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Stability Study Pharmaceutical Jobs (NOW HIRING)

Eurofins

Stability Study Reviewer

Lancaster, PA · On-site

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 ...

Abzena Inc.

QC Stability Manager

San Diego, CA · On-site

Manage and oversee stability study design, protocol development, execution, and lifecycle ... Minimum 10 years of experience in QC GMP pharmaceutical or biotechnology laboratories within a cGMP ...

eTeam

Biological Researcher II

Chester, IL · On-site

... stability studies, and laboratory documentation within a biologics or pharmaceutical R&D environment. The ideal candidate should possess practical laboratory expertise, strong analytical and ...

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

Title: QC Stability Study Coordinator I Summary * With limited supervision, QC Stability Study ... Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical ...

Stryker

Associate Quality Manager, Stability

Cary, IL · On-site

$112K - $188K/yr

Provide strategic and operational oversight of stability study design, execution, monitoring, and ... Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards ...

TechData Service Company LLC

Be Seen First

Biological Researcher (SK9871)

West Chester, PA · On-site

$38 - $45/hr

Background in biologics, pharmaceutical sciences, biochemistry, chemical engineering, or related ... products. • Stability study sample preparation, pulls, and tracking • Analytical sample ...

Lonza

QC Specialist III-Stability

Portsmouth, NH · On-site

... pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination, tracking, and execution of stability studies * Demonstrated experience setting up stability ...

Lonza

QC Specialist III-Stability

Portsmouth, NH · On-site

... pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination, tracking, and execution of stability studies * Demonstrated experience setting up stability ...

Eurofins

Stability Protocol Writer

Lancaster, PA · On-site

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and ... Build stability studies based on client-provided protocols, ensuring all parameters are configured ...

Ageatia Global Solutions

QC Analyst

Vacaville, CA · On-site

$27.25 - $36.50/hr

Vacaville, CA-95688 Summary With limited supervision, QC Stability Study Coordinator, is ... Degrees are preferably in relevant scientific disciplines and experience is in the 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.
Stability Study Reviewer

Stability Study Reviewer

Eurofins

Lancaster, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 174 frontline employees who took The Breakroom Quiz

56th of 103 rated laboratories

Job description

Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
Eurofins Lancaster Laboratories is seeking a highly analytical and quality-driven Data Reviewer to ensure accuracy and compliance of all stability protocols and study builds prior to client release. This position plays a crucial role in safeguarding data integrity and ensuring that client expectations are consistently met.
This role includes a structured training progression: the individual will be fully trained as a Stability Protocol Reviewer prior to performing protocol and study review responsibilities. This ensures a deep understanding of both the technical content and system workflows that impact the quality of client deliverables.
Key Responsibilities
Training Phase - Protocol Writing & Study Building
  • Complete comprehensive training in protocol writing based on Eurofins-generated quotes.
  • Learn and practice building stability studies within the LIMS system following client-provided protocols.
  • Develop proficiency in interpreting client requirements, scientific documentation, and stability program workflows.

Primary Role - Data Review
  • Perform detailed, independent review of stability protocols and study builds to ensure accuracy, completeness, and alignment with client expectations.
  • Confirm that all protocol parameters (e.g., storage conditions, pull points, test plans) are correctly entered and consistent with both quotes and client-provided documents.
  • Verify compliance with GMP, internal SOPs, and industry guidelines.
  • Identify discrepancies, errors, or gaps and communicate effectively with Protocol Writers, Project Managers, and other stakeholders to resolve issues.
  • Ensure documentation is traceable, audit-ready, and maintained in accordance with data integrity principles (ALCOA+).
  • Support continuous improvements in review workflows, documentation standards, and system utilization.

Qualifications
Required
  • Bachelor's degree in a scientific discipline (Chemistry, Biology, Pharmaceutical Sciences, or related field) or equivalent industry experience.
  • Strong scientific comprehension and ability to interpret technical protocols, quotes, and study plans.
  • Exceptional attention to detail and commitment to data accuracy.
  • Strong communication skills with the ability to constructively collaborate and provide clear feedback.
  • Experience or familiarity with GMP, data integrity expectations, and regulated laboratory environments.
  • Ability to learn and work effectively within LIMS or similar informatics systems.

Additional Information
Position is full-time, Mon-Fri 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

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