Top 78 Quality engineer Jobs in Oldsmar, 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
5d
Quality Assurance Engineer
HEALTHPLANONE, LLC —Tampa, FL
- Full-time
- Computer science
- Computer Science
- Writing skills
- Health insurance
Quick Apply
Mechanical Engineer - Product Quality Manager
WellnessSpace Brands —Clearwater, FL
- Full-time
- 5 years
- Master's degree
- Assembly
- Health insurance
- Dental insurance
Quick Apply
Quality Assurance Engineer
BPI labs (Belcher Pharmaceuticals LLC) —Largo, FL
- Full-time
- Customer service
- Bachelor of Science
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
Sr Supplier Quality Engineer - 29879_M
BEPC Inc —Clearwater, FL
- $47.48 - $50.48 an hour
- Full-time
- 6 years
- Engineering
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Cable & CCA Inspector
Sun Technologies —Oldsmar, FL
- $20 - $28 an hour
- Multiple hires
- Mid-level
- Assembly
- In-person
- Health insurance
- 401(k)
Quick Apply
QA Automation Engineer IV
Hudson Manpower —Florida
- Full-time
- Remote
- Java
- SQL
- Experience equivalent to degree accepted
- Profit sharing
- Paid training
Quick Apply
Quality Engineer - Manufacturing
SolarEdge —Seminole, FL
- Full-time
- Engineering
- Mid-level
- 3 years
Quick Apply
Lead Quality Engineer
ClearlyAgile —Tampa, FL
- Contract
- Remote
- APIs
- Senior level
- 2 years
- Paid training
- Paid holidays
Quick Apply
Quality Engineer I
Honeywell Aerospace —Clearwater, FL
- Full-time
- Continuous improvement
- Recruiting
- Entry level
3d
Software Quality Assurance Engineer
Rooms To Go —Seffner, FL
- Full-time
- Mid-level
- Analysis skills
- US work authorization
- Disability insurance
- Health insurance
2d
Quality Engineer II
Honeywell Aerospace —Clearwater, FL
- Full-time
- Mid-level
1d
Principal, Corporate Quality Engineer
Chromalloy —Oldsmar, FL
- $112,000 - $147,000 a year
- Overtime
- Engineering
- Pass drug screening
- Travel
- Wellness program
- Paid holidays
Quick Apply
2d
QA Engineer
Bridgeway Benefit Technologies —Tampa, FL
- Remote
- Computer Science
- Software troubleshooting
- Java
Quick Apply
Senior Quality Engineer
Honeywell Aerospace —Clearwater, FL
- Full-time
- Manufacturing
- Senior level
Quality Engineer
Compulink Cable Assemblies of Florida, INC —Saint Petersburg, FL
- Engineering
- Analysis skills
- Mentoring
Quick Apply
Quality Engineer II
Saint Gobain —Clearwater, FL
- Mid-level
- Military encouraged
- 2 years
- Wellness program
- Paid parental leave
Quick Apply
4d
Supplier Quality Engineer II
Honeywell Aerospace —Clearwater, FL
- Full-time
- Mid-level
- Recruiting
Program Quality Assurance Engineer II (Project QA)
General Dynamics Ordnance & Tactical Systems —Saint Petersburg, FL
- Full-time
- Up to 50% travel
- Engineering
- Mid-level
- Health insurance
Sr Quality Engineer
West Pharmaceutical Services —Saint Petersburg, FL
- Background check
- Microsoft Excel
- 5 years

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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
5 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 engineer jobs in oldsmar, fl

Director of Quality and Regulartory Affairs

Quality Assurance Engineer

Mechanical Engineer - Product Quality Manager

Quality Assurance Engineer

Sr Supplier Quality Engineer - 29879_M

Cable & CCA Inspector

QA Automation Engineer IV

Quality Engineer - Manufacturing

Lead Quality Engineer

Quality Engineer I

Software Quality Assurance Engineer

Quality Engineer II

Principal, Corporate Quality Engineer

QA Engineer

Senior Quality Engineer

Quality Engineer

Quality Engineer II

Supplier Quality Engineer II

Program Quality Assurance Engineer II (Project QA)

Sr Quality Engineer

I want to receive the latest job alert for quality engineer in oldsmar, fl

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