Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
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Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA · On-site
$19 - $22/hr
Provide stability summary to QC Director upon completion of study. * Assures that stability samples ... Pharmaceutical stability operations experience Physical Conditions Long periods of sitting ...
The ability to interpret development, manufacturing, analytical, and stability data with scientific ... Partner with Pharmaceutical Development leads and cross-functional CMC teams to define authoring ...
The ability to interpret development, manufacturing, analytical, and stability data with scientific ... Partner with Pharmaceutical Development leads and cross-functional CMC teams to define authoring ...
Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing
Carlsbad, CA · On-site
... stability, specifications, control strategies) into clear, accurate, phase-appropriate regulatory ... Partner with Pharmaceutical Development leads and cross-functional CMC teams to define authoring ...
Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing
Carlsbad, CA · On-site
... stability, specifications, control strategies) into clear, accurate, phase-appropriate regulatory ... Partner with Pharmaceutical Development leads and cross-functional CMC teams to define authoring ...
Assistant Director / Associate Director, Pharmaceutical Development Regulatory Writing
Carlsbad, CA · On-site +1
Ionis Pharmaceuticals is seeking an experienced Pharmaceutical Development professional with a ... The ability to interpret development, manufacturing, analytical, and stability data with scientific ...
Assistant Director / Associate Director, Pharmaceutical Development Regulatory Writing
Carlsbad, CA · On-site +1
Ionis Pharmaceuticals is seeking an experienced Pharmaceutical Development professional with a ... The ability to interpret development, manufacturing, analytical, and stability data with scientific ...
Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing
Carlsbad, CA · On-site
Ionis Pharmaceuticals is seeking an experienced Pharmaceutical Development professional with a ... The ability to interpret development, manufacturing, analytical, and stability data with scientific ...
Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing
Carlsbad, CA · On-site
Ionis Pharmaceuticals is seeking an experienced Pharmaceutical Development professional with a ... The ability to interpret development, manufacturing, analytical, and stability data with scientific ...
Associate Director, Drug Product Development
Foster City, CA · Hybrid
$200K - $215K/yr
POSITION SUMMARY Mirum Pharmaceuticals is seeking an experienced Associate Director, Pharmaceutical ... of pharmaceutical analytical testing and demonstrated ability to interpret analytical, stability ...
Associate Director, Drug Product Development
Foster City, CA · Hybrid
$200K - $215K/yr
POSITION SUMMARY Mirum Pharmaceuticals is seeking an experienced Associate Director, Pharmaceutical ... of pharmaceutical analytical testing and demonstrated ability to interpret analytical, stability ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, KY · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, KY · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Director, CMC Stability
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end ... Degree in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering ...
Associate, Stability
Spokane, WA · On-site
$32.01 - $37.65/hr
Join a Leader in Pharmaceutical Manufacturing - And Build What's Next As Spokane's Largest ... Conduct special projects as directed by the QC Stability Supervisor and/or Manager, such as ...
Associate, Stability
Spokane, WA · On-site
$32.01 - $37.65/hr
Join a Leader in Pharmaceutical Manufacturing - And Build What's Next As Spokane's Largest ... Conduct special projects as directed by the QC Stability Supervisor and/or Manager, such as ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Associate Manager, Product Quality
Cary, IL · On-site
$112K - $188K/yr
Experience overseeing or supporting pharmaceutical stability programs. * Strong understanding of ... direct and indirect reports * Master of Arts (MA), Master of Science (MS), Certified Quality ...
Associate Director, Stability Management
Alameda, CA · On-site
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Associate Director, Stability Management
Alameda, CA · On-site
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Provide Quality Control review and analyze data from pharmaceutical stability studies to ensure ... Works under direct supervision and receives detailed instructions. * Develops competence by ...
Provide Quality Control review and analyze data from pharmaceutical stability studies to ensure ... Works under direct supervision and receives detailed instructions. * Develops competence by ...
Associate Director, Stability Management
Alameda, CA · On-site
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Associate Director, Stability Management
Alameda, CA · On-site
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Associate Director, Stability Management
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Associate Director, Stability Management
$172K - $244K/yr
SUMMARY/JOB PURPOSE: The Associate Director, Stability Management is responsible for the ... Experience in Pharmaceutical industry preferred. Knowledge/Skills: * Has extensive experience in ...
Director Pharmaceutical Stability information
What is the difference between Director Pharmaceutical Stability vs Pharmaceutical Stability Scientist?
| Aspect | Director Pharmaceutical Stability | Pharmaceutical Stability Scientist |
|---|---|---|
| Credentials | Advanced degree (PhD, MS) in pharmaceutical sciences or related field; extensive experience | Bachelor's or Master's degree in pharmaceutical sciences or related field; some experience |
| Work Environment | Leadership role overseeing teams and strategy in R&D or manufacturing | Hands-on research and testing within laboratories |
| Employer & Industry Usage | Pharmaceutical companies, biotech firms, contract research organizations |
The main difference is that the Director Pharmaceutical Stability leads and manages stability programs and teams, focusing on strategy and compliance, while the Pharmaceutical Stability Scientist conducts experiments and analyzes data to support stability assessments. Both roles are essential but differ in scope, responsibility, and seniority.
What are the most commonly searched types of Pharmaceutical Stability jobs?
The most popular types of Pharmaceutical Stability jobs are:
What are popular job titles related to Director Pharmaceutical Stability jobs?
For Director Pharmaceutical Stability jobs, the most frequently searched job titles are:

Lab Assistant (Stability Coordinator), Pharmaceutical Manufacturing
Chantilly, VA
$19 - $22/hr
Full-time
Re-posted 11 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
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.
We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.