Stability Data Specialist

Eurofins View all jobs
Lexington, KY, United States
11 days ago
Apply on www.careerjet.com
Prepare application

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Experienced
Experience required
2 years minimum
Compensation
$64,480.0 - $72,800.0
Working hours
Regular working hours

Tech stack

Data Analysis Databases Data Integrity Analytic Functions

Job 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today!, This is a hybrid, non-laboratory role supporting Quality and Analytical functions. The successful candidate will collaborate with internal teams and external partners to ensure data integrity, regulatory compliance, and timely execution of deliverables. Key Responsibilities

  • Collaborate with departmental colleagues to complete assignments under supervision.
  • Review and interpret analytical data with client support; contribute to technical reports and regulatory documentation.
  • Evaluate QC testing data for small molecule and/or biologics methods from external vendor laboratories.
  • Enter GMP data into validated database systems accurately and efficiently.
  • Verify data and trending tables for inclusion in regulatory submissions.
  • Build and manage stability studies within validated systems, as applicable.
  • Ensure GMP data aligns with current specifications; generate Certificates of Analysis (COAs) when required.
  • Monitor and trend reference standards and analytical data.
  • Identify and escalate routine technical issues or vendor-related concerns.
  • Troubleshoot basic issues using available resources and guidance.
  • Travel between Lexington and Cambridge client sites as needed., Ability to move through building and to attend meetings across campus and off campus, sitting for long periods of time and repetitive motion tasks. Shift Days, Monday-Friday; 8:…
  • 14 days ago

Requirements

  • Bachelor’s degree in Chemistry, Biology, or a related field.
  • Minimum of 2 years of relevant industry experience.
  • Prior experience in Quality Control, Quality Assurance, or a GMP-regulated environment is required.
  • Experience in Analytical Development is preferred.
  • Familiarity with analytical methods for biologics or small molecule products is a plus.
  • Solid understanding of GMP principles and regulatory compliance.
  • Strong communication skills; able to document and report issues clearly and promptly.
  • Effective time management and multitasking abilities in a cross-functional team setting.
  • Must be authorized to work in the U.S. permanently without restriction or sponsorship

Benefits & conditions

Position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Lexington, MA are encouraged to apply. Occasional travel (approximately 1-2%) to the Cambridge, MA site may be required. Excellent full-time benefits include:

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $31.00-$35.00 per hour based on education and related experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website’s terms and privacy policy apply

About the company

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package., ## We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and i…

Apply for this position

This job is hosted externally. Click below to view the full posting and apply.

Apply on www.careerjet.com
Prepare application

Good distractions

Talks and stories from around this role — technically off-topic, practically not.

1:48 min

Automating exploratory data analysis within training pipelines

Dora Petrella · World Congress 2023

3:04 min

Database evolution and the funding behind vector databases

Erik Bamberg · LIVE

1:55 min

Maintaining software and data integrity during execution

Christian Wenz Christian Wenz · World Congress 2026 Europe

3:09 min

Balancing data science skillings alongside systems engineering rigor

Nico Schmidt · LIVE

4:47 min

Navigating data integrity and unpredictable generative AI outputs

Maish Saidel-Keesing Maish Saidel-Keesing · World Congress 2025

1:44 min

Background and career journey in regulated software systems

Martin Hynie · Coffee With Developers

Videos

See all

Related articles

See all