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Full Time 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 Manager

San Diego, CA · On-site

$120K - $150K/yr

As the QC Stability Manager , you will lead a high-performing Quality Control team responsible for ensuring the integrity, reliability, and regulatory compliance of stability programs and reference ...

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 ...

The Manager, QC Stability provides leadership and strategic oversight of the stability programs from early phase through commercialized programs. This role ensures regulatory compliance, analytical ...

Apply Early

The Manager, QC Stability provides leadership and strategic oversight of the stability programs from early phase through commercialized programs. This role ensures regulatory compliance, analytical ...

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 ...

QC Lab Technician

Cerritos, CA · On-site

$20 - $22/hr

M-F 8am-4:30pm Contract to hire Job Summary We are seeking a full-time QC Laboratory Technician to ... Conduct stability testing on finished products * Monitor production batches to ensure quality ...

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 ...

HOT TOPIC DISTRIBUTION CENTER i s looking to hire a Full-Time QUALITY CONTROL ASSOCIATE directly! Help us cross our T's and dot our I's as a Quality Control Associate within our Tennessee ...

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QC Specialist II-Stability Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 7:00 AM-4:00 PM EST. What you will get: Below you will ...

QC Specialist II-Stability Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 7:00 AM-4:00 PM EST. What you will get: Below you will ...

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Liquid Industrial Coatings QC Technician Full Time (Elgin, IL- First shift) Our client, a specialized Industrial Coatings Manufacturing Company located in Elgin, is seeking a full time (QC) Quality ...

We are seeking a full-time Quality Control (QC) Technician to join our team. As a member of our Engineering department you will help maintain, and support various broadcast equipment for our clients ...

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Full Time Qc Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do full time qc stability jobs pay per year?

As of Jul 6, 2026, the average yearly pay for full time qc stability in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.
More about Full Time Qc Stability jobs
What are the most commonly searched types of Qc Stability jobs? The most popular types of Qc Stability jobs are:
What job categories do people searching Full Time Qc Stability jobs look for? The top searched job categories for Full Time Qc Stability jobs are:
Infographic showing various Full Time Qc Stability job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
QC Stability Coordinator

QC Stability Coordinator

Lonza

Tampa, FL • On-site

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Posted 18 days ago


Lonza rating

8.2

Company rating: 8.2 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

29th of 73 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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