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Quality Control Stability Analyst Jobs in Florida

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... Strong analytical skills with the ability to interpret data and identify trends. * Ability to ...

Lonza

QC Stability Coordinator

Tampa, FL

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... Strong analytical skills with the ability to interpret data and identify trends. * Ability to ...

VIVEX BIOLOGICS INC

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. The QCA ...

VIVEX Biologics, Inc.

Quality Control Analyst

Miami, FL · On-site

$23 - $30.75/hr

Job purpose The Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. The QCA ...

AVEVA DRUG DELIVERY SYSTEMS INC

QC Analyst III

Miramar, FL

$22 - $29.50/hr

* Supports release and stability testing for raw materials, components, standards, intermediate ... Maintains QC compliance systems with guidance of Supervisor * Coordinates testing schedules and ...

AVEVA DRUG DELIVERY SYSTEMS INC

QC Analyst I

Miramar, FL

$22 - $29.50/hr

... QC Miramar. Participates in testing to support Analytical Development method validations ... Job Responsibilities • Supports release and stability testing for raw materials, components ...

Leidos

Quality Control Analyst

Orlando, FL · On-site

$59K - $106K/yr

The Defense Sector of Leidos has a career opportunity for a talented Quality Control Analyst to support a program in the Decision Advantage Business Area. This position serves as a member of a team ...

Noven Pharmaceuticals

QC Analyst II

Miami, FL · On-site

$23 - $30.75/hr

The Analytical QC Analyst II is an integral part of the team, contributing to our success by ... release, stability studies, method transfers, method verifications and investigations.

Unicon Pharma Inc

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

... stability, and request deadlines. Participates in troubleshooting of analytical test methods and ... Quality Control Laboratory environment. Requires working knowledge of cGMP, DEA and other ...

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Quality Control Stability Analyst information

What are Quality Control Stability Analysts?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a Quality Control Stability Analyst, and why are they important?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

What is the difference between Quality Control Stability Analyst vs Quality Control Analyst?

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

Is QC analyst a stressful job?

A Quality Control Stability Analyst role can be stressful due to strict regulatory standards, the need for precision, and tight deadlines. The job often requires attention to detail, analytical skills, and familiarity with laboratory tools, which can contribute to work pressure but also offers a structured environment.

Is QC a high paying job?

Quality Control Stability Analysts typically earn salaries that are competitive within the manufacturing and pharmaceutical industries, with pay often increasing with experience and certifications. While not usually among the highest-paying roles, it can offer a stable income, especially for those with specialized skills or in regulated environments.

What does a quality control analyst do?

A quality control stability analyst monitors and evaluates the stability of pharmaceutical or manufacturing products over time to ensure they meet quality standards. They perform tests, analyze data, and document results, often using laboratory equipment and software, to confirm product consistency and compliance with regulations.

How much is the salary of a QA analyst?

The salary of a Quality Control Stability Analyst typically ranges from $50,000 to $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of laboratory testing, stability studies, and regulatory compliance.

What are some typical challenges faced by Quality Control Stability Analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.
What are popular job titles related to Quality Control Stability Analyst jobs in Florida? For Quality Control Stability Analyst jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability Analyst jobs in Florida look for? The top searched job categories for Quality Control Stability Analyst jobs in Florida are:
What cities in Florida are hiring for Quality Control Stability Analyst jobs? Cities in Florida with the most Quality Control Stability Analyst job openings:
Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in Florida as of July 2026, with employment types broken down into 69% Full Time, 7% Part Time, and 24% Contract. Highlights an 61% Physical, 5% Hybrid, and 34% Remote job distribution.
QC Stability Coordinator

QC Stability Coordinator

Lonza

Tampa, FL • On-site

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Posted 7 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

QC Stability Coordinator
Location: Tampa, FL (on-site)
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
As a QC Stability Coordinator in Tampa, you will play a critical role in managing stability programs that ensure product quality and compliance across development, clinical, and commercial stages.
What you will get
  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • Medical, dental and vision insurance.
  • Opportunities to contribute to meaningful work that improves lives.
  • Career development through cross-functional collaboration and continuous improvement initiatives.
  • The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits

What you will do
  • You will coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
  • You will monitor stability data, identify trends, and escalate out-of-specification or out-of-trend results.
  • You will support audits by preparing documentation and responding to stability-related inquiries.
  • You will manage quality records such as deviations, CAPAs, and change controls within the stability program.
  • You will collaborate with Quality Control, Quality Assurance, and Product Development teams to support study design and execution.
  • You will maintain stability databases, dashboards, and performance metrics to ensure program visibility.
  • You will drive process improvements to enhance efficiency, compliance, and data reliability.

What we are looking for
  • Associate degree or higher in a scientific or related discipline.
  • Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.
  • Knowledge of GMP and stability program requirements, including regulatory guidelines.
  • Strong analytical skills with the ability to interpret data and identify trends.
  • Ability to manage multiple priorities and coordinate activities across teams.
  • Effective communication skills with both technical and non-technical stakeholders.
  • Familiarity with data tools (e.g., Excel) and quality systems is preferred.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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