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Quality Control Stability Coordinator Jobs (NOW HIRING)

Lonza

QC Specialist III-Stability

Portsmouth, NH · On-site

QC Specialist III-Stability Location: This position is based in our Portsmouth, NH office. The ... coordination, data tracking, and report generation. As a senior-level specialist, this position ...

Lonza

QC Specialist III-Stability

Portsmouth, NH

QC Specialist III-Stability Location: This position is based in our Portsmouth, NH office. The ... coordination, data tracking, and report generation. As a senior-level specialist, this position ...

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 ...

Moderna Therapeutics

$25.50 - $34.50/hr

As a QC Analyst, you will also support global GMP stability programs through a variety of operational and technical activities, including sample set downs, pulls, shipments, data trending and ...

ENFRA LLC

Quality Control Coordinator

Rayville, LA

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Montgomery, AL · On-site

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Rayville, LA · On-site

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Rayville, LA

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Rayville, LA

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Montgomery, AL

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Montgomery, AL

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

ENFRA LLC

Quality Control Coordinator

Montgomery, AL

$21.12 - $28.19/hr

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview The Quality Control Coordinator contributes to achieving consistent ...

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Quality Control Stability Coordinator information

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

As of Jun 8, 2026, the average hourly pay for quality control stability coordinator in the United States is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $26.20 per hour, depending on experience, location, and employer.

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

To thrive as a Quality Control Stability Coordinator, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by a bachelor’s degree and experience in quality control or laboratory environments. Familiarity with laboratory information management systems (LIMS), stability testing protocols, and regulatory guidelines such as GMP and ICH is typically required. Attention to detail, organizational skills, and effective communication are crucial soft skills for managing stability studies and collaborating with cross-functional teams. These competencies ensure accurate data management, regulatory compliance, and the reliability of product quality assessments.

What are Quality Control Stability Coordinators?

Quality Control Stability Coordinators are professionals responsible for managing and overseeing stability testing of products, typically in pharmaceutical or biotechnology industries. They ensure that products meet quality and regulatory standards by coordinating stability studies, tracking sample storage, and maintaining documentation. Their work helps determine how long products remain safe and effective under various environmental conditions. They also collaborate with different departments, such as quality assurance and manufacturing, to ensure compliance with regulatory guidelines.

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

AspectQuality Control Stability CoordinatorQuality Control Analyst
Primary FocusMonitoring product stability and ensuring consistency over timeTesting and analyzing products to ensure quality standards
CertificationsOften requires GMP, GLP, or industry-specific certificationsTypically requires GMP or relevant laboratory certifications
Work EnvironmentLaboratory and manufacturing settings, focusing on stability studiesLaboratory testing, data analysis, and quality assessment
Employer & Industry UsagePharmaceutical, biotech, and manufacturing industriesPharmaceutical, food, and consumer goods industries

The Quality Control Stability Coordinator primarily oversees product stability programs, ensuring products remain effective over time, while the Quality Control Analyst conducts testing and analysis to verify product quality. Both roles require similar certifications and work environments but focus on different aspects of quality assurance.

What are the main challenges a Quality Control Stability Coordinator faces when managing stability studies, and how can they effectively address them?

A Quality Control Stability Coordinator often encounters challenges such as coordinating multiple stability studies simultaneously, ensuring regulatory compliance, and maintaining accurate documentation. Managing timelines and responding to unexpected deviations in product stability can also be demanding. Effective communication with cross-functional teams, meticulous organization, and staying updated on regulatory guidelines help address these challenges. Utilizing robust data management systems and proactively identifying potential risks can further streamline the workflow and ensure the integrity of stability programs.
What are the most commonly searched types of Quality Control Stability jobs? The most popular types of Quality Control Stability jobs are:
Infographic showing various Quality Control Stability Coordinator job openings in the United States as of May 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $48,903 per year, or $23.5 per hour.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

$20.50 - $25.75/hr

Other

Posted 7 days ago

Job description

Description

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary:

Perform a variety of activities to administer the stability program and manage data generated in support of the company's quality program. 

Essential Responsibilities:

  • Comply with the requirements of stability standard operating procedure.
  • Data entry and usage of stability software.
  • Review stability program annually and recommend revision when necessary.
  • Provide stability summary to QC Director upon completion of study.
  • Assures that stability samples are disposed of according to GMP guidelines.
  • Will assist in preparing and maintaining batch records, certificate of analysis, maintain/control and file records of raw material specification and finished product specification.
  • Responsible for ensuring stability chambers and monitoring system are performing within set requirements. 
  • Employee uses professional skills and concepts to solve a variety of often complex situations. Able to make clear and concise decisions of vast importance in limited period of time. Must be able to perform multiple tasks in the proper sequence to effectively reach desired goals.

Requirements:

  • Minimum Associate's Degree, Bachelor's degree preferred in pharmacy, chemistry or related scientific field
  • 0-2 years' experience in Quality control laboratory.
  •  Knowledge of and ability to work with equipment, supplies, components and technical areas that are utilized in the    pharmaceutical industry.
  • Knowledge of FDA guidelines on Stability requirements is a plus;
  • Must be able to analyze data and work with a high degree of accuracy; 
  • Organized and able to perform duties in a timely manner; 
  • Must be flexible and able to handle multiple activities;
  • Must have excellent computer skills and verbal and written commutation skills.
  • Must be able to work in a team environment; team player.

Additional Preferred: 

  •  Experience in GMP quality control and/or pharmaceutical manufacturing facility; 
  • Pharmaceutical stability operations experience

Physical Conditions


Long periods of sitting, standing, walking, bending, stooping, reaching, and lifting. Will work around powders and other chemicals. Protective eyewear is necessary to wear in the laboratory or manufacturing.

Requirements

Preferred Knowledge & Skills:

  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.

Required Experience & Education:

  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
  • Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.

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