Top 279 Test lead Jobs in Tampa 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
Quick Apply
2d
Data Engineer - MDM
Philip Morris International U.S. —Tampa, FL
- $88,000 - $110,000 a year
- Full-time
- 5 years
- Engineering
- SQL
- Commuter assistance
- Health insurance
Software Development Manager
Loggerhead Insurance —Tampa, FL
- Full-time
- Mentoring
- Senior level
- Leadership
- Disability insurance
- Health insurance
Quick Apply
Quality Assurance Engineer
HEALTHPLANONE, LLC —Tampa, FL
- Full-time
- Computer science
- Computer Science
- Writing skills
- Health insurance
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Program Manager/Training Lead
Contact Government Services, LLC —Tampa, FL
- $180,000 - $200,000 a year
- Full-time
- 5 years
- Mid-level
- Supervising experience
- Health insurance
- Dental insurance
Quick Apply
Compliance and Ops Risk Test Lead - Senior Associate
JPMorganChase —Tampa, FL
- Full-time
- Mid-level
- 3 years
- Continuous improvement
- Health insurance
- Tuition reimbursement
5d
Domain Tech Lead — Infrastructure Patching Automation (Mainframe & AS/400)
Deloitte —Tampa, FL
- $134,000 - $265,000 a year
- Full-time
- 7 years
- Azure
- Up to 50% travel
1d
STINGRAI Test & Evaluation (T&E) Engineer (Engineer Test 2)
HII —Tampa, FL
- $69,451 - $135,000 a year
- Email
- 6 years
- Mid-level
- Master's degree
- Paid holidays
- Health insurance
13d
Senior Product Manager - Infrastructure Services, Smart Build
Equinix —Tampa, FL
- $136,000 - $245,000 a year
- Full-time
- Research
- Office
- Bachelor's degree
- Paid holidays
- Health insurance
5d
Lead Quality Engineer
ClearlyAgile —Tampa, FL
- Contract
- Remote
- APIs
- Senior level
- 2 years
- Paid training
- Paid holidays
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TECHNICAL LEAD L1
Wipro Limited —Tampa, FL
- $60,000 - $135,000 a year
- Pass drug screening
- 8 years
- AWS
- Disability insurance
- Health insurance
QA Lead — Automation & Quality Engineering - VP
Information Technology Senior Management Forum —Tampa, FL
- $113,840 - $170,760 a year
- Full-time
- Office
- Java
- Analysis skills
- Paid holidays
- Disability insurance
Oracle Utilities CSS and WACS Test Lead
Accenture —Saint Petersburg, FL
- $87,400 - $266,300 a year
- Full-time
- Hybrid work
- Oracle
- 5 years
- Office
- Paid holidays
- Disability insurance
OMS Applications Lead
TRC Companies, Inc. —Tampa, FL
- $133,806.40 - $174,866.00 a year
- Full-time
- Computer Science
- Travel
- Senior level
- Paid holidays
- Disability insurance
Director of Product - Ashley Digital
Resident Home —Tampa, FL
- $135,000 - $165,000 a year
- Office
- 8 years
- Analysis skills
- Health savings account
- Dental insurance
Technology Product Management Senior Lead Analyst - Senior Vice President
Information Technology Senior Management Forum —Tampa, FL
- $153,600 - $230,400 a year
- Full-time
- Office
- Master's degree
- AWS
- Paid holidays
- Disability insurance
Testing Lead
Avalon Administrative Services LLC —Tampa, FL
- Full-time
- Customer service
- HIPAA
- Analysis skills
Quick Apply
Quality Analyst
Vevey Software Solutions —Tampa, FL
- Full-time
- AutoCAD
- Computer Science
- Mid-level
Oracle Utilities CSS and WACS Test Lead
Logic —Saint Petersburg, FL
- $87,400 - $266,300 a year
- Full-time
- Hybrid work
- Oracle
- 5 years
- Office
- Paid holidays
- Disability insurance
Database Administrator
Epiq Systems, Inc. —Tampa, FL
- $95,000 - $115,000 a year
- Full-time
- Remote
- Computer Science
- 5 years
- HIPAA

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Director of Quality and Regulartory Affairs

VIVA MFG, LLC.
Tampa, FL

Quick Apply

Job Details

Full-time
$150,000 - $180,000 a year
2 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

test lead jobs in tampa fl

Director of Quality and Regulartory Affairs

Data Engineer - MDM

Software Development Manager

Quality Assurance Engineer

Program Manager/Training Lead

Compliance and Ops Risk Test Lead - Senior Associate

Domain Tech Lead — Infrastructure Patching Automation (Mainframe & AS/400)

STINGRAI Test & Evaluation (T&E) Engineer (Engineer Test 2)

Senior Product Manager - Infrastructure Services, Smart Build

Lead Quality Engineer

TECHNICAL LEAD L1

QA Lead — Automation & Quality Engineering - VP

Oracle Utilities CSS and WACS Test Lead

OMS Applications Lead

Director of Product - Ashley Digital

Technology Product Management Senior Lead Analyst - Senior Vice President

Testing Lead

Quality Analyst

Oracle Utilities CSS and WACS Test Lead

Database Administrator

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