ZipRecruiter

Log In

1

Quality Control Stability Jobs (NOW HIRING)

Kelly Services

QC LCM / Stability Lead

Raleigh, NC

$98K - $138K/yr

QC LCM / Stability Lead Location: Raleigh, NC Salary: $98,000-$138,000/year Schedule: Fully onsite, Monday-Friday, normal business hours Position Summary The QC LCM / Stability Lead provides ...

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 ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Ardena

Scientist - Quality Control (QC)

Somerset, NJ · On-site

Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time ... Perform analytical testing of raw materials, in-process materials, finished products, and stability ...

Novartis

Senior Expert Stability

East Hanover, NJ · On-site

$118K/yr

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

20BLOC

QUALITY CONTROL (QC) LEAD

Thousand Oaks, CA · On-site

$90K - $110K/yr

How you will add value to 20BLOC The Quality Control (QC) Lead manages our QC group, leads the ... stability using equipment and instruments supporting biotherapeutics. Transfer developed and ...

20BLOC

QUALITY CONTROL (QC) LEAD

Thousand Oaks, CA · On-site

$90K - $110K/yr

How you will add value to 20BLOC The Quality Control (QC) Lead manages our QC group, leads the ... stability using equipment and instruments supporting biotherapeutics. Transfer developed and ...

previous pagenext page

Showing results 21-40

All JobsManufacturing JobsProduct Manufacturing JobsQuality Control Inspector JobsQuality Control Stability Jobs

Quality Control Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do quality control stability jobs pay per year?

As of Sep 7, 2026, the average yearly pay for quality control 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 is a quality control stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

What are some common challenges faced in a quality control stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a quality control stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

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

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.
More about Quality Control Stability jobs

What cities are hiring for Quality Control Stability jobs?

Cities with the most Quality Control Stability job openings:

What are the most commonly searched types of Quality Control Stability jobs?

The most popular types of Quality Control Stability jobs are:

What states have the most Quality Control Stability jobs?

States with the most job openings for Quality Control Stability jobs include:

What job categories do people searching Quality Control Stability jobs look for?

The top searched job categories for Quality Control Stability jobs are:

Quality Control Stability jobs near you

QC Microbiology & Stability Scientist

Harrow, Inc.

Ledgewood, NJ • On-site

$25.50 - $33.75/hr

Full-time

Re-posted 10 days ago

Job description

Before reading the job post, we encourage you to watch this video about our company. It gives you an inside look at how we started, the team and culture that made us successful, and where we're going. It's easy to read a job post and apply, but people often wonder about the culture and whether they would fit in. If you want to call Harrow your home and genuinely want to be part of a family and something big, then we encourage you to click this link and get to know us.
Who is Harrow?
Harrow (Nasdaq: HROW) is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company - where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow's values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable medicines, and (3) our track record of having never turned down an ophthalmologist doing mission work around the world - providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need. We encourage you to learn more about Harrow and its unique culture to see if you're the right person to help contribute as we build a truly exceptional company, one we are all so proud of!
Harrow's ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including:
  • An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZTM, and OPUVIZTM
  • A broad Dry Eye Disease product line, led by VEVYE® and bolstered by well-known adjacent ocular surface disease products such as FLAREX® and FRESHKOTE®
  • A peri-operative Surgical product line, led by TRIESENCE®, and BYQLOVITM
  • A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO®, NATACYN®, and VERKAZIA®
  • A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01

Job Summary
This position is responsible for performing microbiological testing, data review, and managing stability program activities in support of product quality, regulatory compliance, and GMP manufacturing. Assist with the QC samples, including raw materials, stability, and finished drug products. This role supports environmental monitoring, microbial testing, stability studies, and data review while ensuring adherence to regulatory requirements and internal quality standards.
Core Responsibilities
  • Ensure compliance with GMP, FDA, and ICH guidelines.
  • Prepare and maintain laboratory documentation, including SOPs, protocols, and reports.
  • Participate in internal audits, regulatory inspections, and quality improvement initiatives.
  • Support deviation investigations, CAPAs, and change control activities.
  • Handles all QC samples, including raw materials, finished drug products, and stability samples, for submission to appropriate analytical testing laboratories, including making out submission paperwork or entry forms and shipping the samples to outside laboratories
  • Follows up with laboratories on past due test results
  • Other duties will be assigned as required to support QC and Quality

QC Microbiology
  • Perform routine and non-routine microbiological testing, including:
    • Environmental monitoring (air, surface, personnel)
    • Bioburden testing
    • Microbial limits testing
    • Endotoxin testing
    • Sterility testing (as applicable)
  • Conduct microbial identification using approved methods.
  • Perform media preparation, growth promotion testing, and equipment qualification.
  • Review microbiological data and ensure accuracy, completeness, and compliance with GMP requirements.
  • Investigate out-of-specification (OOS), out-of-trend (OOT), and environmental monitoring excursions.
  • Support method validation, method transfers, and laboratory investigations.

Stability Program Management
  • Coordinate and manage stability studies in accordance with ICH and regulatory guidelines.
  • Prepare and maintain stability protocols, schedules, and reports.
  • Manage stability sample inventory, storage, and testing timelines.
  • Track stability time points and ensure timely testing and documentation.
  • Review and analyze stability data to support product shelf-life and regulatory submissions.
  • Maintain stability chambers and monitor environmental conditions.
  • Enters all stability sample information and data into the stability management software
  • Provides stability data and analysis for Annual Product Quality Review (APQR) reports.

Qualifications & Requirements
  • Bachelor's Degree in scientific discipline.
  • 5 years of pharmaceutical laboratory environment experience; or equivalent combination of education and experience.
  • Must be detail oriented
  • Must be well organized
  • Must have the ability to work on multiple different tasks within a workday
  • Must have a positive teamwork attitude
  • Excellent interpersonal, oral, and written communication skills
  • Maintains confidentiality of sensitive information
  • Ability to meet attendance standards. All full-time employees are required to work a minimum of 40 hours in a week. Sometimes it may be necessary to work additional hours to accomplish the required tasks to meet deadlines

Position Type
  • On-Site

Travel
  • None
Harrow logo

About Harrow

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Nashville, TN, US

Year founded

1998

View All Harrow Jobs

Apply