ZipRecruiter

Log In

1

Pharmaceutical Stability Manager Jobs (NOW HIRING)

Lonza

QC Stability Coordinator

Tampa, FL

$18.75 - $25.75/hr

As a QC Stability Coordinator in Tampa, you will play a critical role in managing stability ... Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

As a QC Stability Coordinator in Tampa, you will play a critical role in managing stability ... Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.

Lonza

QC Specialist III-Stability

Portsmouth, NH · On-site

Minimum of 4 years of hands-on experience managing or supporting GMP stability programs within a pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination ...

Lonza

QC Specialist II-Stability

Portsmouth, NH

Minimum of 3 years of hands-on experience managing or supporting GMP stability programs within a pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination ...

next page

Showing results 1-20

People also search for

All JobsPharmaceutical Stability Manager Jobs

Pharmaceutical Stability Manager information

See salary details

$24.5K

$59.5K

$116K

How much do pharmaceutical stability manager jobs pay per year?

As of Jun 11, 2026, the average yearly pay for pharmaceutical stability manager in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a Pharmaceutical Stability Manager when coordinating cross-functional teams during stability studies?

Pharmaceutical Stability Managers often encounter challenges in aligning timelines and expectations among cross-functional teams, such as quality assurance, analytical development, and manufacturing. Effective communication is essential to ensure that sample collection, testing, and documentation happen according to regulatory guidelines. Additionally, managing unexpected results or delays requires strong problem-solving skills and flexibility. Building collaborative relationships and maintaining clear documentation are key to overcoming these challenges and ensuring the success of stability programs.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Stability Manager, and why are they important?

To thrive as a Pharmaceutical Stability Manager, you need a strong background in chemistry or pharmaceutical sciences, experience with stability testing, and a relevant degree (often a BS or MS). Expertise in analytical instruments (such as HPLC and GC), familiarity with LIMS, and knowledge of ICH guidelines or regulatory compliance are typically required. Strong project management, attention to detail, and effective communication skills help in coordinating teams and ensuring data integrity. These skills are crucial for maintaining product quality, ensuring regulatory compliance, and driving successful stability programs.

What are Pharmaceutical Stability Managers?

Pharmaceutical Stability Managers are professionals responsible for overseeing stability studies that ensure the safety, efficacy, and quality of pharmaceutical products throughout their shelf life. They design, implement, and monitor stability testing programs according to regulatory guidelines, analyze results, and prepare documentation for regulatory submissions. Their role is crucial in determining storage conditions and expiration dates for medications, ensuring compliance with industry standards and regulations.
More about Pharmaceutical Stability Manager jobs
What cities are hiring for Pharmaceutical Stability Manager jobs? Cities with the most Pharmaceutical Stability Manager job openings:
What states have the most Pharmaceutical Stability Manager jobs? States with the most job openings for Pharmaceutical Stability Manager jobs include:
What job categories do people searching Pharmaceutical Stability Manager jobs look for? The top searched job categories for Pharmaceutical Stability Manager jobs are:
Pharmaceutical Stability Manager jobs near you

QC Stability Coordinator

Lonza

Tampa, FL

$18.75 - $25.75/hr

Full-time

Medical, Dental, Vision

Posted 23 days ago

Lonza rating

8.1

Company rating: 8.1 out of 10

Based on 40 frontline employees who took The Breakroom Quiz

31st of 71 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.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply