**Description** Under the general direction of a more senior staff or director, the incumbent is primarily responsible for planning and conducting formulation research and development activities in regulated environment with little technical guidance on laboratory techniques. May provide direction to other professional personnel. Expected to initiate new projects within an existing program. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. **Duties & Responsibilities** • Planning and conducting formulation research and development activities in a regulated environment. • Preparation of oral and parenteral dosing formulations of test compounds for non-clinical exploratory and GLP toxicology studies. Coordinate activities with CRO partners. • Compile method templates/ batch formulation records/ancillary documents and prepare formulations for tox studies in the regulated GLP environment. • Maintain logistics of incoming and out-going test item and vehicle/diluent shipment requests to enable in-house and CRO study execution. Receive, transfer or ship test/control item (frozen, refrigerated or room temperature). Maintain inventory records. • Ensure proper completion of study-related documentation on time. Ensures quality control and regulatory compliance of all study-related documents from the group. • Write, review and update Standard Operating Procedures. • Respond or review responses to QA audits. Complies with all applicable regulations, performing all work in a safe manner. Maintains proper records in accordance with SOPs and policies. • Initiates and completes routine procedures in an independent and efficient manner; Troubleshoots effectively and solves scientific problems independently; Operates lab equipment and is independently responsible for maintenance • Represent Pre-clinical Formulation Development on multi-disciplinary project teams. **Requirements** **Scientist III:** Master’s degree with 3+ years of experience in related scientific discipline or Bachelors' degree with 7+ years of related scientific discipline or equivalent experience in related field. **Scientist II:** Bachelors' degree with 3+ years’ experience in related scientific discipline or Master’s degree in related scientific discipline or equivalent experience in related field. **Desired requirements for both levels:** • Experience in formulation development and preparation of multiple dosage forms. • Fundamental understanding of pharmaceutical product development and formulations coupled with hands-on experience with handling pharmaceutical materials, excipients and oral dosage forms and parenterals. • GxP knowledge and experience. • Attention to details; Ability to multi-tasks and prioritize • Ability to operate laboratory equipment with independence • Demonstrate written and verbal communication skills • Concise and accurate reporting of technical data and interpretation thereof • Proven problem-solving ability • No known allergies to animals • Ability to lift up to 30 lbs. and work in a standing position for extended duration (~2 hrs.) with periodic breaks • Must be able to wear respiratory and eyewear protection devices • Must be able to access laboratory equipment on bench tops or equivalent while using both hands to perform manual dexterity operations **Eligibility Requirements:** Must be legally authorized to work in the United States without restriction. Must be willing to take a drug test and post-offer physical (if required). Must be 18 years of age or older. **Compensation Data** This position offers a base salary typically between $75,000 and $122,000.  The position may be eligible for a role specific variable or performance-based bonus and or other compensation elements.  For an overview of our benefits please click here. (https://www.boehringer-ingelheim.com/us/careers/benefits-rewards) All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.