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Quality Control Stability Manager Jobs (NOW HIRING)

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

  • Medical

  • Dental

  • Vision

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.

Vaxcyte

Stability Manager

San Carlos, CA

$147K - $171K/yr

Primary responsibility will include managing stability studies for individual projects and ... This individual will collaborate with QC members in a highly collaborative and cross-functional ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

Primary responsibility will include managing stability studies for individual projects and ... This individual will collaborate with QC members in a highly collaborative and cross-functional ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

With limited supervision, QC Stability Study Coordinator, is responsible for the oversight of stability program management in accordance with cGMP regulations. * These duties include execution of ...

Avid Bioservices

Specialist, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Your Role: The Quality Control Specialist is an individual contributor who works within the QC ... Generate weekly stability status reports for management using Excel * Independently manage ...

Herbalife

Manager, Stability

Torrance, CA · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Serve as a primary communication lead for stability, proactively updating project teams, QC managers, R&D, Regulatory, and regional stakeholders on study status, milestones, risks, and outcomes.

Herbalife

Manager, Stability

Torrance, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... QC managers, R&D, Regulatory, and regional stakeholders on study status, milestones, risks, and outcomes. • Ensure stability timelines are met by actively tracking deadlines, stability pull ...

Stoke Therapeutics

Senior Manager, Quality Control

Bedford, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This individual will also lead stability transfers of products including sample chain of custody ... The Sr. Manager, QC is accountable for regulatory inspection interactions related to analytical ...

Kelly Services

QC LCM / Stability Lead

Raleigh, NC

$98K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

QC LCM / Stability Lead Location: Raleigh, NC Salary: $98,000-$138,000/year Schedule: Fully onsite ... Lead analytical method validation, verification, transfer, and lifecycle management activities.

Herbalife

Manager, Stability

Torrance, CA · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... QC managers, R&D, Regulatory, and regional stakeholders on study status, milestones, risks, and outcomes. • Ensure stability timelines are met by actively tracking deadlines, stability pull ...

Novartis

Senior Expert Stability

East Hanover, NJ · On-site

$118K/yr

  • Medical

  • Retirement

  • PTO

Data management to support the Stability Programs including the administration and distribution of Quality Control (QC) stability samples, associated document coordination, and collection and ...

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How much do quality control stability manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for quality control stability manager 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.
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Quality Control Stability Manager jobs near you
Infographic showing various Quality Control Stability Manager job openings in the United States as of August 2026, with employment types broken down into 62% Full Time, 25% Contract, and 13% Nights. Highlights an 100% In-person job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

QC Stability Coordinator

Lonza

Tampa, FL • On-site

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Re-posted 2 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th 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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