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Stability Study Pharmaceutical Jobs (NOW HIRING)

Genezen

Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

Conduct audits of stability studies and processes * Verify data for accuracy and compliance ... Regularly required to work around large machinery and typical utilities seen in pharmaceutical ...

Moderna Therapeutics

$25.50 - $34.50/hr

Execute stability study workflows within LIMS, including data entry, review, and approval * Support ... At least 5-7 years in Quality Control Laboratory of a Pharmaceutical Company * Demonstrated ...

Genezen

Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

Conduct audits of stability studies and processes * Verify data for accuracy and compliance ... 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

Conduct audits of stability studies and processes * Verify data for accuracy and compliance ... Regularly required to work around large machinery and typical utilities seen in pharmaceutical ...

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Stability Study Pharmaceutical information

What are some common challenges faced when conducting stability studies in the pharmaceutical industry?

One frequent challenge in stability studies is ensuring precise environmental control, as factors like temperature and humidity must be consistently maintained to produce reliable results. Additionally, coordinating sample collection and testing schedules requires strong organizational skills, since deviations can impact data integrity. Collaborating with cross-functional teams, such as quality assurance and manufacturing, is essential to address unexpected findings and ensure compliance with regulatory guidelines. Effective documentation and attention to detail are crucial throughout the process.

What is a Stability Study in the pharmaceutical industry?

A Stability Study in the pharmaceutical industry is a series of tests conducted on drug products to determine how long they maintain their intended quality, safety, and efficacy under various environmental conditions. These studies assess factors such as temperature, humidity, and light exposure to establish the shelf life and proper storage conditions for pharmaceuticals. Stability data is crucial for regulatory approval and ensures that medications remain effective throughout their intended use period.

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

To thrive as a Stability Study Pharmaceutical Specialist, you need a solid background in pharmaceutical sciences, analytical chemistry, and regulatory guidelines such as ICH, often supported by a relevant degree. Familiarity with laboratory instruments (HPLC, GC), LIMS, and good documentation practices, along with knowledge of regulatory compliance systems, is essential. Strong attention to detail, organizational skills, and effective communication help manage complex data and collaborate with cross-functional teams. These skills ensure accurate, compliant stability testing and reliable data critical for product safety and regulatory approval.

What is the difference between Stability Study Pharmaceutical vs Stability Study Chemist?

AspectStability Study PharmaceuticalStability Study Chemist
Required CredentialsBachelor's degree in Pharmacy, Chemistry, or related field; GMP trainingBachelor's or Master's in Chemistry or Pharmaceutical Sciences; GMP/GLP knowledge
Work EnvironmentPharmaceutical labs, quality control, R&D departmentsLaboratories focused on chemical stability testing, quality assurance
Employer & IndustryPharmaceutical companies, biotech firmsPharmaceutical, chemical manufacturing, research labs

Both roles involve stability testing, but the Stability Study Pharmaceutical typically focuses on drug products' shelf life and quality, while the Stability Study Chemist may work on broader chemical stability assessments across various products. The roles overlap in credentials and work environment, making them closely related in the pharmaceutical industry.

Infographic showing various Stability Study Pharmaceutical job openings in the United States as of May 2026, with employment types broken down into 65% Full Time, and 35% Part Time. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution.
Reference Standard Development Stability Management Inventory Manager

Reference Standard Development Stability Management Inventory Manager

Keywords Studios

Indianapolis, IN • On-site

$30/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

Job description

Location: Indianapolis, Indiana
Payrate: $30.00 an hour
The Reference Standard Development Stability Management Inventory Manager will manage the inventory of stability samples.
In addition, the individual will label, initiate stability studies, pull stability samples according to schedule, deliver or ship the samples to the corresponding receiver and reconcile inventory in the data management system.
The individual will also manage the inventory of GMP/clinical trial materials which can include shipping to multiple receivers.
Daily Responsabilities:
• Receive, store, label, forecast, submit, and deliver samples
• Support domestic and international shipping of material
• Conduct annual inventory of stored material
• Maintain documentation for stability studies in electronic system or logbook
• Support the client's work requests as needed
Requirements
Educational Requirements: An Associate degree in in chemistry or related field and/or significant pharmaceutical industry
experience or equivalent significant applicable experience.
Base Requirements:
• Excellent communication (oral and written) and attention to detail
• Strong computer and organizational skills, and experience with Microsoft Office Suite
• Ability to work independently and as part of a team, have self- motivation, adaptability, and a positive attitude
• Ability to learn new techniques, prioritize multiple tasks, keep accurate records, follow instructions, and comply with company policies
• No applicable drug allergies
• Must be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements
• Previous inventory experience is required.
• cGMP Lab or pharmaceutical science experience would be preferred.
Benefits
Keywords provides all its contingent workforce with:
Medical, dental and vision benefits
Paid time off (including sick and select holidays)
401(k) enrollment with 3% employer matching
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law
Role Information: EN
Studio: Keywords Studios
Location: Indianapolis, IN
Area of Work: Inventory
Service: DSM
Employment Type: Contractor
Working Pattern: Full Time
This Organization Participates in E-Verify
Keywords Studios is committed to fair and ethical hiring practices. We expect candidates to conduct themselves with honesty and to participate in all applications and interviews independently, presenting their own knowledge and experience. Candidates should refrain from using AI assistance or third-party tools or services that could influence, capture, or otherwise interfere with the authenticity of the assessment process
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About Keywords Studios

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Whatever the scale of your project, whatever the time frame, whatever your location: Keywords is here for you, bringing our network of 13,000+ people and 70+ studios together to deliver the unified solutions you need. We offer everything necessary to ensure your project achieves its full potential and that strategic opportunities are turned into long-term growth. The games industry is complex and fast-moving. Working with Keywords allows you to remain lean and agile, and to remain focused on creating the world’s most immersive playing experiences. Our network of studios brings best-in-class experience, expertise, technology and capacity across the full development, release and player-support lifecycle.

Industry

Arts, entertainment, and recreation

Company size

10,000+ Employees

Headquarters location

Burbank, CA, US

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