Top 294 Quality assurance Jobs in Clearwater, Fl

Director of Quality and Regulartory Affairs
VIVA MFG, LLC. —Tampa, FL
- $150,000 - $180,000 a year
- Full-time
- 7 years
- Laboratory experience
- Master's degree
- Health insurance
- Dental insurance
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7d
Lab Technician - II
VIVA MFG, LLC. —Tampa, FL
- $22 - $25 an hour
- Weekends as needed
- Mid-level
- Data entry
- Cleaning
- Health insurance
- Dental insurance
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7d
Lab Technician
World Product Solutions —Oldsmar, FL
- $17 - $19 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Math
- Health insurance
- Dental insurance
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Manufacturing Quality Engineer
Genuine Search Group —Holiday, FL
- $80,000 - $90,000 a year
- Full-time
- Mid-level
- In-person
- Manufacturing
- Relocation assistance
- Health insurance
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Software QA Analyst - P&C Background
Robert Half —Saint Petersburg, FL
- Mid-level
- 3 years
- Quality control
- Disability insurance
- Dental insurance
Quick Apply
4d
Inventory & Quality Control Associate
CGS —Clearwater, FL
- From $20 an hour
- Part-time
- Warehouse
- Organizational skills
- In-person
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6d
QA System Specialist
Eagle Labs, Inc —Seminole, FL
- Full-time
- English
- Mid-level
- Databases
- Health insurance
- Dental insurance
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Quality Engineer I
Honeywell Aerospace —Clearwater, FL
- Full-time
- Continuous improvement
- Recruiting
- Entry level
4d
Software Tester
Focus School Software —Saint Petersburg, FL
- Remote
- Mid-level
- SQL
- Paid holidays
- Disability insurance
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Quality Assurance Tester
Heritage Insurance —Tampa, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Opportunities for advancement
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Quality Assurance Associate
Catalent —Saint Petersburg, FL
- Email
- Microsoft Excel
- 3 years
- High school diploma or GED
- Paid holidays
- Health insurance
13d
Testing Purposes Only* Role
DSM - Demo Company —Tampa, FL
- $20 an hour
- Contract
- Remote
- Software development
- Communication skills
- Entry level
- Flexible schedule
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Entry Level Lab Assistant
LabX Diagnostic Systems —Tampa, FL
- $18 an hour
- Full-time
- No experience needed
- Entry level
- Health insurance
- Dental insurance
Quick Apply
Quality Assurance Analyst
VISTRUE LLC —Oldsmar, FL
- Full-time
- Hybrid work
- Microsoft Excel
- Writing skills
- English
Quick Apply
Receiving Inspector- 1st shift
GE Aerospace —Clearwater, FL
- Full-time
- 18 years or older
- Computer literacy
- Pass drug screening
Product Quality Inspector - 1st Shift (onsite)
Collins Aerospace —Largo, FL
- Full-time
- Military
- Mid-level
- High school diploma or GED
- Paid holidays
- Loan repayment program
DCM Quality Analyst - Clearwater, FL
INTREPID STAFFING SERVICES LLC —Clearwater, FL
- Weekends as needed
- Computer Science
- Mid-level
- 3 years
2d
Supplier Quality Engineer II
Honeywell Aerospace —Clearwater, FL
- Full-time
- Mid-level
- Recruiting
Quality Assurance Representative
Gate Group —Tampa, FL
- $66,000 - $68,000 a year
- Full-time
- Bilingual
- Microsoft Excel
- ServSafe
- Commuter assistance
- Disability insurance
Quality Analyst
Integrity Marketing Group —Clearwater, FL
- Full-time
- Mid-level
- Windows
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply

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quality assurance jobs near clearwater, fl

Director of Quality and Regulartory Affairs

VIVA MFG, LLC.
Tampa, FL

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Job Details

Full-time
$150,000 - $180,000 a year
7 days ago

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance

Qualifications

Food and beverage product quality management
FDA submissions
Food safety management
Safety regulations
Drug regulation
Compliance audits & assessments
Collaborating with government agencies
Quality control audit
Manufacturing facility experience
Bachelor's degree
HACCP
Quality assurance experience within pharmaceutical industry
Regulatory/legal compliance standards in production
Productivity software
Cross-functional team management
Cross-functional communication
Supplier quality assurance (SQA)
Senior leadership
Pharmaceutical manufacturing facility experience

Full Job Description

Summary/Overview

The Director of Quality & Regulatory Affairs is responsible for ensuring that all products

manufactured at the facility meet regulatory, quality, and safety standards. This role leads the development, implementation, and oversight of the Quality Management System (QMS), ensuring compliance with cGMP requirements (21 CFR Part 111), NSF/ANSI 455-2 standards, and applicable FDA, state, and international regulations.

The Director partners with Production, R&D, Supply Chain, and senior leadership to align quality initiatives with company goals, drive continuous improvement, and safeguard the integrity of products throughout their lifecycle.

Position Responsibilities

1. Quality System Leadership

a. Lead the design, implementation, and continuous improvement of the Quality Management System to meet 21 CFR Part 111 and NSF/ANSI 455-2 requirements.

b. Ensure readiness for FDA inspections, third-party audits, and customer audits by maintaining a culture of compliance.

c. Take appropriate actions to ensure the integrity of the Quality System, including risk assessments and CAPA (Corrective and Preventive Actions).

d. Oversee the maintenance of all FDA & state licenses, registrations, and regulatory filings.

2. Regulatory Affairs

a. Ensure compliance with applicable FDA regulations, dietary supplement labeling laws, and international regulatory requirements.

b. Collaborate with R&D and marketing to review labels, claims, and formulations for regulatory compliance.

c. Serve as the point of contact for government and regulatory agencies, managing all correspondence, reporting, and audit responses.

d. Maintain current knowledge of changes to relevant laws, regulations, and industry guidance.

e. Partner with customers to support their stability programs, shelf-life verification, and other regulatory needs.

3. Auditing & Verification

a. Develop and oversee internal audit programs to verify compliance with prerequisite programs and SOPs.

b. Review and approve Batch Production Records (BPRs) for accuracy and compliance prior to release .

c. Audit laboratory test results and maintain Certificates of Analysis (COAs) for all products.

d. Oversee third-party laboratory relationships, ensuring timely and accurate testing for raw materials and finished goods.

4. Documentation & SOPs

a. Lead the development, approval, and maintenance of Standard Operating Procedures (SOPs) for production, quality, and regulatory functions.

b. Manage change control processes for formulas, Master Manufacturing Records (MMRs), and controlled documents .

c. Ensure proper documentation of deviations, non-conformances, and investigations.

d. Create and maintain in-process and finished product specifications in collaboration with R&D.

5. Training & Development

a. Establish training programs to ensure all employees are competent to perform functions affecting product safety and quality .

b. Conduct cGMP, HACCP, and regulatory compliance training for Quality, Production, and cross-functional teams.

c. Coach and develop direct reports, building strong leadership within QA/QC and regulatory teams.

6. Cross-Functional Collaboration

a. Partner with R&D to support new product development, including formulation reviews, MMR creation, and product launches.

b. Work closely with Production and Supply Chain to ensure timely material release, production scheduling, and compliance with customer requirements .

c. Act as a liaison between Quality and business stakeholders, ensuring alignment on deadlines and deliverables.

7. Continuous Improvement

a. Monitor key performance indicators (KPIs) related to quality and regulatory performance.

b. Implement continuous improvement initiatives to reduce defects, improve compliance, and streamline processes.

c. Leverage technology such as DataNinja or ERP/QMS platforms for digital batch records, label control, and quality reporting.

Minimum Qualifications

Education: Bachelor’s degree in Chemistry, Microbiology, Life Sciences, Regulatory Affairs, or a related field (Master’s preferred)

Experience:

1. Minimum 7-10 years of experience in dietary supplement, pharmaceutical, food, or cosmetic manufacturing, with at least 5 years in Quality or Regulatory leadership roles .

2. Demonstrated success managing FDA and third-party audits, regulatory submissions, and cross-functional teams.

3. Hands-on experience with cGMP-compliant manufacturing, product labeling regulations, and supplier qualification

Knowledge, Skills and Abilities:

1. Strong understanding of 21 CFR Parts 111, 117, 210, and 211, as well as HACCP and NSF/ANSI 455-2.

2. Proficient in Microsoft Office Suite and familiar with ERP/QMS platforms such as DataNinja.

3. Excellent leadership, interpersonal, and problem-solving skills with the ability to coach teams and drive compliance.

4. Strong written and verbal communication skills for regulatory submissions and cross-functional collaboration.

Certification or License:

1. ASQ Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE).

2. Preventive Controls Qualified Individual (PCQI).

3. Better Process Control School (BPCS) certification.

Pay: $150,000.00 - $180,000.00 per year

Benefits:

Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

quality assurance jobs in clearwater, fl

Director of Quality and Regulartory Affairs

Lab Technician - II

Lab Technician

Manufacturing Quality Engineer

Software QA Analyst - P&C Background

Inventory & Quality Control Associate

QA System Specialist

Quality Engineer I

Software Tester

Quality Assurance Tester

Quality Assurance Associate

Testing Purposes Only* Role

Entry Level Lab Assistant

Quality Assurance Analyst

Receiving Inspector- 1st shift

Product Quality Inspector - 1st Shift (onsite)

DCM Quality Analyst - Clearwater, FL

Supplier Quality Engineer II

Quality Assurance Representative

Quality Analyst

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