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Qc Stability Manager Jobs (NOW HIRING)

... 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 ...

QC LCM / Stability Lead

Raleigh, NC · On-site

$98K - $138K/yr

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.

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

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 ...

Quality Control Manager The Quality Control Manager leads the Quality Control laboratory and ... This role oversees raw material, finished product, and stability testing, drives laboratory ...

Quality Control Manager The Quality Control Manager leads the Quality Control laboratory and ... This role oversees raw material, finished product, and stability testing, drives laboratory ...

The QC Manager will encourage and motivate associates to be successful and focused on Safety ... Supports the stability program including study management, protocol development & evaluation ...

The QC Manager will encourage and motivate associates to be successful and focused on Safety ... Supports the stability program including study management, protocol development & evaluation ...

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Qc Stability Manager information

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$30.5K

$81.3K

$129.5K

How much do qc stability manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for qc 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.

What is a QC Stability Manager?

QC Stability Managers are professionals responsible for overseeing the stability testing programs within pharmaceutical, biotechnology, or related industries. Their primary role is to ensure that products maintain their safety, efficacy, and quality throughout their shelf life by managing stability studies, analyzing data, and ensuring compliance with regulatory guidelines. They coordinate cross-functional teams, manage documentation, and ensure that stability protocols meet industry standards. QC Stability Managers also play a crucial role during audits and regulatory submissions by providing necessary data and reports. Their expertise helps companies maintain product quality and meet both internal and external regulatory requirements.

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

To thrive as a QC Stability Manager, you need a robust background in chemistry or pharmaceutical sciences, experience in stability testing, and a relevant degree such as a BS or MS. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (ICH, FDA), and analytical testing equipment like HPLC is essential. Strong organizational, leadership, and communication skills help manage teams, timelines, and cross-functional collaborations. These skills ensure the integrity of stability programs and compliance with regulatory standards, which are critical for product quality and approval.

What are the typical challenges faced by a QC Stability Manager in coordinating stability studies across multiple products?

QC Stability Managers often encounter challenges in managing multiple stability studies simultaneously, particularly when dealing with diverse product portfolios and strict regulatory timelines. Ensuring data integrity, timely sampling, and accurate documentation can be complex, especially when collaborating with cross-functional teams such as manufacturing, regulatory affairs, and quality assurance. Effective organization, proactive communication, and a strong understanding of regulatory requirements are essential for overcoming these challenges and maintaining compliance.

What is the difference between Qc Stability Manager vs Qc Analyst?

AspectQc Stability ManagerQc Analyst
CertificationsQuality certifications, stability testing trainingQuality certifications, laboratory training
Work EnvironmentLaboratory, quality control departmentsLaboratory, testing facilities
Employer & IndustryPharmaceutical, biotech, or chemical industriesPharmaceutical, biotech, or chemical industries
Primary FocusOverseeing stability programs, ensuring product shelf-lifePerforming stability testing, data analysis

The Qc Stability Manager focuses on managing stability programs and ensuring product shelf-life compliance, while the Qc Analyst conducts stability testing and analyzes data. Both roles require similar certifications and work in laboratory environments within the pharmaceutical or biotech industries, but their responsibilities differ in scope and leadership level.

What cities are hiring for Qc Stability Manager jobs?

Cities with the most Qc Stability Manager job openings:

What are the most commonly searched types of Qc Stability jobs?

The most popular types of Qc Stability jobs are:

What states have the most Qc Stability Manager jobs?

States with the most job openings for Qc Stability Manager jobs include:

What are popular job titles related to Qc Stability Manager jobs?

For Qc Stability Manager jobs, the most frequently searched job titles are:

Infographic showing various Qc Stability Manager job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Temporary - Senior Associate, QC Stability and Reference

Culver City, CA • On-site

$39/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

Company Overview
ImmunityBio is a vertically integrated commercial stage biotechnology company developing next-generation therapies that bolster the natural immune system to defeat cancers and infectious diseases. The Company's range of immunotherapy and cell therapy platforms, alone and together, act to drive and sustain an immune response with the goal of creating durable and safe protection against disease. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response. The Company is applying its science and platforms to treating cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies that we believe sharply reduce or eliminate the need for standard high-dose chemotherapy. These platforms and their associated product candidates are designed to be more effective, accessible, and easily administered than current standards of care in oncology and infectious diseases.
Why ImmunityBio?

ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.

Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.

Work with a collaborative team with the ability to work across different areas of the company.

Ability to join a growing company with professional development opportunities.


Position Summary

The IB Temporary - Senior Associate, QC Stability and Reference will perform activities to support the lmmunityBio stability and reference programs including activity scheduling and tracking, data trending, statistical analysis, investigations, and protocol and report drafting.

Essential Functions

  • Performs stability and reference coordination activities such as test forecasting, test scheduling, data entry, data trending, protocol and report drafting
  • Coordination and/or packing of stability and reference materials for shipment
  • Maintenance of controlled documents with stability reporting data
  • Maintain logs for stability and reference material, including inventory logs
  • Assist with updates for applicable modules of IND, BLA, or any other regulatory submission
  • Maintains equipment and completes maintenance records for stability chambers.
  • Support quality systems and documentation by completing change requests, updating SOPs and associated documents.
  • Performs other duties as assigned.

Education & Experience

  • Bachelor's degree in Biology or related field required
  • 2+ years' experience within a quality control testing setting in the Biotechnology industry required
  • Experience in GMP required

Knowledge, Skills, & Abilities

  • Excellent organization skills and attention to detail
  • Strong interpersonal and written and oral communication skills
  • Excellent problem solving skills
  • Ability to thrive in an efficient, highly interactive, goal-oriented team environment
  • Efficient Microsoft Word, PowerPoint and Excel skills
  • Knowledge of cGMP, FDA, ICH and USP regulations
  • Basic understanding of statistics

Working Environment / Physical Environment

  • Position is an on-site position
  • Exposure to onsite lab environment
  • Flexibility in working schedule may be required to complete work on off-hours in order to complete deadlines.
  • Ability to pack, ship, and receive stability and reference standards on site
  • Lift and carry materials weighing up to 20 pounds

The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$35.50 (entry-level qualifications) to $39.00 (highly experienced) per hour

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio uses artificial intelligence (AI) tools to assist with sourcing and identifying potential candidates for open positions. These tools help us reach qualified applicants and improve the efficiency of our recruitment outreach. No preference is given to applicants sourced or identified by AI tools.

Important: AI is not used to screen, evaluate, rank, assess, or make hiring decisions about applicants. All applications are reviewed by human recruiters and hiring managers. Hiring decisions are made solely by ImmunityBio personnel without automated decision-making.

We are committed to equal employment opportunity and ensure that all candidates are assessed based on their qualifications, skills, and experience through human review.


ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability Healthcare and Dependent Care Flexible Spending Accounts 401(k) Retirement Plan with Company Match 529 Education Savings Program Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks Paid Time Off (PTO) includes: 11 Holidays Exempt Employees are eligible for Unlimited PTO Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.


At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.