Top 9 Laboratory quality assessment coordinator Jobs in Columbus

ISO/QA Coordinator
Capital Resin Corp —Columbus, OH
- $65,000 - $85,000 a year
- Mid-level
- Analysis skills
- Project management
Clinical Research Coordinator
OhioHealth —Columbus, OH
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Bachelor of Science
Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills
BPC Redaction Clinical Research Assistant
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills
Treatment Plant Operations Manager - 20102459
State of Ohio - Rehabilitation & Correction - Pickaway Correctional Institution —Orient, OH
- $32.35 an hour
- Online Application
- Research
- Driver's License
- Supervising experience
- Paid holidays
- Health insurance
Licensed Practical Nurse (Part-time)
State of Ohio - Developmental Disabilities - Columbus Developmental Center —Columbus, OH
- $27.56 an hour
- Overtime
- Nursing
- Hospital
- HIPAA
- Paid holidays
- Health insurance
10d
Licensed Practical Nurse (Full-time)
State of Ohio - Developmental Disabilities - Columbus Developmental Center —Columbus, OH
- $27.56 an hour
- Overtime
- Nursing
- Hospital
- HIPAA
- Paid holidays
- Health insurance
10d
Psychiatric Advanced Practice Provider - Center for Autism Services and Transition
Ohio State University Physicians —Hilliard, OH
- $105,799.52 - $168,339.16 a year
- Full-time
- Nursing
- Psychiatry
- RN License
- Wellness program
- Paid holidays
7h

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Ohio University (Dublin) Physician Assistant Program —Dublin, OH
While the DCE retains responsibility for academic oversight, curricular alignment, site development strategy, and clinical decision-making, the CEC provides the…
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Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
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ISO/QA Coordinator
Capital Resin Corp —Columbus, OH
Combination of office, laboratory, and manufacturing plant environments. Bachelor’s Degree in in Chemistry, Quality Assurance, Business Administration,…
$65,000 - $85,000 a year
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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ISO/QA Coordinator

Capital Resin Corp
Columbus, OH

Apply Now

Job Details

$65,000 - $85,000 a year

Qualifications

Customer communication
ISO certification audits
Manufacturing facility experience
Bachelor's degree
Laboratory techniques
Chemical plant experience
Factory experience

Full Job Description

Capital Resin Corporation (CRC) is passionate about innovation and pushing the boundaries of customer service. Our focus is helping companies create new and innovative organic chemistries, or improving upon current chemistries, to deliver greater consistency and process stability.

We manufacture and sell engineered chemistries as well as design and build chemical processes for a variety of Fortune 500 companies. We deliver transformational results.

Who we are.

Capital Resin Corporation is a 24/7 production environment dedicated to quality and customer responsiveness. We’ve had significant growth in the past few years and are continuing to build upon that growth. As such, we are always interested in communicating with those individuals who are adaptive, creative, responsive, logical, able to make quick decisions and the best at being a team player. Positions that we seek may include chemical operators, supervisors, chemists, engineers, and salespersons.

About the Role:

This position is responsible for maintaining all quality-related activities as it pertains to CRC’s customers and ISO compliance. This position is based in our Columbus, Ohio Plant. This position will require 5% to 8% travel to our Detroit, Michigan facility and for supplier visits.

Responsibilities:

Quality Management System (QMS) Oversight: Maintain, update and continuously improve the QMS to ensure compliance with ISO:9001 standard, customer requirements and strategic business objectives.
ISO Compliance Management: Coordinate activities related to ISO 9001 certification, surveillance audits, and recertification cycles.
Internal Audits: Plan, schedule, and conduct internal audits, train and maintain an internal auditor team, track findings, verify corrective actions, and prepare audit reports. Conduct calibration and retain audits in QC department to ensure compliance with all SOPs.
Document Control: Manage all controlled documents and ensure proper revision control and accessibility.
Corrective and Preventive Actions: Lead CAPA investigations using structured problem‑solving tools (8D, 5-Whys) including working cross-departmentally to determine root cause, issue reports within the appropriate timeframe, and verify effectiveness of all corrective and preventative actions.
Training Coordination: Maintain training records, support new-hire onboarding, and ensure all relevant associates are trained on appropriate quality tests, including annual refresher training.
Nonconformance Management: Log, investigate, and close nonconformances; collaborate with operations, QC, and R&D to prevent recurrence.
Supplier Quality Support: Assist with supplier evaluations, audits, and performance monitoring.
Data Analysis and Reporting: Analyze data from all quality metrics and key performance indicators (KPIs). Report trends, deficiencies or problems to upper management in management review meetings or report to appropriate personnel.
Continuous Improvement: Identify opportunities to streamline processes, reduce waste, and improve quality performance. Conduct quarterly R&R studies to identify issues and improve the quality test methods. Review all Management of Change (MOC) requests to ensure all quality risks are identified and determine opportunities to lower all quality risks. Observe manufacturing to enhance job knowledge.
Customer Support: Support customer audits, respond to quality questionnaires, complete recertification testing promptly, serve as subject-matter-expert on certificates of analysis (COA) and support sales with all quality-related questions.
Product Support: Attend all pre- and post-production meetings to ensure ISO compliance and to act as a liaison between QC and production.
QC Support: Provide seamless and consistent support to our daily production, serve as a technical expert on test methods and instrumentation. Ability to support any gaps in QC lab coverage.
Quality Culture: Continuously promote quality culture by publishing quality newsletter, engaging with all departments across all shifts and encouraging ISO compliance.
Other: Participate in Process Safety Management (PSM) compliance activities and support the Environmental, Health, Safety and Quality management software.

Qualifications / Requirements / Experience:

Education:

Bachelor’s Degree in in Chemistry, Quality Assurance, Business Administration, Engineering, Industrial Technology or a related field is required.

Experience:

3 to 5 years of chemical laboratory experience is required.
Two to five years of experience in quality assurance, document control, auditing, or quality systems administration preferred.
Experience in a manufacturing environment required.
Chemical manufacturing experience preferred
Experience working with ISO 9001 Quality Management Systems required.

Certifications

This position will be required to obtain the “ISO Lead Auditor Training” certification within the first 6-months on the job.

The following certifications would be a bonus:

ASQ Certified Quality Improvement Associate (CQIA)
ASQ Certified Quality Auditor (CQA)
ISO 9001 Internal Auditor or Lead Auditor Certification
Six Sigma Green Belt or equivalent

Knowledge, Skills, and Abilities

Thorough understanding of ISO 9001 requirements and quality management principles.
Knowledge of auditing techniques and corrective action processes.
Strong document control and record management skills.
Ability to conduct root cause investigations and analyze data.
Excellent organizational and project management abilities.
Strong written and verbal communication skills.
Proficiency in Microsoft Office and quality management software systems.
Ability to work independently and collaboratively with all organizational levels.

Physical Requirements

Ability to work in both office and manufacturing environments.
Ability to stand, walk, and conduct plant audits.
Ability to occasionally lift up to 25 pounds.
Ability to use computers and office equipment for extended periods.

Work Environment

Combination of office, laboratory, and manufacturing plant environments.
Regular interaction with production, laboratory, maintenance, engineering, and management personnel.
Occasional exposure to manufacturing operations, chemicals, noise, and industrial equipment.
Occasional travel for training, audits, customer visits, or supplier assessments.

If you are a motivated individual with a strong attention to detail, we encourage you to apply for this position. We offer competitive pay, benefits, and opportunities for career growth within our organization.

EOE M/F/D/V

Apply Now

Refine Your Search

laboratory quality assessment coordinator jobs in columbus

ISO/QA Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator I - RI Behav Trials Off

BPC Redaction Clinical Research Assistant

Treatment Plant Operations Manager - 20102459

Licensed Practical Nurse (Part-time)

Licensed Practical Nurse (Full-time)

Psychiatric Advanced Practice Provider - Center for Autism Services and Transition

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