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Stability Specialist I - job 1 of 2

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It 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 Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer 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

  • Understand and update LIMS appropriately for protocol and sample activities.
  • Manage inventory for incoming project samples; set up stability studies, label samples, and place into chambers.
  • Verify sample chamber placement, labeling, container counts, and LIMS entry
  • Pull samples from chambers at appropriate intervals; perform periodic chamber inventories
  • Maintain contents of stability chambers in an organized manner, monitor and change charts; clean inside of chambers
  • Follow all department procedures and SOPs; understand and apply GMP/GLP regulations to daily work; document data according to regulatory requirements
  • Attend department meetings
  • Independently evaluate and/or provide shipment paperwork, package samples for shipment as needed with additional training.
  • Effectively use word, tone, body language to share and receive information.
  • Accept and implement process change to support business goals.
  • Conducts all activities in a safe and efficient manner
  • Performs other duties as assigned

Qualifications

  • College degree in related field strongly preferred or High school diploma with 1+ year experience 

  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, Monday - Friday 6:00am - 2:00pm . 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 M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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Average salary estimate

$60000 / YEARLY (est.)
min
max
$50000K
$70000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Stability Specialist I, Eurofins

Are you looking to kickstart your career in the life sciences field? Join Eurofins Scientific as a Stability Specialist I in Lancaster, PA! In this exciting role, you’ll be part of a dynamic team dedicated to ensuring the safety and quality of critical products like food, water, and pharmaceuticals. As a Stability Specialist I, your day-to-day will involve managing project samples, setting up stability studies, and maintaining the organization of our precision chambers. But don't worry, you won't do this alone! You'll get to collaborate with colleagues while following standard operating procedures and adhering to Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) regulations. This role also includes the critical task of updating the Laboratory Information Management System (LIMS), ensuring that data is accurately documented according to regulatory requirements. It's a fantastic opportunity for someone with a college degree in a related field or a high school diploma paired with some relevant experience. As part of Eurofins, you’ll have access to excellent benefits, including comprehensive medical options, a 401(k) plan with company matching, and generous paid vacation. If you're an enthusiastic team player ready to help make the world healthier and safer, we can't wait to meet you!

Frequently Asked Questions (FAQs) for Stability Specialist I Role at Eurofins
What are the primary responsibilities of a Stability Specialist I at Eurofins Scientific?

As a Stability Specialist I at Eurofins Scientific, your primary responsibilities will include managing project samples, setting up stability studies, updating the Laboratory Information Management System (LIMS), and ensuring the organization and cleanliness of stability chambers. You will perform essential tasks such as sample labeling, chamber inventories, and documentation according to GMP and GLP standards.

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What qualifications are needed for the Stability Specialist I role at Eurofins Scientific?

For the Stability Specialist I position at Eurofins Scientific, a college degree in a related field is strongly preferred, although candidates with a high school diploma and at least one year of relevant experience will also be considered. It's essential that candidates are authorized to work in the United States indefinitely without restrictions.

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How does Eurofins Scientific support employees in the Stability Specialist I position?

Eurofins Scientific provides robust support for their Stability Specialists I through comprehensive training, a structured onboarding process, and clear documentation protocols. Employees will have access to mentoring and will participate in department meetings, which fosters continuous professional development within the organization.

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What benefits can I expect as a Stability Specialist I at Eurofins Scientific?

As a Stability Specialist I at Eurofins Scientific, you can expect a competitive benefits package that includes excellent medical, dental, and vision coverage, life and disability insurance, a 401(k) plan with company matching, as well as paid vacation and holidays—promoting a healthy work-life balance.

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What does a typical work schedule look like for a Stability Specialist I at Eurofins Scientific?

The typical work schedule for a Stability Specialist I at Eurofins Scientific is full-time, Monday through Friday, from 6:00 AM to 2:00 PM. This consistent schedule allows employees to maintain a balanced lifestyle while contributing to the critical work of ensuring product safety and quality.

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Common Interview Questions for Stability Specialist I
What experience do you have that is relevant to the Stability Specialist I role?

When responding, mention any laboratory experience you have, especially relating to handling samples, using LIMS, or adhering to GMP and GLP guidelines. Highlight how your background prepares you for the challenges of the role at Eurofins Scientific.

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How do you prioritize your tasks when managing samples and stability studies?

Discuss your approach to prioritization, such as creating a daily task list, using organizational skills, or references to software tools. Emphasize how maintaining accuracy and compliance is your top priority.

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Can you describe a time when you had to adapt to process changes?

Provide an example that showcases your flexibility in adapting to new processes or procedures. Highlight your success in implementing the change effectively while still meeting quality standards.

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Describe your experience with documentation and regulatory compliance.

Explain your familiarity with creating accurate reports and following specific guidelines, particularly in scientific or laboratory settings. Discuss any relevant training or certifications you have that support your knowledge in this area.

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How do you ensure accuracy when updating LIMS?

Discuss the steps you take to ensure accuracy, such as double-checking data entries, conducting periodic audits of the information, or leveraging software features that minimize errors.

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What strategies do you use to maintain organization in the lab?

Share your methods for keeping the workspace organized, such as labeling, creating inventory systems, and regularly cleaning and maintaining lab equipment to enhance productivity.

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How do you handle tight deadlines in a laboratory environment?

Explain your approach to managing deadlines by emphasizing time management skills, prioritization of tasks, and seeking assistance from team members when needed to meet project requirements while ensuring quality.

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What safety protocols do you consider essential for a Stability Specialist?

Talk about your understanding of laboratory safety protocols, such as proper handling of samples, wearing personal protective equipment (PPE), and knowledge of standard operating procedures that ensure a safe working environment.

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In your opinion, what is the most important aspect of quality control in stability studies?

Discuss how quality control affects the integrity of the study results. Mention the importance of adhering to protocols and maintaining consistent monitoring to meet regulatory expectations.

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Why do you want to work at Eurofins Scientific as a Stability Specialist I?

Personalize your response by aligning your career goals with Eurofins' mission. You might mention their dedication to quality and safety and how it resonates with your professional aspirations in the life sciences field.

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FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
March 20, 2025

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