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Pharmaceutical Stability Jobs (NOW HIRING)

Stability Coordinator I

Garner, NC

$16.25 - $22/hr

The Stability Coordinator I is accountable for driving results in a fast-paced environment by ... Bachelor's degree in Pharmaceutical Sciences, Chemistry or equivalent preferred. * Prior cGMP ...

Stability Coordinator I

Garner, NC · On-site

$16.25 - $22/hr

Job Summary The Stability Coordinator I is accountable for driving results in a fast-paced ... Bachelor's degree in Pharmaceutical Sciences, Chemistry or equivalent preferred. * Prior cGMP ...

Stability Coordinator I

Garner, NC · On-site

$16.25 - $22/hr

Job Summary The Stability Coordinator I is accountable for driving results in a fast-paced ... Bachelor's degree in Pharmaceutical Sciences, Chemistry or equivalent preferred. * Prior cGMP ...

The position is highly hands-on and suited for a detail-oriented QC professional with strong stability program experience in a pharmaceutical or medical device GMP environment. This is a replacement ...

The position is highly hands-on and suited for a detail-oriented QC professional with strong stability program experience in a pharmaceutical or medical device GMP environment. This is a replacement ...

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and ... Learn and practice building stability studies within the LIMS system following client-provided ...

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Pharmaceutical Stability information

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How much do pharmaceutical stability jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for pharmaceutical stability in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a Pharmaceutical Stability job?

A Pharmaceutical Stability job involves evaluating the shelf-life and storage conditions of drug products to ensure their potency, safety, and efficacy over time. Professionals in this role conduct stability studies, analyze degradation patterns, and follow regulatory guidelines set by agencies like the FDA and ICH. They work closely with quality control, regulatory, and formulation teams to support product development and approval.

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

To thrive in Pharmaceutical Stability, you need a solid background in pharmaceutical sciences or chemistry, strong analytical abilities, and attention to detail, often underpinned by a bachelor’s or master’s degree in a relevant field. Familiarity with laboratory instrumentation (such as HPLC, GC, and dissolution testers), GMP regulations, and data management systems is essential. Strong organization, problem-solving skills, and effective teamwork and communication abilities set outstanding professionals apart. These skills ensure accurate stability testing, regulatory compliance, and successful collaboration within cross-functional teams in pharmaceutical development.

What are the typical daily responsibilities of someone working in Pharmaceutical Stability?

Professionals in Pharmaceutical Stability are primarily responsible for designing, executing, and documenting stability studies to ensure the quality and shelf-life of pharmaceutical products. Their daily tasks often involve preparing samples, conducting analytical tests using specialized lab equipment, recording data, and interpreting results in accordance with regulatory guidelines. They also collaborate regularly with formulation scientists, quality assurance teams, and regulatory affairs to support product development and submission activities. Attention to detail, adherence to standard operating procedures, and clear communication are essential parts of the job.

More about Pharmaceutical Stability jobs
What cities are hiring for Pharmaceutical Stability jobs? Cities with the most Pharmaceutical Stability job openings:
What are the most commonly searched types of Pharmaceutical Stability jobs? The most popular types of Pharmaceutical Stability jobs are:
What states have the most Pharmaceutical Stability jobs? States with the most job openings for Pharmaceutical Stability jobs include:
Infographic showing various Pharmaceutical Stability job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 50% Full Time, 29% Part Time, and 18% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

$20.50 - $25.75/hr

Full-time

Posted 9 days ago


Job description

Job Type
Full-time
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.