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Pharmaceutical Stability Manager 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 ... Minimum 10 years of experience in QC GMP pharmaceutical or biotechnology laboratories within a 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 ... Regularly required to work around large machinery and typical utilities seen in pharmaceutical ...

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 ... Regularly required to work around large machinery and typical utilities seen in pharmaceutical ...

MedPharm

Metrologist

Durham, NC · On-site

... pharmaceutical laboratory and manufacturing equipment. * Maintains all logs and required ... Work closely with Validations and Stability Manager, Lab Operations, Manufacturing and Quality to ...

MedPharm

Metrologist

Durham, NC · On-site

... pharmaceutical laboratory and manufacturing equipment. * Maintains all logs and required ... Work closely with Validations and Stability Manager, Lab Operations, Manufacturing and Quality to ...

MedPharm

Metrologist

Durham, NC · On-site

... pharmaceutical laboratory and manufacturing equipment. * Maintains all logs and required ... Work closely with Validations and Stability Manager, Lab Operations, Manufacturing and Quality to ...

MedPharm

Metrologist

Durham, NC · On-site

... pharmaceutical laboratory and manufacturing equipment. * Maintains all logs and required ... Work closely with Validations and Stability Manager, Lab Operations, Manufacturing and Quality to ...

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Pharmaceutical Stability Manager information

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$24.5K

$59.5K

$116K

How much do pharmaceutical stability manager jobs pay per year?

As of Jun 9, 2026, the average yearly pay for pharmaceutical stability manager in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a Pharmaceutical Stability Manager when coordinating cross-functional teams during stability studies?

Pharmaceutical Stability Managers often encounter challenges in aligning timelines and expectations among cross-functional teams, such as quality assurance, analytical development, and manufacturing. Effective communication is essential to ensure that sample collection, testing, and documentation happen according to regulatory guidelines. Additionally, managing unexpected results or delays requires strong problem-solving skills and flexibility. Building collaborative relationships and maintaining clear documentation are key to overcoming these challenges and ensuring the success of stability programs.

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

To thrive as a Pharmaceutical Stability Manager, you need a strong background in chemistry or pharmaceutical sciences, experience with stability testing, and a relevant degree (often a BS or MS). Expertise in analytical instruments (such as HPLC and GC), familiarity with LIMS, and knowledge of ICH guidelines or regulatory compliance are typically required. Strong project management, attention to detail, and effective communication skills help in coordinating teams and ensuring data integrity. These skills are crucial for maintaining product quality, ensuring regulatory compliance, and driving successful stability programs.

What are Pharmaceutical Stability Managers?

Pharmaceutical Stability Managers are professionals responsible for overseeing stability studies that ensure the safety, efficacy, and quality of pharmaceutical products throughout their shelf life. They design, implement, and monitor stability testing programs according to regulatory guidelines, analyze results, and prepare documentation for regulatory submissions. Their role is crucial in determining storage conditions and expiration dates for medications, ensuring compliance with industry standards and regulations.
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Pharmaceutical Stability Manager jobs near you
Infographic showing various Pharmaceutical Stability Manager job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Nights. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $59,525 per year, or $28.6 per hour.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

$20.50 - $25.75/hr

Full-time

Posted 8 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.

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