Principal Toxicologist Position Available In Lancaster, Pennsylvania

Company DescriptionEurofins 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.

In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job DescriptionJob DescriptionAs a Toxicologist your responsibilities will include, but are not limited to, the following:

Prepare hazard identification and toxicology risk / safety assessments for impurities, excipients, leachables, extractables, etc.

Conduct SAR and QSAR modelling of compoundsReview, interpret, and position data (study reports, literature, safety data)Conduct technical dossier gap analysis and independent data reviewsValidity review of performed studiesRemain abreast of advances in the fieldActively participate in US working groups for standards development (e.g., AAMI)Provide technical support and guidance on client callsServe as a thought leader and mentor to junior members of the team

Essential Duties and Responsibilities:

Applies GMP/GLP in all areas of responsibility, as appropriateMeets all quality and productivity metrics and demonstrates strong teamwork and collaborationPerforms laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precisionPerform/review preparations of reagents, samples, and standards according to procedures.

Perform routine, non-routine and complex analyses; instrumental analyses; including calibration and troubleshooting/repair of instruments independentlyMake technical decisions without consulting managementGuide and mentor junior staff to successfully complete projects and grow technical knowledgeDo independent research into regulatory trends and technical advancesBe a technical resource for internal problems throughout ELLIProvide support for corporate initiatives through BPT networkProvide coverage for management when neededDocument testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements – striving to minimize errorsUnderstand and perform calculations as required by test methodsUnderstand and utilize computers for information access, calculations, and report preparationRead and understand analytical procedures (compendial and client supplied) and internal SOP’sAssist with onboarding new instrumentation, including performing/reviewing

IQ/OQ/PQ

data or qualificationsProvide consultation for clientsDemonstrate technical writing skills and complete investigations independentlyDemonstrate leadership qualities including;Effective communicationDisplay confidenceDemonstrate motivation and take initiativeFollow through on assignmentsProcess/review data, generate/review reports, and evaluate dataCommunicate effectively, both orally and in writingSuggest and implement lab improvements or modify existing processes to maximize quality and productivity; support and drive LEAN initiativesSupport or identify speaking or publishing opportunities and assist with driving to publication or presentationCommitment to occasional overtime as workload requires

QualificationsMinimum Qualifications:

Bachelors Degree in Toxicology or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)Authorization to work in the US without immediate OR future sponsorship Minimum of 10 years’ experience performing biological evaluations of medical devices per

ISO10993

(i.e., authoring biological evaluation plans (BEPs), biological evaluation reports (BERs), and toxicological risk assessments (TRAs) Strong understanding of the full scope of

ISO 10993

as well as other relevant industry and regulatory standardsGood dexterity; positive attitude; solution driven; good work habits (organized, efficient, careful, safety-conscious, accurate); attention to detail; sound scientific logic; good oral and written communication skills; understanding of multiple instrumentation platforms and/or instrumental theory; client service focused; demonstration of organizational skills; ability to independently work on complex projects; ability to multitask; technical writing skills

Additional Preferences:

Certification as a Diplomate of the American Board of Toxicology (DABT) Involvement and leadership in relevant international standards committees (e.g., ISO, AAMI, etc.) 10 years experience in performing biological evaluations of medical devices on the basis of

ISO10993-17.

 Advanced degree in toxicology or related degree concentration Familiarity with a broad range of medical device applicationsStrong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivation, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesStrong leadership, initiative, and teambuilding skillsAdditional InformationWorking schedule will be Full-Time, First Shift, 8am-5pm M-F. Overtime may be required when necessary. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. This position is NOT remote. What we

Offer:

Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.