As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems.
What You'll Work On
Solve complex problems and implement innovative solutionsExecute detailed root cause analysis and recommend vetted solutionsCommunicate and explain problems and solutions cross-functionally and inter-departmentallyApproach problems from a detail-oriented perspectiveSuggest independent recommendations for project approach, scope, and tacticsSupport production needsCreate and maintain product and process documentationMonitor process and equipment performance and identify and implement process improvement activities to increase/optimize yieldDesign fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the production lineTest processes, equipment, raw materials, and productPerform process validationsAuthor protocols to execute tests and write reports and make conclusions and/or recommendations based on test results Plan, schedule, conduct, and coordinate detailed phases of engineering work as part of a project or as a total projectDevelop specifications of a product, process, or piece of equipmentDevelop, characterize, and optimize processes using statistical techniques and engineering knowledge and experienceCoordinate with the appropriate suppliers and other external resources needed in developing and implementing process improvement plansParticipate in project planning and schedulingTrain assemblers, quality control and technicians, as necessary, on processes, equipment, and documentationComply with quality system regulations, standards and proceduresAdhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures.Ensure other members of the department follow the QMS, regulations, standards and procedures.Perform other activities requiring knowledge of principles and techniques commonly employed in the specific area of projects.What You Bring
A passion for tackling and solving technical problems preferredThe ability to communicate complex issues in a clear, compelling manner, both orally and in writing preferredProven work history of growing within an organization, learning its systems, and showing initiative preferredProven track record of solving problems creatively preferredMedical device experience strongly preferredProven knowledge of FDA regulations, lean manufacturing, and/or materials and manufacturing processes preferredBS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required
Working Conditions
General office environment. Business travel from 0% - 10%. Potential exposure to blood-borne pathogens. Requires some lifting and moving of up to 25 pounds. The employee is frequently required to stand, walk, sit, and reach with hands and arms, and to use a computer, sitting for extended periods. Specific vision abilities required by this job include the ability to read, close vision, distance vision, color vision, peripheral vision, and depth perception.
Alameda, CAStarting Base Salary is $80,330.00/year to $104,780.00/year.Individual compensation will vary over time-based on factors such as performance, skill level, competencies, work location and shift.What We Offer
•A collaborative teamwork environment where learning is constant, and performance is rewarded.
•The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
•A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, an employee stock purchase plan, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).
Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc.
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws.
