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Validation Manager Jobs in Florida (NOW HIRING)

ZimVie

00 Validation Engineer

Palm Beach Gardens, FL · On-site

Ensure compliance with internal quality management systems and procedures. Collaborate with cross-functional teams to implement and maintain a robust validation program. Requires a bachelor's degree ...

Synchrony Financial

AVP, Model Validation

Lake Mary, FL · On-site

The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations (OCC2011-12/SR 11-7). This role ...

Ankura

Model Validation Director

Tampa, FL · On-site +1

The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

Stem Xpert

GW/Routers Validation Engineer

Tampa, FL · On-site

We strongly believe: " If something cannot be measured, it cannot be managed. " TEKWISSEN measures all of these processes and applies corrective interventions to manage the quality process at its ...

USAA

Lead Model Validator - Fraud

Tampa, FL · Hybrid

Reports validation results and model risk trends/metrics to Enterprise Model Risk Management leadership. * Performs the independent model validation process aligned with the written risk and ...

USAA

Model Validator (Mid-Level) - Fraud/AML

Tampa, FL · Hybrid

$93K - $179K/yr

Produces and delivers validation reports and related validation work to model validation management and model stakeholders. * Executes the independent model validation process compliant with the ...

USAA

Model Validator (Mid-Level) - Fraud/AML

Tampa, FL · Hybrid

$93K - $179K/yr

Produces and delivers validation reports and related validation work to model validation management and model stakeholders. * Executes the independent model validation process compliant with the ...

Ford's Garage

Manager

Fort Myers, FL

Must possess or be able to obtain a valid Manager food safety certification or any other food/alcohol certification, as required by state law Able to stand for 10 hours and lift at least 50 pounds ...

Ford's Garage

Manager

Orlando, FL

Must possess or be able to obtain a valid Manager food safety certification or any other food/alcohol certification, as required by state law Able to stand for 10 hours and lift at least 50 pounds ...

Ford's Garage

Manager

Saint Petersburg, FL

Must possess or be able to obtain a valid Manager food safety certification or any other food/alcohol certification, as required by state law Able to stand for 10 hours and lift at least 50 pounds ...

Ford's Garage

Manager

Cape Coral, FL

Must possess or be able to obtain a valid Manager food safety certification or any other food/alcohol certification, as required by state law Able to stand for 10 hours and lift at least 50 pounds ...

Ford's Garage

Restaurant Manager

Orlando, FL

Must possess or be able to obtain a valid Manager food safety certification or any other food/alcohol certification, as required by state law Able to stand for 10 hours and lift at least 50 pounds ...

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Validation Manager information

See Florida salary details

$35.5K

$78.8K

$119.9K

How much do validation manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for validation manager in Florida is $78,776.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,700.00 and $98,600.00 per year, depending on experience, location, and employer.

How does a Validation Manager typically collaborate with other departments during project execution?

Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.

What is the role of a validation manager?

A validation manager oversees the process of ensuring that products, processes, or systems meet specified requirements and quality standards. They develop validation protocols, coordinate testing activities, and ensure compliance with industry regulations, often working with quality assurance teams and utilizing validation tools. Their role is critical in industries like pharmaceuticals, manufacturing, and healthcare to ensure safety and efficacy.

What job makes $10,000 a month without a degree?

A Validation Manager typically earns a salary that can reach or exceed $10,000 per month, especially with experience and industry expertise. This role involves overseeing validation processes in industries like pharmaceuticals or manufacturing, often requiring strong technical skills and certifications but not necessarily a college degree.

What jobs in the US pay 300,000 a year?

Validation Managers in industries such as pharmaceuticals, biotechnology, and manufacturing can earn salaries approaching or exceeding $300,000 annually, especially with extensive experience, advanced certifications, and leadership responsibilities. High-level roles in finance, law, and executive management also frequently reach or surpass this salary level. Compensation varies based on location, company size, and individual expertise.

What Is a Validation Manager?

A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.

What are the key skills and qualifications needed to thrive as a Validation Manager, and why are they important?

To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.

What jobs pay 500,000 a year in the US?

Validation Managers typically do not earn $500,000 annually; such high salaries are more common in executive roles like CEOs, CFOs, or specialized high-level professionals in finance, law, or technology. Senior executives and certain specialized roles with significant responsibilities and experience can reach or exceed this income level, often including bonuses and stock options. Compensation varies widely based on industry, company size, and geographic location.

What is the difference between Validation Manager vs Quality Assurance Specialist?

AspectValidation ManagerQuality Assurance Specialist
CertificationsGxP, ISO, or industry-specific validation certificationsISO, Six Sigma, or QA-related certifications
Work EnvironmentRegulated industries like pharmaceuticals, biotech, or medical devicesManufacturing, software, or service industries
Primary FocusEnsuring validation processes for equipment, systems, and processes meet standardsMonitoring and improving overall quality processes and compliance

The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.

What are Validation Managers?

Validation Managers are professionals responsible for overseeing and managing the validation processes within an organization, particularly in industries like pharmaceuticals, biotechnology, and manufacturing. Their main role is to ensure that products, equipment, and processes meet regulatory standards and operate consistently as intended. They coordinate validation activities, develop protocols, lead teams, and ensure compliance with quality and safety regulations. Validation Managers play a critical role in maintaining product quality, reducing risks, and ensuring that all procedures meet industry and governmental standards.
More about Validation Manager jobs
What are the most commonly searched types of Validation jobs in Florida? The most popular types of Validation jobs in Florida are:
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What cities in Florida are hiring for Validation Manager jobs? Cities in Florida with the most Validation Manager job openings:
Validation Manager jobs near you
00 Validation Engineer

00 Validation Engineer

ZimVie

Palm Beach Gardens, FL • On-site

Full-time

Posted 2 days ago

Job description

00 Validation Engineer
Location: Palm Beach Gardens, Florida, USA
Function: Engineering
We are ZimVie, a global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients' smiles, function, and confidence. Our company is founded on a legacy of trusted brands, products, and clinical evidence made possible through an inclusive and collaborative culture that empowers our team members to bring their whole selves - their best selves - to work every day to accomplish our Mission. Together, our dedicated, diverse global team is shaping an exciting future for ZimVie - we hope you'll consider being a part of it!
Validation Engineer (Palm Beach Gardens, FL): Develop and execute a comprehensive periodic review program for validated systems and processes, including equipment, software, and manufacturing processes. Conduct thorough reviews of validation documentation, including validation plans, protocols, reports, and change controls. Assess the continued suitability, adequacy, and effectiveness of validated systems and processes. Identify and document potential risks or deviations from established validation requirements. Recommend corrective and preventive actions to address identified issues. Enact measures and reviews to ensure systems, once validated, remain in a validated state throughout their life cycle. Assess the need for revalidation activities or supplemental validation. Stay up to date with relevant regulatory requirements (e.g., FDA, ISO 13485) related to validation and periodic review. Ensure compliance with internal quality management systems and procedures. Collaborate with cross-functional teams to implement and maintain a robust validation program.
Requires a bachelor's degree in mechanical engineering, electrical engineering, a related field, or foreign equivalent. Requires 3 years of experience in job offered or related field.
Requires 3 years of experience with:
  • GxP regulations & state-of-the-art validation techniques used to ensure systems, processes, and equipment that impact product quality and patient safety are consistently compliant and reliable.
  • Development, Implementation, and execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) system protocols for any system that creates, modifies, maintains, or transmits electronic records/data used in manufacturing, quality control, or documentation.
  • Process, equipment and software validation for critical manufacturing processes, automated equipment, and quality-impacting software to prove they consistently meet predetermined specifications including but not limited to equipment such as CNCs, laser markers, packagers, vision systems, ultrasonic cleaning lines, mills, grinders, etc.
  • Manufacturing practices including ISO 13485 and 21CFR820 guidelines used to establish, maintain, and ensure the compliance of the Quality Management System (QMS) for devices sold globally and in the U.S.
  • Utilizing Statistical Process Control (SPC) Tools (e.g., Minitab) used to analyze validation data (especially for Process Performance Qualification, PPQ runs) to demonstrate process capability (Cpk) and statistical justification for acceptance criteria.
  • Utilizing Risk Management Methodology (e.g., ISO 14971) used to formally assess and document risks associated with processes and equipment, which then justifies the scope and rigor of the validation effort.
  • Utilizing Qualityze or Similar QMS Platform used to manage and document all controlled quality records, including Change Controls, Non-Conformances (NCs), and Corrective and Preventive Actions (CAPAs) that often stem from validation activities.

ZimVie is an Equal Opportunity Employer committed to diversity and inclusion in the workplace. All qualified applicants for employment and employment decisions, including hiring, promotion, transfer, demotion, evaluation, compensation, and separation, are considered without regard to race, color, religion, religious beliefs, creed, national origin, ancestry, citizenship status, age, gender/sex (including pregnancy, childbirth, related medical conditions, lactation and breastfeeding), gender identity or expression (including transgender status), sexual orientation, marital status, military status, protected veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any other status protected under applicable federal, state and local laws.
ZimVie generally does not sponsor applicant work visas for this position.
  • Requisition ID: 3517

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