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Quality Control Stability Analyst Jobs (NOW HIRING)

Abzena Inc.

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 ... Drive operational readiness and resource planning to support analytical testing needs. Stability ...

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 ... Strong analytical skills with the ability to interpret data and identify trends. * Ability to ...

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 ... Strong analytical skills with the ability to interpret data and identify trends. * Ability to ...

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 ... These duties include execution of trend analysis, documentation review, support of deviations (OOS ...

TekWissen LLC

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program ... Review analytical data against established acceptance criteria * Perform technical review of peer ...

Curia, Inc.

Quality Control Lab Technician III

Rensselaer, NY · On-site

$19.50 - $24.75/hr

Quality Control Lab Technician III in Rensselaer, NY Build your future at Curia, where our work has ... Analyze data for stability trends and deviations to ensure consistency with historical time points ...

AMRI

Quality Control Lab Technician III

Rensselaer, NY

$19.50 - $24.75/hr

Quality Control Lab Technician III in Rensselaer, NY Build your future at Curia, where our work has ... Analyze data for stability trends and deviations to ensure consistency with historical time points ...

Glenmark Pharmaceuticals

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in ... Provide information, data for evaluation and execution of stability study as per Quality and ...

Cellares

Quality Control Analyst

Bridgewater, NJ

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

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

As of Jul 23, 2026, the average hourly pay for quality control stability analyst in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What are Quality Control Stability Analysts?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a Quality Control Stability Analyst, and why are they important?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

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

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

Is QC analyst a stressful job?

A Quality Control Stability Analyst role can be stressful due to strict regulatory standards, the need for precision, and tight deadlines. The job often requires attention to detail, analytical skills, and familiarity with laboratory tools, which can contribute to work pressure but also offers a structured environment.

Is QC a high paying job?

Quality Control Stability Analysts typically earn salaries that are competitive within the manufacturing and pharmaceutical industries, with pay often increasing with experience and certifications. While not usually among the highest-paying roles, it can offer a stable income, especially for those with specialized skills or in regulated environments.

What does a quality control analyst do?

A quality control stability analyst monitors and evaluates the stability of pharmaceutical or manufacturing products over time to ensure they meet quality standards. They perform tests, analyze data, and document results, often using laboratory equipment and software, to confirm product consistency and compliance with regulations.

How much is the salary of a QA analyst?

The salary of a Quality Control Stability Analyst typically ranges from $50,000 to $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of laboratory testing, stability studies, and regulatory compliance.

What are some typical challenges faced by Quality Control Stability Analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.
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Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 7% Hybrid, and 10% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.
QC Stability Manager

QC Stability Manager

Abzena Inc.

San Diego, CA • On-site

$120K - $150K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
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 standard management across Abzena's biopharmaceutical operations. This role blends scientific expertise, operational leadership, and cross-functional influence - ideal for a seasoned QC leader who thrives in a fast-paced, growth-oriented environment.
Responsibilities
People Leadership & Laboratory Excellence
  • Lead, mentor, and develop QC scientists and associates, fostering a culture of technical excellence, accountability, and continuous improvement.
  • Ensure all personnel are fully trained in technical competencies, cGMP, data integrity, and laboratory safety.
  • Communicate clear goals, priorities, and performance expectations to direct reports.
  • Partner with facilities teams to maintain a state of control for laboratory equipment, including calibration, qualification, and preventive maintenance.
  • Drive operational readiness and resource planning to support analytical testing needs.
Stability Program Ownership
  • Oversee end-to-end stability program management, including study design, protocol development, execution, and lifecycle oversight.
  • Ensure all stability protocols and reports meet ICH, internal SOP, and quality system requirements.
  • Manage sample logistics, material staging, and tracking for all stability studies.
  • Monitor active stability programs, ensuring on-time pulls, testing, reporting, and issuance of Stability Summary Sheets.
  • Maintain accurate, audit-ready stability inventory and documentation.
Reference Standard Strategy & Oversight
  • Lead qualification, lifecycle management, retesting, and documentation for reference standards.
  • Oversee inventory, testing schedules, stability requirements, and timely issuance of certificates.
  • Train and guide laboratory personnel supporting reference standard activities.
  • Represent QC Stability in internal meetings, client interactions, audits, and cross-functional forums.
Quality, Compliance & Technical Support
  • Author or review deviations, investigations, CAPAs, change controls, and risk assessments related to stability and reference standards.
  • Support or lead investigations involving OOS, OOT, non-conformances, and laboratory events.
  • Review analytical data packages, perform data trending, and troubleshoot complex laboratory issues.
  • Collaborate closely with Manufacturing, Analytical Development, Tech Transfer, Regulatory, and Quality Assurance teams.
Strategic Planning & Organizational Growth
  • Contribute to long-term planning for equipment, staffing, and organizational structure.
  • Recommend and justify new equipment, headcount, promotions, and process improvements.

Qualifications
  • Bachelor's degree or higher in Chemistry, Biology, or related Life Sciences discipline.
  • 10+ years of QC experience in GMP pharmaceutical or biotechnology laboratories.
  • 5-6+ years of people management experience in QC laboratory environments.
  • Deep expertise with analytical platforms including HPLC, SDS-PAGE, ELISA, Capillary Electrophoresis, cIEF (Maurice), UV-Vis, cell-based potency assays, and compendial methods.
  • Strong working knowledge of ICH, USP, EP, and FDA guidelines related to method development, validation, and stability studies.

Physical Requirements
  • Frequently lift and or move objects up to 20 pounds.
  • Stand/walk during entire length of shift.
  • Use of arms, hands and fingers to handle, feel or reach.
  • Ability to climb, balance, stoop, kneel, crouch, or crawl.
  • Visual abilities include near and far sight, color, peripheral vision, depth and ability to focus.

$120,000 - $150,000 a year
FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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