Skip to main content
Loading
snaprecruit
Logo
Close
Log in
Sign Up
Post a Job

Millions Of Active Candidates

For Employers
VIEW SIMILAR JOBS →
loadingbar
Loading, Please wait..!!

Quality Assurance Specialist

  • Quality Assurance Specialist job type Posted on: Oct 22, 2026
  • Quality Assurance Specialist experience level FrankCrum Staffing, Inc.
  • Quality Assurance Specialist employment type Clearwater, Florida
  • Quality Assurance Specialist employment type Onsite
  • Quality Assurance Specialist salary Full-time
Save this job

Point Apply Here APPLY LATER

Curious about compensation?

Explore the historical salary trends, average pay, and estimated compensation for Quality Assurance Specialist roles in Florida.

View Salary Guide →
Over 12 millions jobs on Snaprecruit.
Find your match !
VIEW SIMILAR JOBS →

Job Title :

Quality Assurance Specialist

Job Type :

Full-Time

Job Location :

Clearwater Florida United States

Remote :

No

Jobcon Logo Job Description :

View Full Description

Job Description

Job Description
Quality Assurance Specialist
Position Summary
The Quality Assurance Specialist is responsible for ensuring product quality, maintaining regulatory compliance, and supporting quality standards throughout the manufacturing process. This role involves inspecting materials and finished products, reviewing production documentation, assisting with audits, and investigating quality issues to ensure compliance with cGMP, FDA, NSF, and other applicable requirements.
The ideal candidate is detail-oriented, organized, and experienced in quality assurance within a manufacturing environment.
Key Responsibilities
  • Conduct inspections of raw materials, packaging materials, in-process production, and finished products.
  • Ensure manufacturing processes comply with cGMP guidelines, FDA regulations, NSF standards, and other applicable quality requirements.
  • Review and maintain batch records, inspection logs, and quality documentation to ensure accuracy and traceability.
  • Identify, document, and investigate quality issues, product deviations, and customer complaints.
  • Assist with corrective and preventive actions (CAPA) to address quality concerns and prevent recurring issues.
  • Support internal and external audits, regulatory inspections, and compliance activities.
  • Monitor manufacturing processes to identify potential quality risks and opportunities for improvement.
  • Collaborate with Production, Research & Development (R&D), and Regulatory teams to resolve quality and compliance issues.
  • Maintain accurate records and ensure quality procedures are followed consistently.
  • Promote continuous improvement and adherence to established quality standards.
Qualifications
  • Previous experience in Quality Assurance or Quality Control, preferably in a manufacturing environment.
  • Knowledge of cGMP guidelines and FDA regulatory requirements.
  • Experience with quality inspections, documentation, audits, and compliance procedures.
  • Strong attention to detail and organizational skills.
  • Ability to investigate issues, identify discrepancies, and support corrective actions.
  • Strong communication and problem-solving skills.
  • Ability to work collaboratively with cross-functional teams.
Preferred Experience
  • Experience with CAPA, deviations, and quality investigations.
  • Familiarity with batch records, manufacturing documentation, and audit preparation.
  • Experience in a regulated manufacturing industry, such as pharmaceuticals, dietary supplements, food, cosmetics, or medical devices.
Ideal Candidate
The ideal candidate is detail-oriented, proactive, and committed to maintaining product quality and regulatory compliance. They should be comfortable reviewing documentation, identifying potential issues, and working with multiple departments to ensure manufacturing standards are consistently met.

#INDSW
 

People Also Search For

Jobcon Logo Position Details

Posted:

Oct 22, 2026

Reference Number:

0b878f2a

Employment:

Full-time

City:

Clearwater

Job Origin:

ziprecruiter

Share this job:

  • linkedin

Jobcon Logo
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!
Get your FREE tickets

Quality Assurance Specialist    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Job Description

Job Description
Quality Assurance Specialist
Position Summary
The Quality Assurance Specialist is responsible for ensuring product quality, maintaining regulatory compliance, and supporting quality standards throughout the manufacturing process. This role involves inspecting materials and finished products, reviewing production documentation, assisting with audits, and investigating quality issues to ensure compliance with cGMP, FDA, NSF, and other applicable requirements.
The ideal candidate is detail-oriented, organized, and experienced in quality assurance within a manufacturing environment.
Key Responsibilities
  • Conduct inspections of raw materials, packaging materials, in-process production, and finished products.
  • Ensure manufacturing processes comply with cGMP guidelines, FDA regulations, NSF standards, and other applicable quality requirements.
  • Review and maintain batch records, inspection logs, and quality documentation to ensure accuracy and traceability.
  • Identify, document, and investigate quality issues, product deviations, and customer complaints.
  • Assist with corrective and preventive actions (CAPA) to address quality concerns and prevent recurring issues.
  • Support internal and external audits, regulatory inspections, and compliance activities.
  • Monitor manufacturing processes to identify potential quality risks and opportunities for improvement.
  • Collaborate with Production, Research & Development (R&D), and Regulatory teams to resolve quality and compliance issues.
  • Maintain accurate records and ensure quality procedures are followed consistently.
  • Promote continuous improvement and adherence to established quality standards.
Qualifications
  • Previous experience in Quality Assurance or Quality Control, preferably in a manufacturing environment.
  • Knowledge of cGMP guidelines and FDA regulatory requirements.
  • Experience with quality inspections, documentation, audits, and compliance procedures.
  • Strong attention to detail and organizational skills.
  • Ability to investigate issues, identify discrepancies, and support corrective actions.
  • Strong communication and problem-solving skills.
  • Ability to work collaboratively with cross-functional teams.
Preferred Experience
  • Experience with CAPA, deviations, and quality investigations.
  • Familiarity with batch records, manufacturing documentation, and audit preparation.
  • Experience in a regulated manufacturing industry, such as pharmaceuticals, dietary supplements, food, cosmetics, or medical devices.
Ideal Candidate
The ideal candidate is detail-oriented, proactive, and committed to maintaining product quality and regulatory compliance. They should be comfortable reviewing documentation, identifying potential issues, and working with multiple departments to ensure manufacturing standards are consistently met.

#INDSW
 

Loading
Please wait..!!