Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Quick apply
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Perform a variety of activities to administer the stability program and manage data generated in ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Stability Coordinator/Manager
San Diego, CA · On-site
$100K - $125K/yr
The Stability Coordinator / Manager is responsible for planning, coordinating, and managing drug ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Stability Coordinator/Manager
San Diego, CA · On-site
$100K - $125K/yr
The Stability Coordinator / Manager is responsible for planning, coordinating, and managing drug ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Stability Coordinator/Manager
San Diego, CA · On-site
Description The Stability Coordinator / Manager is responsible for planning, coordinating, and ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Stability Coordinator/Manager
San Diego, CA · On-site
Description The Stability Coordinator / Manager is responsible for planning, coordinating, and ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Stability Coordinator/Manager
San Diego, CA · On-site
The Stability Coordinator / Manager is responsible for planning, coordinating, and managing drug ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Quick apply
Stability Coordinator/Manager
San Diego, CA · On-site
The Stability Coordinator / Manager is responsible for planning, coordinating, and managing drug ... S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related discipline with 4+ years of ...
Stability Coordinator
Winston Salem, NC · On-site
Experience with Agile PLM (Product Lifecycle Management) / PQM (Product Quality Management) * Previous work history involving stability studies at a food, supplement, pharmaceutical, or cosmetic ...
Stability Coordinator
Winston Salem, NC · On-site
Experience with Agile PLM (Product Lifecycle Management) / PQM (Product Quality Management) * Previous work history involving stability studies at a food, supplement, pharmaceutical, or cosmetic ...
As a result of the company's expansion of its Pharmaceutical Development and Manufacturing department, our client is seeking a talented and motivated Director of Stability Management, Analytical ...
As a result of the company's expansion of its Pharmaceutical Development and Manufacturing department, our client is seeking a talented and motivated Director of Stability Management, Analytical ...
Stability Coordinator
Winston Salem, NC · On-site
Experience with Agile PLM (Product Lifecycle Management) / PQM (Product Quality Management) * Previous work history involving stability studies at a food, supplement, pharmaceutical, or cosmetic ...
Stability Coordinator
Winston Salem, NC · On-site
Experience with Agile PLM (Product Lifecycle Management) / PQM (Product Quality Management) * Previous work history involving stability studies at a food, supplement, pharmaceutical, or cosmetic ...
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years. * 6+ years in stability management or relevant ...
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years. * 6+ years in stability management or relevant ...
QC Stability Coordinator
Tonawanda, NY · On-site
$26/hr
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
Quick apply
QC Stability Coordinator
Tonawanda, NY · On-site
$26/hr
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
QC Stability Coordinator
Tonawanda, NY · On-site
$26/hr
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
QC Stability Coordinator
Tonawanda, NY · On-site
$26/hr
The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals ... The Stability Coordinator is expected to manage multiple concurrent projects, contribute to ...
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Quick apply
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Quick apply
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Quick apply
Laboratory Product Support
Clayton, NC · On-site
$28 - $30/hr
... for pharmaceutical products. Responsibilities: * Manage stability sample inventory, documentation, labeling, storage, and delivery for active stability studies. * Coordinate sample acquisition ...
Senior Manager, Stability Management, Analytical Development and Quality
Redwood City, CA · On-site
$164K - $205K/yr
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years. * 6+ years in stability management or relevant ...
Senior Manager, Stability Management, Analytical Development and Quality
Redwood City, CA · On-site
$164K - $205K/yr
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 8+ years of industry experience; or MS with 10+ years, or BS with 12+ years. * 6+ years in stability management or relevant ...
Director, Stability Management, Analytical Development and Quality Control
Redwood City, CA · Hybrid
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 12+ years of industry experience; or MS with 15+ years, or BS with 18+ years. * 10+ years in stability management or relevant ...
Director, Stability Management, Analytical Development and Quality Control
Redwood City, CA · Hybrid
PhD in Chemistry, Pharmaceutical Sciences, or related discipline with 12+ years of industry experience; or MS with 15+ years, or BS with 18+ years. * 10+ years in stability management or relevant ...
Contract: Manager, CMC Stability Management and Analysis
Bothell, WA · On-site
$99K - $133K/yr
Manager, CMC Stability Management and Analysis to oversee execution of outsourced stability ... Bachelor's or advanced degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology ...
Contract: Manager, CMC Stability Management and Analysis
Bothell, WA · On-site
$99K - $133K/yr
Manager, CMC Stability Management and Analysis to oversee execution of outsourced stability ... Bachelor's or advanced degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Manage stability programs in accordance with ICH Q1A(R2) and Hikma procedures. * Maintain stability ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or related discipline ...
Stability Administrator
Bedford, OH · On-site
$44K - $74K/yr
Manage stability programs in accordance with ICH Q1A(R2) and Hikma procedures. * Maintain stability ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or related discipline ...
Pharmaceutical Stability Manager information
See salary details
$24.5K - $32.8K
9% of jobs
$32.8K - $41.1K
15% of jobs
$41.8K is the 25th percentile. Wages below this are outliers.
$41.1K - $49.5K
17% of jobs
The median wage is $52.3K / yr.
$49.5K - $57.8K
27% of jobs
$62.9K is the 75th percentile. Wages above this are outliers.
$57.8K - $66.1K
12% of jobs
$66.1K - $74.4K
8% of jobs
$74.4K - $82.7K
4% of jobs
$82.7K - $91K
3% of jobs
$91K - $99.4K
2% of jobs
$99.4K - $107.7K
2% of jobs
$107.7K - $116K
1% of jobs
$24.5K
$59.5K
$116K
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What are some common challenges faced by a pharmaceutical stability manager when coordinating cross-functional teams during stability studies?
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The top searched job categories for Pharmaceutical Stability Manager jobs are:

Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA
$19 - $22/hr
Full-time
Re-posted 24 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.Â
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.Â
- 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;Â
- Organized and able to perform duties in a timely manner;Â
- 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:Â
- Â Experience in GMP quality control and/or pharmaceutical manufacturing facility;Â
- 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
 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;Â
- Organized and able to perform duties in a timely manner;Â
- 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:Â
- Â Experience in GMP quality control and/or pharmaceutical manufacturing facility;Â
- 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.Â
We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.