DESCRIPTION

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, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.

REQUIREMENTS

• PhD from an accredited institution in chemistry or related field with greater than five (>5) years of industry experience; or
• MS from an accredited institution in chemistry or related field with greater than ten (>10) years of AH industry experience.
• Considerable experience (greater than five (> 5) years) in veterinary research & development
• Research methodology experience.
• A minimum of five (5) years of broad experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization or equivalent combination of education and experience.
• Demonstrates a broad knowledge of field
• Hands-on experience with PK and Human Food Safety studies, estimation of exposures and drug concentrations, validation, method development and sample analysis.
• Knowledge of basic principles of PK and metabolism, as well as the relevance in the veterinary drug development.
• Solid understanding of chemistry and related fields contributing to an understanding of the basic principles of chromatography, mass spectroscopy and sample extraction methods.
• Able to effectively work in an international and cross-functional matrix environment
• Experience in analyzing literature and technology trends in bioanalytical chemistry.
• Experience with planning, conducting, reporting, analyzing and interpreting bioanalytical studies
• Experienced in project/program management.
• Independently develop method and performing sample analysis without supervision, act as study director, report writing and participate in method demo and method trial.
• Influencing departmental direction with knowledge of technology trends
• Demonstrates Industry-leading knowledge of field.
• Demonstrates knowledge of the pharmaceutical life cycle process.
• Go-to expert in the bioanalytical or metabolism area. Work on the project subteams.
• An analytical thinker. Excellent skills in understanding data and scientific decision processes, and in interpreting and reporting these data in well-supported conclusions targeted at achieving project objectives.
• Exhibits business and technical knowledge.
• Outstanding communication skills for effective oral and written communication in an inter-disciplinary and international environment.
• Outstanding interpersonal skills.
• A collaborative team player.
• Possesses a customer service orientation, delivering results and executing in a fast and focused manner.
• Exceptional planning and organizational skills with a quality orientation.
• Strives for business process excellence.
• Accepts accountability and ownership.
• Exhibits integrity and trust.
• Strong leadership skills. Able to mentor others within the global bioanalytical team without formal authority.
• A problem solver.
• Fosters innovation and drives change
• Responsible for direct reports including recruiting, managing, mentoring and developing scientific staff.English: Fluent (read, write and speak).

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

• GI_US92

DUTIES & RESPONSIBILITIES

Independently planning strategies for studies to reach goals and milestones. Designs and executes experiments or studies that follow templates, or creates improved and novel study designs that lead to new approaches for supplying product attributes or product goals. Fulfills a role as a subject matter expert in representing his/her function and providing communication on project core teams. Contributes technical approaches and scientific support to regulatory affairs in meeting regulatory requirements. The primary scope of responsibility is as a technical leader within their immediate function and secondarily within a multidisciplinary project team. Responsible for providing expertise in the areas of Mass Spectrometry, Ultra High Performance Liquid Chromatography, plasma and tissue sample preparation, bioanalytical method development and validation. Conducts residue analysis for pharmacokinetic, metabolism, human food safety, efficacy and safety studies to support the development of new products and the maintenance of existing products. Contributes to project and task force teams and functions as Study Director or Sponsor Representative for BIAH studies. Responsible for the generation and interpretation of scientific data leading to a better understanding of the pharmacological activity and safety profile of the active substances and for product registrations. Responsible for overseeing junior scientists. Manages laboratory activities.