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Assistant Manager, Quality Operation

Kiss Products -
Ellabell, GA

Apply Now

Job Details

Full-time
$15 - $47 an hour
8 days ago

Qualifications

Defect resolution root cause analysis
Quality control statistical data analysis
Preventive action implementation
Statistical Process Control
Corrective and preventive actions (CAPA)
Internal investigations
Quality control audit
Bachelor's degree
Compliance documentation
Leading team collaboration initiatives
Regulatory/legal compliance standards in production
Productivity software
Quality audits
Cross-functional team management
Cross-functional communication
Audit support
Failure analysis

Full Job Description

Job Description Summary:

The QA/QC Assistant Manager is responsible for supporting and maintaining Quality Assurance (QA) and Quality Control (QC) systems to ensure products consistently meet company standards, customer requirements, and regulatory requirements. This role assists in managing quality operations, driving continuous improvement initiatives, overseeing audits and inspections, leading corrective actions, and supporting compliance with industry regulations and quality management systems.
Candidates with experience in the cosmetic industry are strongly preferred. Experience in pharmaceutical manufacturing or GMP-regulated environments is also highly valued.

Job Description:

Key Responsibilities

Quality Assurance & Compliance

Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS).
Ensure compliance with applicable regulatory requirements, company standards, and customer specifications.
Assist in preparing for and coordinating internal, customer, and regulatory audits.
Develop, review, and maintain quality policies, procedures, work instructions, and quality documentation.

Quality Control Operations

Oversee inspection and testing activities for raw materials, packaging materials, in-process products, and finished goods.
Review and approve quality records, inspection reports, and test results.
Monitor product quality trends and identify opportunities for improvement.
Ensure proper calibration and maintenance of laboratory and inspection equipment.

Investigation & Continuous Improvement

Lead investigations related to product non-conformities, deviations, customer complaints, and quality incidents.
Conduct root cause analysis using quality improvement tools and methodologies.
Drive Corrective and Preventive Action (CAPA) processes and verify effectiveness of implemented actions.
Participate in continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction.

Supplier & Customer Quality Management

Support supplier qualification, evaluation, and ongoing quality performance monitoring.
Collaborate with suppliers to address quality issues and implement improvement plans.
Respond to customer quality concerns and support resolution activities.

Leadership & Collaboration

Provide guidance and technical support to QA/QC staff and cross-functional teams.
Support employee training programs related to quality systems, GMP practices, and quality standards.
Promote a culture of quality, compliance, and continuous improvement throughout the organization.

Required Qualifications

Education

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, Industrial Engineering, Quality Management, or a related scientific discipline.

Experience

Minimum 5 years of experience in Quality Assurance, Quality Control, or Quality Management within a manufacturing environment.
Experience supporting quality systems, audits, investigations, and CAPA programs.
Experience leading or coordinating cross-functional quality improvement activities.

Technical Knowledge

Quality Management Systems (QMS)
Root Cause Analysis (5 Why, Fishbone, FMEA)
CAPA Management
Internal and External Audits
Statistical Process Control (SPC)
Regulatory Compliance and Documentation Management
Microsoft Office Applications

Preferred Qualifications

Experience in the cosmetic industry strongly preferred.
Experience in pharmaceutical manufacturing, biotechnology, or GMP-regulated environments preferred.
Knowledge of cosmetic regulations, GMP requirements, and product quality standards.
Experience with ISO 9001, GMP, GLP, or other relevant quality standards.
Supervisory or team leadership experience.
Six Sigma, Lean Manufacturing, or related continuous improvement experience.

Preferred Certifications

Certified Quality Engineer (CQE)
Certified Quality Auditor (CQA)
ISO 9001 Internal Auditor / Lead Auditor
Six Sigma Green Belt or Black Belt
GMP Training or Related Certification

Ideal Candidate Profile

A quality professional with solid experience in cosmetics manufacturing or pharmaceutical/GMP-regulated industries, possessing strong knowledge of quality systems, regulatory compliance, root cause analysis, and continuous improvement methodologies, with the ability to lead quality initiatives and support operational excellence.

Qualification(s):

Education(s):

Work Experience:

Skill(s):

Language(s):

Certification(s):

Not Applicable

The anticipated compensation range is

15.00 - 47.00 USD Hourly

Actual compensation will be determined based on various factors including qualifications, education, experience, and location. The pay range is subject to change at any time dependent on a variety of internal and external factors.

Kiss Nail Products, Inc., KDC GA Corp., Ivy Enterprises, Inc., AST Systems, LLC, Red Beauty, Inc., or Dae Do, Inc. (collectively, the “Company”) is an equal opportunity employer and is committed to a diverse and inclusive workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, or any other characteristic protected by law.

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