Top 3198 Pharmaceutical 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
4d
Process Development Scientist
Confidential —West Palm Beach, FL
- $75,000 - $120,000 a year
- Full-time
- Doctor of Philosophy
- Travel
- In-person
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Lab Technician
Confidential —West Palm Beach, FL
- $50,000 a year
- Full-time
- Mid-level
- Continuous improvement
- Organizational skills
- Paid time off
- Flexible schedule
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Territory Sales Rep – BioPharma
Prism Biotech —Jacksonville, FL
- $87,650 - $120,872 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
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Pharmaceutical Field Sales Representative
Inizio Engage —Boca Raton, FL
- $63,000 - $117,000 a year
- Full-time
- Background check
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
3h
QA Associate I - PR
AVEVA DRUG DELIVERY SYSTEMS INC —Tamarac, FL
- $50,000 - $65,000 a year
- Bachelor of Science
- ERP systems
- English
Clinical Research Assistant/Pharmacy Tech
Cardiovascular Associates of America —Daytona Beach, FL
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Mid-level
Quick Apply
4d
CLINICAL RESEARCH COORDINATOR I
Moffitt Cancer Center —Land O' Lakes, FL
- $25.68 - $39.16 an hour
- Full-time
- Hybrid work
- Psychology
- Business Administration
- Business
- Paid training
- Relocation assistance
10d
Pharmacy Technician - Refill Calls
Shields Health Solutions —Miami, FL
- $19 - $22 an hour
- Overtime
- Remote
- Microsoft Outlook
- High school diploma or GED
- Communication skills
- Paid parental leave
- Paid holidays
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Non-Acute Pharmaceutical Sales Representative
Cardinal Health —Florida
- $57,000 - $81,600 a year
- Remote
- Microsoft Outlook
- Mid-level
- Bachelor's degree
- Paid parental leave
- Health savings account
1d
Pharmaceutical Lab Technician
Siemens Healthineers —Dania Beach, FL
- $50,040 - $68,805 a year
- Overtime
- Customer service
- Word processing
- Computer literacy
- Paid training
- Disability insurance
Associate Scientist I
Transpire Bio —Weston, FL
- Computer literacy
- Bachelor of Science
- English
Pharmaceutical Detail Rep
Immune Biopharma —Fort Lauderdale, FL
- $89,418 - $119,218 a year
- Full-time
- Analysis skills
- Experience equivalent to degree accepted
- Communication skills
Quick Apply
Pharmacy Care Representative - Work From Home Florida (Active Pharmacy Technician License Needed)
CVS Health —Florida
- $17.00 - $28.46 an hour
- Overtime
- Remote
- Microsoft Outlook
- Windows
- High school diploma or GED
- Paid holidays
- Health insurance
Pharmaceutical Sales - Associate Territory Manager - Kissimmee CMH
Eli Lilly —Orlando, FL
- $63,000 - $151,800 a year
- Full-time
- Bilingual
- Clean driving record
- Mid-level
- Health insurance
- Dental insurance
Pharmaceutical Rep
Access Pharmaceutical —Fort Lauderdale, FL
- Organizational skills
- Leadership
- Communication skills
Quality Assurance Associate
Transpire Bio —Weston, FL
- Mid-level
- 3 years
- Bachelor's degree
Associate Scientist I
Transpire BIO Inc. —Weston, FL
- Computer literacy
- Bachelor of Science
- English
Quick Apply
R & D Technician
ESTYLE CORP LLC —Jacksonville, FL
- Mid-level
- Organizational skills
- Cleaning
QA System Specialist
Eagle Labs, Inc —Seminole, FL
- Full-time
- English
- Mid-level
- Databases
- Health insurance
- Dental insurance
Quick Apply

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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
4 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

pharmaceutical jobs in florida

Director of Quality and Regulartory Affairs

Process Development Scientist

Lab Technician

Territory Sales Rep – BioPharma

Pharmaceutical Field Sales Representative

QA Associate I - PR

Clinical Research Assistant/Pharmacy Tech

CLINICAL RESEARCH COORDINATOR I

Pharmacy Technician - Refill Calls

Non-Acute Pharmaceutical Sales Representative

Pharmaceutical Lab Technician

Associate Scientist I

Pharmaceutical Detail Rep

Pharmacy Care Representative - Work From Home Florida (Active Pharmacy Technician License Needed)

Pharmaceutical Sales - Associate Territory Manager - Kissimmee CMH

Pharmaceutical Rep

Quality Assurance Associate

Associate Scientist I

R & D Technician

QA System Specialist

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