Senior Scientist I

Description: Under the general guidance of a more senior staff member or Department Head, the individual is responsible for developing and validating robust analytical methods to support testing of APIs, excipients, raw materials and finished products. Additionally, the individual will perform routine and non-routine testing of developmental and investigation samples.  The individual is expected to work under GLP/GMPs and serve as a Study Director on GLP studies or analytical project leader, as appropriate   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: Develops, validates, and transfers robust analytical methods for testing of raw materials, excipients, APIs and finished products. Prepares protocols, memos, reports, and regulatory documents. Records, evaluates, interprets and summarizes technical data. Performs routine and non-routine testing of developmental and investigation samples, and instrument troubleshooting Acts as a Principal Investigator or Study Director or  Analytical Project Leader, if needed. Provides technical expertise in planning, monitoring, and maintaining project timelines to meet business needs. Organizes and presents the results of work internally and externally. Functions as in-house consultant for areas of technical expertise and provide technical supervision to junior scientist as needed. Understands and complies with Safety, Good Laboratory Practices (GLPs), Company Affirmative Action, and Standard Operating Procedures and Policies. Must be able to shift priorities and projects, as company's needs change.  As needed, assists others as priorities change   Requirements: Ph.D. in analytical chemistry or related field from an accredited institution Expertise in chromatography and other modern analytical technologies. Knowledge of GLP/cGMP regulations, ICH/VICH guidelines, and compendia monographs/methods.  Good ability to work with others to accomplish project goals.   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 1811442
Salary Range: NA
Minimum Qualification
Not Specified years

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