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 several 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.
The Senior Principal Engineer, Project Management will develop and manage the execution of multiple complexes, high value capital investment projects to maintain budget, schedule, safety record, and project quality.
Project Development and Management:
Project Controlling and General Administrative Support:
BS degree in construction-related engineering (engineering management, civil, mechanical, etc.) or hard science (chemistry, biology, etc.) or related field required. OR Master's Degree in Engineering/Project Management or Business Administration or currently pursuing preferred. Five-plus (5+) yrs experience of relevant experience in construction-oriented project management. Strong organization, leadership, communication skills, presentation and negotiation skills. Strong team orientation and ability to work cross functionally with various groups such as Safety, Quality, Maintenance, Purchasing, Industrial Development, R&D, and Manufacturing. Ability to execute multi-discipline assignments and ability to master new skills quickly. Experience using Excel, Word, PowerPoint, Outlook, Visio, Microsoft Project, and AutoCAD.
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.
PMP, EIT or strong desire to pursue Lean Six Sigma Certification Five (5) years in the biopharma industry Experience with cGMP compliance and related quality systems Experience with Lean and Six Sigma tools and methodologies Working knowledge of the current editions of following references: USDA – Manual 242.1 – ARS Facilities Design Standards CDC / NIH – Biosafety in Microbiological and Biomedical Laboratories (BMBL) NRC – Guide for the Care and Use of Laboratory Animals 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.