DescriptionAs 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 SR Engineer, Process has the responsibility of providing manufacturing support of current processes and process improvement initiatives as well as providing support to Capital Project initiatives to install new equipment, facilities, and/or utilities.DescriptionAs 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 SR Engineer, Process has the responsibility of providing manufacturing support of current processes and process improvement initiatives as well as providing support to Capital Project initiatives to install new equipment, facilities, and/or utilities.Duties & ResponsibilitiesFacilitates changes to existing production processesAccountable for installation, commissioning, start-up of new equipment and changes to existing equipmentAssists with validation of new equipment and changes to existing equipment including document generationActs as change control owner for equipment and process improvement projects. Coordinate change control meetingsAssigns action items for change controlAccountable for change control action items and documentation. Documentation includes drawings, functional specifications, detailed design specifications, Turn-over-packages, material specifications, and other documentation as requiredSupports troubleshooting product and equipment issues in production areas such as biomanufacturing, formulation and filling, lyophilization and packagingIdentifies improvements to manufacturing process. Improvements may include mechanical, automation, or workflowWorks with manufacturing and capital engineering on the development of future capital projects and on the development of requirements for the projectResponsible for User Requirement Specification developmentAssists cross functional teams in the execution of small-scale capital projects up to around $500,000, process improvement projects, continuous improvement projects, and equipment improvement projectsOn larger capital projects, the engineer will be responsible for to ensuring process requirements are communicated and built into the equipment/system design. The engineer will develop specifications (user, functional, and detailed design) for equipment and automation of the equipmentDevelops and maintains overall knowledge of facility processes and productsProvides training on process and/or equipment modifications as required for new or existing equipment/processesActs as Subject Matter Expert for production equipment and processes for Capital Engineering, Production, Business Process Science, Quality Assurance, and MaintenanceRequirementsBachelor of Science Degree in Engineering from an accredited school with one to three (1-3) years applicable experience in a GMP environment or Bachelor´s degree with three to five (3-5) of engineering or scientific experience outside of a GMP environmentIn lieu of years of experience, Master´s Degree in relevant field from an accredited school with one (1) year experience in a GMP environment or at least one (1) year of engineering or two (2) years of scientific experience outside of a GMP environmentAt least one (1) year of experience leading projects preferableCompetencies:Effective verbal and written communication with all levels of corporate and local management and employeesAbility to plan, schedule, organize, prioritize, and coordinate project activitiesAbility to understand and work within a regulated environmentExperience with GAMP Automation practices and documents preferredAbility to function in a leadership role as well as in a team environmentAbility to manage multiple projects at one timeSkills:Analytical ThinkingData collection and analysisCommunicationCustomer FocusData-driven Decision MakingPlanning and OrganizingTeamworkConceptual / Analytical Thinking ScopeDelivering ResultsLeadershipDesired Skills, Experience And AbilitiesOur CompanyWhy Boehringer Ingelheim?With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.Want to learn more? Visit
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