory inspections and internal audits.
* Performs all other duties as assigned.

Location

913 Industrial Drive Place, Vandalia, OH 45377

#LI-AC1

Benefits/Compensation

This position is eligible for an annual bonus.

Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.

Salary Range

$163,910-$204,887 USD

Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion.

Job Description

Job Title: Quality Control Manager - Welding Industry
Location: Cleveland, OH
Full-Time | Flexible 1st Shift Hours
Salary: $80,000 - $0,000 (Based on Experience)
Full Benefits Package Included

About Us:

We are a leading steel fabrication company based in Cleveland, Ohio, with a strong reputation in the bridge construction and welding industry. Our team is committed to excellence in fabrication quality, safety, and compliance, and we are looking for an experienced Quality Control Manager to ensure our operations meet the highest industry standards.

Position Overview:

As a Quality Control Manager, you will oversee all aspects of welding quality control and compliance. You will ensure that welds and fabrication processes meet or exceed industry codes, maintain QA documentation, and lead internal and external audit processes. This is a hands-on leadership role ideal for someone with deep experience in welding and inspection, and a strong working knowledge of industry standards such as AWS, AISC, ISO, and NDT protocols.

Key Responsibilities:

• Oversee and implement all quality control procedures for welding and fabrication processes.
• Ensure compliance with AISC Bridge Code, ISO 9001, and other applicable standards.
• Maintain and organize QA/QC documentation for inspections, audits, and certifications.
• Schedule and track internal audits and third-party inspections.
• Work closely with production and engineering to resolve welding and quality issues.
• Review and approve Welding Procedure Specifications (WPS) and Procedure Qualification Records (PQR).
• Supervise Non-Destructive Testing (NDT) processes and evaluate results.
• Lead root cause analysis and implement corrective actions.
• Train and mentor welders and quality team members on best practices and code compliance.
• Act as primary contact for quality matters during client audits and regulatory inspections.

Requirements:

• 5+ years of experience in Welding Quality Control, preferably in structural steel or bridge fabrication.
• Must have a strong understanding of welding processes (SMAW, FCAW, GMAW, GTAW) and fabrication standards.
• Certification or familiarity with:
  • Certified Welding Inspector (CWI)
  • Non-Destructive Testing (NDT) methods
  • AISC Bridge Code
  • ISO 9001 Quality Systems
• Strong communication and documentation skills.
• Familiarity with QA software or digital inspection tools is a plus.
• Excellent organizational and problem-solving abilities.

What We Offer:

• Competitive Salary: 80,000- 90,000 based on experience.
• Flexible 1st Shift Schedule (M-F).
• Comprehensive Benefits Package:
  • Medical, Dental, Vision
  • 401(k) with Company Match
  • Paid Vacation & Holidays
  • Ongoing Training and Certification Reimbursement
• A supportive, team-oriented environment focused on safety, quality, and growth.

Keywords:

Welding Quality Control, CWI, AWS D1.1, AISC Certified Fabricator, Welding Inspector, ISO 9001, NDT Level II, Bridge Welding Code, Structural Steel, Weld Audit, WPS, PQR, SMAW, FCAW, GMAW, Welding Supervisor, QA/QC, Fabrication Quality, Welding Certification, Quality Assurance Manager, Cleveland Welding Jobs, Manufacturing QA, Steel Fabrication, Welding Code Compliance, Welding Process Control.

If you feel you have the above qualifications, please apply for immediate consideration.

All qualified applicants will receive consideration for employment without regard to race, color, religion, ethnicity, national origin, sex, gender identity, sexual orientation, disability status, protected veteran status or any other protected status under the law.

EverStaff is an equal opportunity employer (M/F/D/V/SO/GI)

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit About the Role: We are seeking an experienced Quality Control Manager to join our Quality Unit at our large-scale, non-sterile compounding pharmacy located in New Albany, OH. The Quality Control Manager will play a critical leadership role in driving continuous improvement initiatives that ensure the highest quality products for our patients and customers. Reporting to the Director of Quality, this role will oversee quality control operations, lead in-process and final product inspections, and ensure compliance with USP standards, cGMP practices, internal SOPs, and applicable regulatory requirements. You Will: * Lead and perform in-process and post-production quality checks, including product inspection, testing, and disposition at various stages of the compounding process. * Manage day-to-day activities on the production floor to ensure product and raw material compliance. * Compile, analyze, and present trending data and quality reports to QA management. * Oversee investigations related to non-conformances, deviations, and customer complaints, and drive root cause analysis and corrective actions. * Manage the product retain program and ensure timely and compliant inspections. * Collaborate with production and pharmacy teams to implement quality improvement initiatives. * Maintain oversight of critical equipment verifications (e.g., pH meters, balances) and calibrations. * Review and approve compound records, Certificates of Analysis (COAs), and raw material documentation to ensure quality standards are met. * Draft, revise, and implement SOPs, protocols, and related documentation in alignment with USP standards and regulatory requirements. * Ensure ongoing compliance with USP <795> guidelines for non-sterile compounding and applicable cGMP practices. * Support internal audits and external third-party inspections. * Manage relationships with contract laboratories for external product testing. * Train and mentor pharmacy and production staff on quality standards, processes, and procedures. * Have a Pharmacy Technician license or be willing to obtain one within your first six months of employment (we cover costs and will help you obtain your trainee hours). You Have: * Bachelor's degree in Chemistry, Biology, Pharmacy, Quality Management, Engineering, or related discipline (preferred). * 3+ years of experience in quality control or quality assurance, ideally in a non-sterile compounding or pharmaceutical manufacturing environment. * Strong working knowledge of USP <795> and applicable cGMP standards. * Experience in a regulated environment (FDA 21 CFR 210/211 experience a plus). * Proven leadership skills with the ability to coach and develop quality and production personnel. * Exceptional interpersonal, verbal, and written communication skills. * Strong proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook); MRP system experience preferred. * Ability to manage multiple priorities, work independently, and maintain high attention to detail. * Strong technical writing skills for SOPs, protocols, and reports. * Familiarity with quality metrics, root cause analysis, and statistical quality control methods. * Proven ability to build and maintain strong cross-functional partnerships, paired with clear, effective communication across all levels of the organization. Nice to Have: * Experience working in a 503A or 503B compounding facility. * Prior management of environmental monitoring or contamination control programs. * Experience supporting facility expansions, FDA inspections, or operational scale-up projects. Our Benefits (there are more but here are some highlights): * Competitive salary & equity compensation for full-time roles * Unlimited PTO, company holidays, and quarterly mental health days * Comprehensive health benefits including medical, dental & vision, and parental leave * Employee Stock Purchase Program (ESPP) * 401k benefits with employer matching contribution * Offsite team retreats Conditions of Employment: * This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required. * This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR). * Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs. * Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs. We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match. Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address. To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

On-Board Services is hiring a Quality Control Manager in
Cleveland, OH   
For immediate consideration please send your resume to
Subject Line: Position Title and State you are located

 
About Us:
On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.
 
Position Details:
Title: Quality Control Manager
Position Type: 1 year contract with additional opportunity contingent upon performance and continued business need
Job Location : Cleveland, OH  
Shift: 1^st Shift 7AM-3:30PM
Benefits : 401K, Dental insurance, Life Insurance, Medical Insurance, Vision Insurance 
Compensation: $48/HR
 
Position Summary
The Quality Control Manager oversees daily operations of the quality control laboratory, ensuring accurate and timely testing, maintaining instrument performance, and leading a team of laboratory staff. This role drives continuous improvement through data-driven analysis of key performance indicators (KPIs) while ensuring compliance with internal and external quality standards.

Key Responsibilities

• Supervise laboratory personnel, including hiring, training, scheduling, and performance evaluations.
• Foster a culture of accountability, safety, and continuous improvement.
• Ensure testing results are delivered on time to meet production and customer requirements.
• Monitor workflow and allocate resources to maintain efficiency and accuracy.
• Oversee maintenance, calibration, and qualification of laboratory instruments.
• Troubleshoot equipment issues and coordinate vendor repairs and upgrades.
• Ensure testing procedures comply with quality standards (e.g., ISO 9001, IATF 16949).
• Conduct internal audits and support external inspections.
• Track and analyze laboratory KPIs, including turnaround time, error rates, and equipment uptime.
• Use data to identify trends, root causes, and process improvement opportunities.
• Maintain accurate records of testing, maintenance, and personnel training.
• Prepare reports for senior management and customers.

Qualifications

• Bachelor’s degree in Chemistry, Biology, or related scientific field.
• Minimum 5 years of laboratory experience, including at least 2 years in a supervisory role.
• Demonstrated expertise in instrument maintenance and troubleshooting.
• Strong knowledge of laboratory workflows and quality control practices.
• Proficiency in data analysis tools (Excel, LIMS, SPC software).
• Excellent communication, leadership, and organizational skills.
• Familiarity with quality management standards (ISO 9001, IATF 16949).

Apply Today!

 
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.

The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC.  On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”

On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.
 
JD#
INDOJ
 
 

Description
Summary:
The Quality Control Specialist 1 executes against assigned control tests as part of the overall first line of defense testing program. Control tests may include but will not be limited to oversight and effective challenge of operational processes such as case investigation, transaction monitoring, OFAC Compliance, CTR & MIL, and due diligence reviews. This position acts as individual contributor who can effectively and tactfully provide oversight and effective challenge on reviews of individual work items as well as execute against department strategies that ensure compliance with BSA/AML/CTF regulations in alignment with Huntington's risk appetite.
Duties and Responsibilities:
+ Under direct supervision, the colleague will primarily execute against assigned control tests including each of the core functions of BSA/AML and OFAC Compliance programs.
+ The colleague will partner with QC Leadership to identify opportunities for continuous education, mentorship, and colleague development.
+ The colleague will serve as an internal leader related to BSA/AML and OFAC compliance and provide feedback to QC Leadership.
+ The colleague will develop and maintain strong working relationships with operational colleagues to ensure continuous and proactive communication to QC leadership.
+ The colleague may be assigned special projects from time-to-time and under the direct supervision of QC Leadership, which may include the development of procedures, new control tests or adjustments to existing control tests, and other projects to assist in continuous improvement of the unit's effectiveness.
+ Performs other duties as assigned.
Basic Qualifications:
+ Bachelor's Degree or in lieu of Bachelor's Degree, a high school diploma with an additional 4 years of relevant banking or financial experience.
+ Two or more years of experience in financial/banking industry or BSA/AML department specifically to also include at least one year in an investigation or testing, risk & control, or audit role.
Preferred Qualifications:
+ At least one year of experience with colleague coaching and leadership through indirect or direct management positions.
+ Related professional certifications such as CAMS or CFE
+ Expanded knowledge of federal regulations (USA PATRIOT Act, Bank Secrecy Act, Federal Financial Institutions Examination Council etc.)
+ Strong ability to influence via written communication.
+ Proficient in Microsoft Word, Excel, and Outlook.
+ Excellent critical thinking, communication, interpersonal and organizational skills.
+ Strong analytical and problem-solving skills.
+ Strong attention to detail.
+ Self-motivated, deadline driven and able to work in an ever-changing environment.
+ Familiarity in using AML compliance monitoring systems such as SAS, Actimize Case Management, and other core transaction system (e.g., wire transfer, depository systems, and ACH).
+ Proven track record of strong communications, analytical, organizational, project management and planning skills.
+ Experience with working in team-oriented environments where success of the overall team is critical to operational excellence.
Exempt Status: (Yes = not eligible for overtime pay) (No = eligible for overtime pay)
No
Workplace Type:
Remote
Our Approach to Office Workplace Type
Certain positions outside our branch network may be eligible for a flexible work arrangement. We're combining the best of both worlds: in-office and work from home. Our approach enables our teams to deepen connections, maintain a strong community, and do their best work. Remote roles will also have the opportunity to come together in our offices for moments that matter. Specific work arrangements will be provided by the hiring team.
Huntington will not sponsor applicants for this position for immigration benefits, including but not limited to assisting with obtaining work permission for F-1 students, H-1B professionals, O-1 workers, TN workers, E-3 workers, among other immigration statuses. Applicants must be currently authorized to work in the United States on a full-time basis.
Huntington is an Equal Opportunity Employer.
Tobacco-Free Hiring Practice: Visit Huntington's Career Web Site for more details.
Note to Agency Recruiters: Huntington will not pay a fee for any placement resulting from the receipt of an unsolicited resume. All unsolicited resumes sent to any Huntington colleagues, directly or indirectly, will be considered Huntington property. Recruiting agencies must have a valid, written and fully executed Master Service Agreement and Statement of Work for consideration.

Quality Control Technician
INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: BROWOODRUFF @ ACTALENTSERVICES.COM
Job Description
The Quality Control Chemist performs qualitative and quantitative testing of raw materials, intermediates, and finished products, as well as other samples for quality control, product development, and regulatory conformance. The role involves analyzing raw materials, intermediates, and finished products using, FCC, USP, and AOAC wet chemical and instrumental testing methods. Microbiological testing may also be required.
Responsibilities
+ Analyze raw materials, intermediates, and finished products using various wet chemical and instrumental testing methods.
+ Perform microbiological testing as trained and required.
+ Provide first-line operation and day-to-day instrument and data system maintenance and calibration.
+ Validate test instruments and methods as required.
+ Perform project analysis in support of QA, QC, Divisional, and Regulatory requirements.
+ Assist other departments and lab members with analytical testing and results.
+ Conform to documented Roles and Responsibilities for this position.
+ Maintain timely and complete test method certification.
+ Perform all related quality testing and quality process responsibilities assigned by the Supervisor.
Essential Skills
+ Strong knowledge in chemistry and laboratory techniques.
+ Experience in quality control and assurance processes.
+ Proficiency in wet chemistry, microbiology, and instrumental analysis.
+ Understanding of Quality Systems: GLP, SQF, ISO-9001, HACCP.
+ BS or BA in Chemistry, Food Science, Biology or a related field with Chemistry coursework, or 3-5 years of experience in food quality if no degree.
Additional Skills & Qualifications
+ Familiarity with SAP is preferred.
+ Functional understanding of quality systems can lead to higher compensation.
Pay and Benefits
The pay range for this position is $20.00 - $22.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in ELYRIA,OH.
Application Deadline
This position is anticipated to close on Sep 17, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.