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Hourly Qc Stability Jobs (NOW HIRING)

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 ...

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 ...

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

Title: QC Stability Study Coordinator I Summary * With limited supervision, QC Stability Study Coordinator, is responsible for the oversight of stability program management in accordance with cGMP ...

Quality Control Lab Technician III

Rensselaer, NY · On-site

$19.50 - $24.75/hr

Provide stability summaries for annual product review and stability data for regulatory filings * Serve as designee for the Quality Control Manager as needed * Review documentation, analytical ...

Provide stability summaries for annual product review and stability data for regulatory filings * Serve as designee for the Quality Control Manager as needed * Review documentation, analytical ...

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes ...

Oversees departmental planning and execution, including scheduling, planning, and prioritization of daily work and the QC Stability Program. * Participates with technical support issues and ...

Oversees departmental planning and execution, including scheduling, planning, and prioritization of daily work and the QC Stability Program. * Participates with technical support issues and ...

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Hourly Qc Stability information

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How much do hourly qc stability jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for hourly qc stability in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Hourly Qc Stability vs Hourly Qc Analyst?

AspectHourly Qc StabilityHourly Qc Analyst
CredentialsTypically requires a high school diploma or equivalent, with on-the-job trainingRequires a degree in science or related field, often with certifications in quality control
Work EnvironmentLaboratory or manufacturing settings, repetitive tasksLaboratory or production environments, analytical work
Industry UsageCommon in manufacturing, pharmaceuticals, food productionUsed in similar industries, often with more analytical responsibilities

Hourly Qc Stability focuses on maintaining product stability over time, often with less formal education. Hourly Qc Analyst involves more analytical testing and requires relevant scientific credentials. Both roles are vital in quality control but differ in complexity and qualifications.

More about Hourly Qc Stability jobs
What cities are hiring for Hourly Qc Stability jobs? Cities with the most Hourly Qc Stability job openings:
What are the most commonly searched types of Qc Stability jobs? The most popular types of Qc Stability jobs are:
What states have the most Hourly Qc Stability jobs? States with the most job openings for Hourly Qc Stability jobs include:
Infographic showing various Hourly Qc Stability job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 47% Full Time, 48% Part Time, 1% Temporary, and 3% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
QC Stability Coordinator

QC Stability Coordinator

Lonza

Tampa, FL • On-site

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Posted 8 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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