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 with 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 your work-life balance and a competitive benefits package.

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 of 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

We are seeking a detail-oriented and highly organized Nonclinical Regulatory Documentation Specialist to support quality control and submission readiness of nonclinical regulatory documents. This role will contribute to DMPK and Toxicology reporting, regulatory submission modules, and document lifecycle management in a fast-paced, compliance-driven environment.

Key Responsibilities

• Perform quality control (QC) review of nonclinical content for DMPK and Toxicology reports, as well as regulatory submission documents including Module 2 and Module 4.
• Provide editorial support, including document editing, formatting, and preparation of submission-ready Word and PDF files in accordance with internal style guides and global regulatory requirements.
• Support Veeva activities related to nonclinical regulatory document lifecycle management, including document routing, version control, and archival.
• Assist with literature reference-related activities, including reference retrieval, copyright clearance review, and upload to electronic document management systems.
• Independently identify and resolve issues, exercising sound judgment, effective communication, and flexibility within a dynamic, cross-functional environment.

• Bachelor’s degree in Life Sciences with 3–4+ years of relevant experience; regulatory submissions experience and/or professional certifications are a plus.
• Strong working knowledge of Good Laboratory Practices (GLP), FDA regulations, ICH guidelines, and the nonclinical drug development process.
• Proven ability to manage multiple projects and deadlines in a fast-paced environment.
• Exceptional attention to detail with strong written communication skills.
• Proficiency in Microsoft® Office tools, including Word, Excel, PowerPoint, and Visio.
• Experience with Veeva preferred; familiarity with other electronic document management or tracking systems is a plus
• Authorization to work in the United States indefinitely without restriction or sponsorship.

The position is Full Time, Monday through Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA, are encouraged to apply

What to Expect in the Hiring Process:

• 10-15 Minute Phone Interview with Regional Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader

What We Offer:

• 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
• Yearly goal-based bonus & eligibility for merit-based increases
• Compensation is between $90,000 - $100,000 annually, depending on education and experience 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.