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Qc Stability Jobs (NOW HIRING)

Abzena Inc.

QC Stability Manager

San Diego, CA · On-site

The QC Stability Manager is responsible for leading and supporting GMP large-molecule stability testing across all phases of client programs within QC. This role provides strategic and operational ...

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 ...

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 ...

Pfizer

QC Stability Operations Specialist

Andover, MA

$68K - $114K/yr

Why Patients Need You The QC Stability Operations Specialist will join and support a diverse Quality Control Laboratory Operations Support (QCLOS) team consisting of Quality Control Stability ...

Genezen

Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

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 ...

Genezen

Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

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 ...

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 ...

Genezen

Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

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 ...

Curia, Inc.

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 ...

AMRI

Quality Control Lab Technician III

Rensselaer, NY

$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 ...

Lonza

QC Specialist II-Stability

Portsmouth, NH · On-site

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 ...

Lonza

QC Specialist II-Stability

Portsmouth, NH

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 ...

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 management in compliance with cGMP regulations, with limited supervision. This role includes ...

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All JobsQc Stability Jobs

Qc Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc stability jobs pay per year?

As of Jun 21, 2026, the average yearly pay for 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.

What jobs in the US pay $300,000 a year?

In the US, high-paying roles related to QC Stability or similar fields often include senior pharmaceutical or biotech quality assurance managers, regulatory affairs directors, or senior research scientists, especially in large companies or with specialized expertise. These positions typically require advanced degrees, extensive experience, and leadership responsibilities, and may involve working in regulated environments with certifications like Six Sigma or GMP compliance.

What career paths are possible in QC?

A QC (Quality Control) professional can advance to roles such as QC Supervisor, Quality Assurance Manager, or Quality Director, often requiring experience, leadership skills, and knowledge of industry standards like ISO or GMP. Opportunities also exist in specialized areas such as validation, process improvement, and regulatory compliance, with certifications like Six Sigma or Lean Manufacturing enhancing career growth.

What is a QC stability specialist job description?

A QC stability specialist is responsible for testing and analyzing pharmaceutical or cosmetic products to ensure their stability over time. They develop stability protocols, monitor storage conditions, and interpret test results to confirm product quality and compliance with regulatory standards. Proficiency in laboratory techniques and knowledge of stability testing guidelines are essential for this role.

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.

What are the key skills and qualifications needed to thrive in the Qc Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What is a QC Stability job?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

What jobs make 10000 a month without a degree?

High-paying jobs that can reach $10,000 a month without a degree include roles such as sales managers, real estate brokers, commercial pilots, and certain skilled trades like electricians or plumbers with experience. Success in these fields often depends on experience, certifications, or licensing rather than formal education, and they may require strong interpersonal skills or technical training.
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Qc Stability jobs near you

QC Stability Manager

Abzena Inc.

San Diego, CA • On-site

Full-time

Posted 16 days ago

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.
The QC Stability Manager is responsible for leading and supporting GMP large-molecule stability testing across all phases of client programs within QC. This role provides strategic and operational leadership for the QC Stability function and manages a team of QC professionals. The position requires strong experience in QC laboratory operations, stability program management, and a deep understanding of cGMP/GDP requirements.
  • Leading analytical methods support activities related to stability testing, product control programs, and reference standard management.
  • Oversee daily operations of the QC Stability function in a biopharmaceutical manufacturing environment supporting multiple products and client programs.
  • Drive continuous improvement and operational efficiency across stability workflows, systems, and processes.
  • Ensure compliant operation and maintenance of stability-related infrastructure, documentation, equipment preventive maintenance, calibration, qualification, and training programs.

Responsibilities
People Leadership and Lab Management:
  • Provide leadership, mentorship, and development opportunities for QC staff and associates.
  • Ensure appropriate training of personnel in technical skills, cGMP compliance, data integrity, and safety requirements.
  • Communicate departmental goals, priorities, and performance expectations to direct reports.
  • Support facility teams in ensuring timely maintenance, calibration, and qualification of laboratory instruments and equipment.

Stability Program and Reference Standard Management:
  • Manage and oversee stability study design, protocol development, execution, and lifecycle management.
  • Coordinate stability protocol and report authoring in accordance with ICH guidelines, internal SOPs, and quality system requirements.
  • Oversee stability study setup, including sample management, material staging, and fraction tracking.
  • Track and monitor all active stability programs, including pull schedules, testing timelines, report completion, and Stability Summary Sheet issuance.
  • Maintain accurate and current stability inventory records.
  • Lead reference standard qualification, management, retesting, and lifecycle activities.
  • Monitor inventory, testing schedules, stability requirements, and timely issuance of associated certificates.
  • Provide training and oversight for laboratory personnel supporting reference standard activities.
  • Represent QC Stability in internal meetings, client meetings, audits, and cross-functional discussions related to stability and reference standards.
  • Ensure compliant analytical laboratory support and resource planning.
  • Author and/or review deviations, investigations, CAPAs, change controls, and risk assessments related to stability and reference standard programs.
  • Support or lead investigations involving OOS, OOT, non-conformances, and laboratory events.
  • Review analytical data packages, perform data trending, and provide troubleshooting support for complex laboratory issues.
  • Partner closely with Manufacturing, Analytical Development, Tech Transfer, Regulatory, and Quality Assurance teams.
  • Support strategic planning for new equipment, staff capacity planning, organizational structure, and resource requirements.
  • Recommend and justify additional equipment, staffing, promotions, or organizational changes as needed.
  • Occasional travel may be required between Abzena sites, including San Diego, California and Bristol, Pennsylvania.

Qualifications
  • Bachelor's degree or higher in Chemistry, Biology, or related Life Sciences discipline
  • Minimum 10 years of experience in QC GMP pharmaceutical or biotechnology laboratories within a cGMP-regulated environment
  • Minimum 5-6 years of people management experience in QC laboratory settings
  • Extensive knowledge of HPLC, SDS-PAGE, ELISA, Capillary Electrophoresis (CE), cIEF (Maurice platform), UV-Vis, cell-based potency assay, and compendial methods.
  • Knowledge of ICH, EP, USP, and FDA guidelines relating to method development, qualification/validation, and stability studies.

Core Competencies:
  • Excellent written, verbal, and interpersonal communication skills
  • Strong technical writing and documentation skills
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Strong organizational skills with ability to manage multiple priorities in a fast-paced, deadline-driven environment
  • Ability to proactively communicate risks, issues, and solutions to management
  • Strong troubleshooting, problem-solving, and decision-making skills
  • Detail-oriented with strong analytical mindset
  • Ability to work independently while collaborating effectively across teams
  • Experience supporting controlled document generation, review, and approval processes
  • Ability to draft and review Certificates of Analysis and reagent specification documents
  • Flexibility to work adjusted hours based on business needs

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 Jaws.
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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