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Terumo BCT Engineer 2 - Sustaining in Lakewood, Colorado

Requisition ID: 29949At Terumo Blood and Cell Technologies, our 7,000+ global associatesproud to come to work each day, knowing that what we do impacts the lives ofpatients around the world.We make medical devices and related products that are used to collect,separate, manufacture and process various components of blood and cells.With our innovative technologies and service offerings, we touch apatient's life every second of every day and are committed to continuing toincrease the number of patients we serve.With some of the best and brightest minds in the industry, an unmatchedglobal footprint, comprehensive benefits and a distinct culture, TerumoBlood and Cell Technologies is a great place to work, grow and be part of ateam that is focused on making a difference. Consider joining our team andunlock your potential.Engineer Level 2 - SustainingJOB SUMMARYWork requires independent evaluation, selection and application of standardengineering techniques, procedures, and criteria, using judgment andingenuity in making minor adaptations and modifications to product.Assignments include device design and development, tests of materials,preparation of specifications, risk mitigation, research investigations,report preparation and other activities of limited scope. Duties are assignedto provide experience and familiarization with engineering methods,independent thinking, and company practices and policies.ESSENTIAL DUTIESWorks with cross functional teams to ensure product sustaining activities forreleased products are being completed in adherence to the Quality ManagementSystem. This includes, but is not limited to, gathering customerfeedback, evaluating requirements, modeling, prototyping, procuringtest samples, developing protocols and reports, evaluating and mitigatingdesign risk, and transferring changes to production.Manages projects including development of project scope and estimates,initiation of requests for capital when required, management of costs tobudget, and support of product documentation in accordance with acceptableengineering practices.Conducts studies and makes recommendations for the purchase and implementationof new technologies, practices, tools, and equipment to maximize siteeffectiveness.Prepares and reviews engineering/technical documents such as reports,SOP's, protocols, schedules and budgets, and vendor provided documentsand drawings.Ensures that designs are compliant with all Company policies and procedures aswell as all Local, State, and Federal directives, laws and regulations.Provides work direction to engineering support staff.Takes initiative and demonstrates inquisitive approaches to solve moderatelycomplex problems, indentifying problems, generating alternatives andrecommending solutions.Follows department processes and regularly makes recommendations on theseprocesses.Follows technical specification requirements, developing reports, chartsand graphs to support project recommendations and responds to questions fromtechnical staff members and management.Works cooperatively and effectively in a team environment or across teams toachieve common goals and results.Analyzes data and presents it in appropriate forums.Actively participates in Quality System and Good Laboratory Practicerequirements, particularly with respect to documentation.OTHER DUTIES AND RESPONSIBILITIESWork assignments may require additional development and a maturing orbroadening of in-depth engineering skill(s).May work with manufacturing, quality, regulatory, and other functionalgroups on development, process, and compliance issues.MINIMUM QUALIFICATION REQUIREMENTSEducationBachelor's degree or equivalent of education and experience sufficient tosuccessfully perform the essential functions of the job may be considered.Bachelor of Science Degree in Biomedical, Mechanical or ChemicalEngineering, preferred.ExperienceMinimum 2 years experience.Two years product development and/or product sustaining experience in themedical device indust