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Qc Stability Jobs in Florida (NOW HIRING)

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 sciences operating across five continents. While we work in science, there's no magic formula to how we ...

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 sciences operating across five continents. While we work in science, there's no magic formula to how we ...

Noven Pharmaceuticals

Quality Control Coordinator

Miami, FL · On-site

$19 - $26/hr

Participate in daily QC "Go Meetings" * Ensure timely testing of all laboratory samples * Ensure ... Additional responsibilities may involve stability support/sample logistics and LIMS. * Communicates ...

Noven Pharmaceuticals

Quality Control Coordinator

Miami, FL

$19 - $26/hr

Participate in daily QC "Go Meetings" * Ensure timely testing of all laboratory samples * Ensure ... Additional responsibilities may involve stability support/sample logistics and LIMS. * Communicates ...

New

Noven Pharmaceuticals

Quality Control Coordinator

Miami, FL

$19 - $26/hr

Participate in daily QC "Go Meetings" * Ensure timely testing of all laboratory samples * Ensure ... Additional responsibilities may involve stability support/sample logistics and LIMS. * Communicates ...

Vetio Animal Health

Be Seen First

Quality Control Lab Supervisor

Jupiter, FL · On-site

$75K - $85K/yr

The Quality Control Supervisor/Chemist is a supervisory role for Quality Control Department ... Maintain the Stability Program. Oversight and hands-on testing shall include but not be limited to ...

LARSON CANDO INC

Quality Control Manager

Tamarac, FL · On-site

The Quality Control Manager ensures that all maintenance, repair, and overhaul (MRO) activities ... Stability - Pride in being part of a long-standing, respected aviation organization. * Work-Life ...

LARSON CANDO INC

Quality Control Manager

Tamarac, FL · On-site

The Quality Control Manager ensures that all maintenance, repair, and overhaul (MRO) activities ... Stability - Pride in being part of a long-standing, respected aviation organization. * Work-Life ...

CRH

Quality Control Tech

Branford, FL · On-site

$20/hr

Quality Control Tech Americas Cement Branford, Florida, United States Job ID: 526200 Ash Grove ... We provide stability and advancement opportunities across North America. Use our tuition ...

CRH

Quality Control Tech

Branford, FL

$20/hr

Quality Control Tech Reports to: Site Manager Shift: Varies Pay: $20.00/hr At Ash Grove Cement ... We provide stability and advancement opportunities across North America. Use our tuition ...

AVEVA DRUG DELIVERY SYSTEMS INC

QC Analyst III

Miramar, FL · On-site

$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 ...

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All JobsQc Stability JobsQc Stability Jobs in Florida

Qc Stability information

See Florida salary details

$22.8K

$60.8K

$96.8K

How much do qc stability jobs pay per year?

As of Aug 7, 2026, the average yearly pay for qc stability in Florida is $60,772.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,200.00 and $74,700.00 per year, depending on experience, location, and employer.

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.

What are the key skills and qualifications needed to thrive in the QC Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What is a QC Stability?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

What are popular job titles related to Qc Stability jobs in Florida? For Qc Stability jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Qc Stability jobs in Florida look for? The top searched job categories for Qc Stability jobs in Florida are:
Qc Stability jobs near you
Infographic showing various Qc Stability job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 11% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $60,772 per year, or $29.2 per hour.

QC Stability Coordinator

Lonza

Tampa, FL • On-site

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Re-posted 19 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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