Top 17 Cosmetic chemistry Jobs in Florida

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
Lab Technician - II
VIVA MFG, LLC. —Tampa, FL
- $22 - $25 an hour
- Weekends as needed
- Mid-level
- Data entry
- Cleaning
- Health insurance
- Dental insurance
Quick Apply
5d
Personal Care Regulatory and R&D Manager
Restem Group Inc. / thebiobox LLC —Miami, FL
- $73,500 - $75,000 a year
- Full-time
- Background check
- 5 years
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
Junior Formulator
C9 Staff —Saint Petersburg, FL
- Monday to Friday
- ERP systems
- Entry level
Quick Apply
R & D Technician
ESTYLE CORP LLC —Jacksonville, FL
- Mid-level
- Organizational skills
- Cleaning
Quality Manager OTC Skincare and Feminine Hygiene
Medical Group Care —Naples, FL
- $120,000 - $130,000 a year
- Full-time
- 5 years
- Mid-level
- Bachelor's degree
Quick Apply
Innovative Senior Formulating Chemist
Cosmetic Solutions —Boca Raton, FL
- Full-time
- 7 years
- Bachelor of Science
- Bachelor's degree
Quick Apply
Operations Technician
Darmerica —Davie, FL
- $48,000 - $55,000 a year
- Email
- Background check
- Microsoft Excel
- Inventory management
- Health insurance
- Paid time off
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Per Diem Traffic Associate (Sampler)
Certified Group —Miami, FL
- Part-time
- Clean driving record
- High school diploma or GED
- Driver's License
- Travel reimbursement
- Mileage reimbursement
Quick Apply
Quality Control Lab Technician
Cosmetic Solutions —Boca Raton, FL
- Full-time
- Mid-level
- Analysis skills
- Organizational skills
Quick Apply
QC
BPW Lab —Hialeah, FL
- From $24.30 an hour
- Full-time
- ERP systems
- English
- Analysis skills
Quick Apply
QC Manager - IC Lab
OXYGEN DEVELOPMENT L L C —Palm Springs, FL
- Full-time
- 6 years
- Customer service
- Word processing
Quick Apply
Regulatory Affairs and Compliance Specialist
CAC —Ormond Beach, FL
- From $35,000 a year
- Full-time
- Background check
- Bachelor's degree
- US work authorization
- Health insurance
- Dental insurance
Quick Apply
3d
Laboratory Analyst I (Wet Chemistry) - Eurofins Drinking Water & Wastewater Southeast - Orlando (Altamonte Springs) FL
Eurofins USA Environment Testing —Altamonte Springs, FL
- $18 an hour
- Full-time
- Bachelor of Science
- Basic math
- English
- Paid holidays
- Disability insurance
Quick Apply
PROJECT MANAGER III
FORMULATED Solutions LLC —Largo, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Engineering
10d
Contract Marine Detailing Specialist - Palmetto Market
Full Throttle Marine —Palmetto, FL
- $12 - $18 an hour
- Choose your own hours
- In person
- Clean driving record
- Surgery
- Mid-level
- Flexible schedule
Quick Apply

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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
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

cosmetic chemistry jobs in florida

Director of Quality and Regulartory Affairs

Lab Technician - II

Personal Care Regulatory and R&D Manager

Junior Formulator

R & D Technician

Quality Manager OTC Skincare and Feminine Hygiene

Innovative Senior Formulating Chemist

Operations Technician

Per Diem Traffic Associate (Sampler)

Quality Control Lab Technician

QC

QC Manager - IC Lab

Regulatory Affairs and Compliance Specialist

Laboratory Analyst I (Wet Chemistry) - Eurofins Drinking Water & Wastewater Southeast - Orlando (Altamonte Springs) FL

PROJECT MANAGER III

Contract Marine Detailing Specialist - Palmetto Market

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