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Join to apply for the Quality Control Manager role at Youngstown Glove Co., LLC
ABOUT YOUNGSTOWN GLOVE CO.:
Youngstown Glove Co. is the leading manufacturer of technical gloves for the Electric Utility market in the United States. We are unwavering in our commitment to making the very best gloves - unmatched in their quality, safety and performance. We are also unwavering in our commitment to identifying, hiring and retaining talented individuals to assist in continuing our market leading position along with shaping the future of our company. As a result of these commitments, we are growing at a very rapid pace and have begun the process of building a state-of-the-art rubber glove factory in Springfield, Missouri. This will complete our mission of offering a total hand protection solution to the Electric Utility worker.
ABOUT YOUNGSTOWN GLOVE CO.:
Youngstown Glove Co. is the leading manufacturer of technical gloves for the Electric Utility market in the United States. We are unwavering in our commitment to making the very best gloves - unmatched in their quality, safety and performance. We are also unwavering in our commitment to identifying, hiring and retaining talented individuals to assist in continuing our market leading position along with shaping the future of our company. As a result of these commitments, we are growing at a very rapid pace and have begun the process of building a state-of-the-art rubber glove factory in Springfield, Missouri. This will complete our mission of offering a total hand protection solution to the Electric Utility worker.
JOB SUMMARY:
We are seeking a highly motivated Quality Control Manager that will oversee the development, implementation, and maintenance of the Quality Management System (QMS) for our rubber glove manufacturing plant. This role entails the creation of the overall QMS and ensures continual compliance with ISO 9001 standards, manages raw materials batch testing, monitors and performs laboratory testing, monitors manufacturing processes, and assists the team in delivering consistent, high-quality products. The ideal candidate will have strong leadership skills, technical expertise in quality control, and extensive experience in a manufacturing environment, specifically under ISO-9001.
KEY RESPONSIBILITIES:
- Quality Management System (QMS):
- Develop, implement, secure, and maintain an ISO 9001-compliant QMS to ensure consistent product quality and regulatory compliance.
- Conduct regular internal audits and coordinate external ISO 9001 audits to maintain certification.
- Update and manage quality documentation, including procedures, work instructions, and records.
- Laboratory Oversight:
- Supervise laboratory operations, ensuring accurate testing of raw materials, in-process samples, and finished liquid latex formulations.
- Validate and maintain laboratory equipment, ensuring calibration and compliance with industry standards.
- Analyze test data to identify trends, address non-conformities, and implement corrective actions.
- Manufacturing Process Monitoring:
- Monitor and evaluate manufacturing processes to ensure adherence to quality standards and specifications.
- Implement statistical process control (SPC) and other quality tools to identify and mitigate process variability.
- Collaborate with production teams to resolve quality issues and optimize process efficiency.
- Non-Conformance and Corrective Actions:
- Investigate product or process non-conformances, determine root causes, and implement corrective and preventive actions (CAPA).
- Continuous Improvement:
- Drive continuous improvement initiatives using methodologies such as Six Sigma.
- Identify opportunities to enhance product quality, reduce waste, and improve operational efficiency.
- Regulatory Compliance:
- Ensure compliance with relevant industry regulations, standards, and customer requirements.
- Stay updated on changes to ISO 9001 standards and other applicable regulations, adapting the QMS as needed.
- Reporting and Communication:
- Prepare and present quality performance reports to senior management, highlighting key metrics and improvement plans.
- Collaborate with cross-functional teams, including production and supply chain, to align quality objectives.
- Foster a culture of quality awareness and continuous improvement across the organization.
QUALIFICATIONS:- Education:
- Bachelor’s degree in Industrial Engineering, Chemistry, Quality Control, Industrial Technology, or a related field (or equivalent combination of education and experience). Advanced degree or certifications (e.g., ASQ CQE, Six Sigma, Lean) preferred.
- Experience:
- Minimum of 3-7 years of experience in quality control, with at least 2 years in a leadership role within a manufacturing environment.
- Proven experience managing an ISO 9001-compliant QMS.
- Experience in laboratory operations and testing, preferably with liquid formulations or chemical manufacturing.
- Skills and Competencies:
- Proficiency in using tools like Microsoft Excel, SPC software, or similar platforms.
- Extensive knowledge of ISO 9001 standards and audit processes.
- Proficiency in quality tools such as SPC, FMEA, root cause analysis, and CAPA.
- Familiarity with laboratory testing methods, equipment calibration, and data analysis.
- Strong problem-solving skills and attention to detail, with the ability to troubleshoot process and quality issues effectively.
- Excellent communication and teamwork skills to collaborate across cross-functional teams.
- Ability to manage multiple priorities and thrive in a fast-paced, dynamic environment.
- Ability to adapt to change positively and effectively.
- Ability to work under general supervision.
- Experience in liquid latex or polymer manufacturing highly preferred.
- Core Values
- Integrity
- Dedication to Quality
- Unwavering commitment to excellence
- Positive Attitude
- Innovative Nature
Physical Requirements
- Ability to stand for extended periods, lift up to 30 lbs., and handle equipment or materials as needed.
- Comfort working in controlled environments (e.g., clean rooms, laboratories, or production floors) with exposure to chemicals, machinery, or noise, following safety protocols.
Work Environment- Full-time position, typically Monday through Friday.
- This position will start in Aurora, MO 65605, then transition in the fall permanently to Springfield, MO 65803.
- Work performed in a combination of laboratory, production, and office settings, with adherence to safety and personal protective equipment (PPE) requirements.
- Collaborative, innovative culture with opportunities for professional development and career growth.
- May require occasional travel for supplier audits or training.
Seniority level
Seniority level
Mid-Senior level
Employment type
Job function
Job function
Quality AssuranceIndustries
Manufacturing
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