Scientist, Toxicology

Job Description The Nonclinical Drug Safety (NDS) group at the West Point, PA site is seeking an individual with strong technical and communication skills to join the Central Pharmacy laboratory within the Toxicological Sciences group. The Central Pharmacy is responsible for preparing vehicle and test article dosing formulations to support GLP‑compliant and exploratory nonclinical studies. Additional study support activities include maintaining documentation in an electronic document management system, coordinating collection of samples of dosing formulations for analysis, authoring the test and control article information section of study reports, and receiving and shipping materials to support internal and contract research organization studies. Scientists also maintain the pharmacy’s test and control article, chemical GLP reserve sample, and controlled substance inventories. The position is a 5 day/week schedule, including coverage of weekends and holidays on a rotational basis. Primary Responsibilities Follow Standard Operating Procedures (SOPs), GLP requirements, and safety requirements. Perform tasks to execute assigned nonclinical studies. Collaborate with study stakeholders. Review and verify the test and control article section of the study protocol. Create dosing formulation preparation instructions to support various routes of administration including oral, intravenous, intramuscular, and subcutaneous. Perform accurate weighing of test and control articles. Prepare suspension and/or solution dose formulations daily or in bulk based on stability information using weight‑to‑weight or weight‑to‑volume techniques. Utilize standard formulation equipment such as a stir plate, water bath sonicator, pH meter, and homogenizer. Compile test and control article documentation needed to support the study. Author the test and control article section(s) of study reports. Apply sound basic laboratory skills that include observing, recording, and assessing data. Maintain accurate and highly detailed laboratory records. Work with several data acquisition computer systems/applications. Maintain laboratory functionality and inspection readiness by accurate maintenance of the CP inventory including compounds, lab supplies, and equipment. Other Responsibilities Contribute to Central Pharmacy and cross‑functional projects. Train and work cross‑functionally in other areas within NDS and Preclinical Development. Educational Minimum Requirements BS/BA in Chemistry, Biology, or a related discipline with some relevant laboratory experience. Required Experience and Skills 1+ year of relevant laboratory experience. Knowledge of the chemistry of solutions and suspensions, including concentration, weight‑ and volume measurements, density, and other aspects of weight‑to‑volume/weight preparations. Strong listening, communication (verbal and written), and collaboration skills. Ability to problem‑solve in a fast‑paced environment and deliver results to meet timelines. Ability to work independently on assigned nonclinical studies and projects as well as being able to work in teams both within Central Pharmacy and cross‑departmentally, while adhering to the highest standards of trustworthy and ethical behavior in all interactions. Familiarity with recording and assessing laboratory data. Working knowledge of Microsoft Office suite, predominately Outlook/Teams, Word, Excel, and PowerPoint. Preferred Experience and Skills Experience in the pharmaceutical industry or biotech, or similar. Regulatory awareness, including GLP and ALCOA principles. Experience with electronic data capture for nonclinical studies. Basic knowledge of the drug development process. Required Skills Chemical Safety Communication Detail‑Oriented Experimentation Laboratory Maintenance Laboratory TechniquesRegulatory Awareness Standard Operating Procedure (SOP) Teamwork Preferred Skills Good Laboratory Practices (GLPs) Pharmaceutical Sciences Toxicology Benefits We offer a comprehensive package of benefits. Available benefits include medical, dental, vision, healthcare insurance, retirement benefits (401(k)), paid holidays, vacation, and compassionate and sick days. Salary Range $87,300.00 - $137,400.00. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable. Equal Employment Opportunity We are committed to inclusion and provide equal opportunities to all employees and applicants for employment. We prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit EEOC Know Your Rights. We are proud to embrace a diverse, inclusive environment. #J-18808-Ljbffr Merck & Co.