Higley Industries Inc
Since 1923, Higley Industries has been at the forefront of the cleaning supply industry, dedicated to producing high-quality products for Industrial, Janitorial, Retail, and Private Label markets. As a company open to the public, we are committed not only to innovation and customer satisfaction but also to environmental stewardship. We strive to minimize our environmental footprint by implementing sustainable practices in our manufacturing processes and product development. Our goal is to lead the industry towards a more sustainable future, ensuring that we meet today’s needs without compromising the ability of future generations to meet theirs.
Job Overview The Quality Assurance Coordinator is responsible for overseeing quality control and quality assurance processes to ensure all manufactured products meet established quality, safety, and regulatory requirements. This role works closely with laboratory and operations teams to support compliance with
FDA regulations ,
cGMP , and
ISO standards , while driving continuous improvement across quality systems. The Coordinator is responsible for SOP implementation, quality documentation, laboratory and testing oversight, and regulatory readiness, ensuring consistent, accurate, and compliant manufacturing operations.
Key Responsibilities
Own, author, review, and maintain
Standard Operating Procedures (SOPs)
and quality documentation
Enforce SOP compliance across production and operations
Support and maintain the
Quality Management System (QMS)
Perform and oversee
basic chemical handling and quality control testing
Lead and support
internal audits
and preparation for
external audits
(FDA, ISO, customer)
Ensure ongoing compliance with
FDA regulations
and
ISO standards
(ISO 9001 or similar)
Coordinate corrective and preventive actions (CAPA) and root‑cause investigations
Train employees on SOPs, quality standards, and compliance requirements
Act as a primary point of contact for quality‑related issues and continuous improvement initiatives
Qualifications
3+ years of experience in
Quality Assurance
within a regulated manufacturing environment
Strong experience with
FDA‑regulated operations
Working knowledge of
ISO standards
(ISO 9001 or similar)
Hands‑on experience with
SOP authoring, enforcement, and documentation control
Experience with
basic chemical handling
and
quality control testing
Ability to work
independently and proactively
in an on‑site manufacturing setting
Strong written and verbal communication skills
Preferred Qualifications
Experience in
chemical manufacturing
or related industries
Experience leading or supporting regulatory and customer audits
CAPA, deviation investigation, and root‑cause analysis experience
Quality certifications (ASQ, ISO Auditor, Lean, Six Sigma)
Why you’ll love working here
Competitive Pay:
Starting salary of $55,000‑$63,000, depending on experience.
Health Benefits:
Comprehensive health insurance to keep you and your family covered.
Generous Time Off:
Accrue 10 days of vacation in your first year.
Generous Time Off:
The company shuts down for statutory holidays.
Purpose‑Driven Work:
Be part of a team that is dedicated to creating environmentally responsible cleaning solutions.
Inclusive Culture:
We foster a collaborative, inclusive, and innovative workplace where your ideas matter.
How To Apply
We’d love to hear from you if you’re looking for an opportunity to contribute to a dynamic team! Apply today!
Seniority level
Entry level
Employment type
Full‑time
Job function
Quality Assurance
Industries
Chemical Manufacturing
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Job Overview The Quality Assurance Coordinator is responsible for overseeing quality control and quality assurance processes to ensure all manufactured products meet established quality, safety, and regulatory requirements. This role works closely with laboratory and operations teams to support compliance with
FDA regulations ,
cGMP , and
ISO standards , while driving continuous improvement across quality systems. The Coordinator is responsible for SOP implementation, quality documentation, laboratory and testing oversight, and regulatory readiness, ensuring consistent, accurate, and compliant manufacturing operations.
Key Responsibilities
Own, author, review, and maintain
Standard Operating Procedures (SOPs)
and quality documentation
Enforce SOP compliance across production and operations
Support and maintain the
Quality Management System (QMS)
Perform and oversee
basic chemical handling and quality control testing
Lead and support
internal audits
and preparation for
external audits
(FDA, ISO, customer)
Ensure ongoing compliance with
FDA regulations
and
ISO standards
(ISO 9001 or similar)
Coordinate corrective and preventive actions (CAPA) and root‑cause investigations
Train employees on SOPs, quality standards, and compliance requirements
Act as a primary point of contact for quality‑related issues and continuous improvement initiatives
Qualifications
3+ years of experience in
Quality Assurance
within a regulated manufacturing environment
Strong experience with
FDA‑regulated operations
Working knowledge of
ISO standards
(ISO 9001 or similar)
Hands‑on experience with
SOP authoring, enforcement, and documentation control
Experience with
basic chemical handling
and
quality control testing
Ability to work
independently and proactively
in an on‑site manufacturing setting
Strong written and verbal communication skills
Preferred Qualifications
Experience in
chemical manufacturing
or related industries
Experience leading or supporting regulatory and customer audits
CAPA, deviation investigation, and root‑cause analysis experience
Quality certifications (ASQ, ISO Auditor, Lean, Six Sigma)
Why you’ll love working here
Competitive Pay:
Starting salary of $55,000‑$63,000, depending on experience.
Health Benefits:
Comprehensive health insurance to keep you and your family covered.
Generous Time Off:
Accrue 10 days of vacation in your first year.
Generous Time Off:
The company shuts down for statutory holidays.
Purpose‑Driven Work:
Be part of a team that is dedicated to creating environmentally responsible cleaning solutions.
Inclusive Culture:
We foster a collaborative, inclusive, and innovative workplace where your ideas matter.
How To Apply
We’d love to hear from you if you’re looking for an opportunity to contribute to a dynamic team! Apply today!
Seniority level
Entry level
Employment type
Full‑time
Job function
Quality Assurance
Industries
Chemical Manufacturing
#J-18808-Ljbffr