Senior Toxicologist

Eurofins BioPharma Product Testing North America; Lancaster (Lancaster County); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Comprehensive medical coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins BioPharma Product Testing North America is looking for a Senior Toxicologist based in Lancaster County, United States. The role involves preparing toxicological risk assessments, conducting data reviews, and leading project teams. Candidates should have an advanced degree in Toxicology and significant experience in related tasks. Excellent communication and leadership skills are essential. The position offers full-time benefits including health insurance and a 401(k) plan.

Qualifications

• PhD in Toxicology or related field with 2-5 years of relevant experience.
• Strong expertise in ISO 10993 requirements and risk assessment principles.
• Authorization to work in the United States indefinitely.

Responsibilities

• Independently prepare toxicological risk assessments on medical devices.
• Conduct gap analyses and independent data reviews.
• Lead and coordinate projects demonstrating autonomy and accountability.

Skills

Toxicology expertise

Leadership skills

Communication skills

Organizational skills

Education

PhD in Toxicology or related field

MS in scientific discipline with 7 years experience

BS in scientific discipline with 10 years experience

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.

Job Description

As a Senior Toxicologist your responsibilities will include, but are not limited to, the following:

• Independently prepare toxicological risk assessments (TRAs) on medical device extractable and leachable compounds in accordance with ISO 10993-17:2023
• Independently prepare toxicological risk assessments on container closure and single-use system extractable and leachable compounds
• Demonstrate expertise in developing scientifically justified read‑across approaches and interpreting QSAR model outputs
• Conduct gap analyses and independent data reviews
• Develop biological evaluation plans (BEPs) and reports (BERs)
• Perform peer review of toxicological reports to ensure scientific accuracy, quality, and regulatory compliance
• Independently prepare and submit responses to regulatory deficiencies, maintaining high scientific and regulatory standards
• Assess and interpret client requirements to provide strategic input on new projects
• Pursue and maintain relevant professional memberships to support ongoing professional development
• Display leadership and initiative (e.g., process improvements, development of meeting abstracts/presentations)
• Remain abreast of advances in the field (e.g., participation in AAMI working groups)
• Proactively identify and implement best practices to drive continuous improvement
• Lead and coordinate projects of moderate scope, demonstrating autonomy and accountability

Qualifications

Your Basic Minimum Qualifications:

• PhD in Toxicology or related field with 2‑5 years of relevant experience
• MS in scientific discipline with a minimum of 7 years of experience in toxicology or related fieldBS in scientific discipline with minimum of 10 years of experience in toxicology or related field
• Demonstrated proficiency in ISO 10993 requirements, with comprehensive knowledge of applicable industry and regulatory standards
• Strong expertise in toxicology, including systemic, carcinogenic, and reproductive/developmental toxicity, with comprehensive knowledge of risk assessment principles
• Authorization to work in the United States indefinitely without restriction or sponsorship

Ideal Candidate

As the ideal candidate you would possess:

• 3 years of experience in performing biological evaluations/reports and TRAs in accordance with ISO 10993-17:2023
• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self‑motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Strong leadership, initiative, and team‑building skills

Additional Information

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

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