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Quality Control Stability Coordinator Jobs (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

$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 ...

Actalent

Stability Coordinator

Mount Prospect, IL · On-site

$32 - $36/hr

Collaborate with Quality Control, Quality Operations, and Quality System for comprehensive report completion. * Provide routine metric reports and status updates on the stability program to the ...

Unicon Pharma Inc.

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 ...

Herbalife

Stability Coordinator

Winston Salem, NC · On-site

The First Shift Stability Coordinator will work onsite at our state of art Innovation and ... Collaborate with Quality, R&D, and Licensing partners to gain insight into specifications and how ...

Herbalife

Stability Coordinator

Winston Salem, NC · On-site

The First Shift Stability Coordinator will work onsite at our state of art Innovation and ... Collaborate with Quality, R&D, and Licensing partners to gain insight into specifications and how ...

Avid Bioservices

Specialist, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

Your Role: The Quality Control Specialist is an individual contributor who works within the QC ... Prepare/aliquot R&D stability samples * Assist in Reference Standard Generation activities

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How much do quality control stability coordinator jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for quality control stability coordinator in the United States is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $26.20 per hour, depending on experience, location, and employer.

What is a quality control stability coordinator?

Quality Control Stability Coordinators are professionals responsible for managing and overseeing stability testing of products, typically in pharmaceutical or biotechnology industries. They ensure that products meet quality and regulatory standards by coordinating stability studies, tracking sample storage, and maintaining documentation. Their work helps determine how long products remain safe and effective under various environmental conditions. They also collaborate with different departments, such as quality assurance and manufacturing, to ensure compliance with regulatory guidelines.

What are the key skills and qualifications needed to thrive as a quality control stability coordinator?

To thrive as a Quality Control Stability Coordinator, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by a bachelor’s degree and experience in quality control or laboratory environments. Familiarity with laboratory information management systems (LIMS), stability testing protocols, and regulatory guidelines such as GMP and ICH is typically required. Attention to detail, organizational skills, and effective communication are crucial soft skills for managing stability studies and collaborating with cross-functional teams. These competencies ensure accurate data management, regulatory compliance, and the reliability of product quality assessments.

What are the main challenges a quality control stability coordinator faces when managing stability studies, and how can they effectively address them?

A Quality Control Stability Coordinator often encounters challenges such as coordinating multiple stability studies simultaneously, ensuring regulatory compliance, and maintaining accurate documentation. Managing timelines and responding to unexpected deviations in product stability can also be demanding. Effective communication with cross-functional teams, meticulous organization, and staying updated on regulatory guidelines help address these challenges. Utilizing robust data management systems and proactively identifying potential risks can further streamline the workflow and ensure the integrity of stability programs.

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

AspectQuality Control Stability CoordinatorQuality Control Analyst
Primary FocusMonitoring product stability and ensuring consistency over timeTesting and analyzing products to ensure quality standards
CertificationsOften requires GMP, GLP, or industry-specific certificationsTypically requires GMP or relevant laboratory certifications
Work EnvironmentLaboratory and manufacturing settings, focusing on stability studiesLaboratory testing, data analysis, and quality assessment
Employer & Industry UsagePharmaceutical, biotech, and manufacturing industriesPharmaceutical, food, and consumer goods industries

The Quality Control Stability Coordinator primarily oversees product stability programs, ensuring products remain effective over time, while the Quality Control Analyst conducts testing and analysis to verify product quality. Both roles require similar certifications and work environments but focus on different aspects of quality assurance.

What cities are hiring for Quality Control Stability Coordinator jobs?

Cities with the most Quality Control Stability Coordinator job openings:

What are the most commonly searched types of Quality Control Stability jobs?

The most popular types of Quality Control Stability jobs are:

What states have the most Quality Control Stability Coordinator jobs?

States with the most job openings for Quality Control Stability Coordinator jobs include:

What are popular job titles related to Quality Control Stability Coordinator jobs?

For Quality Control Stability Coordinator jobs, the most frequently searched job titles are:

Infographic showing various Quality Control Stability Coordinator job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $48,903 per year, or $23.5 per hour.

QC Stability Coordinator

Tampa, FL • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Re-posted 24 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

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.

What Lonza employees say

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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