General Summary
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust
solutions that commercialize new products and that support continuous improvement in production.
Project opportunities are designed to develop professional work knowledge and abilities and to support
the efforts and projects that have global importance to the success of the business. Area of work involves
manufacturing processes with interaction between production and cross-departmental engineering
groups in resolving problems encountered on the production floor and across the business. A person in
this role specializes in the design, development, evaluation, selection, and ordering of the equipment that
is most appropriate and cost-effective for the manufacture of company products. Evaluates, selects, and
applies exciting engineering techniques, procedures, and criteria, using judgment in developing and
implementing adaptations and modifications on the production line and to quality systems.
Specific Duties and Responsibilities
As assigned by a project team leader or a manager or as business needs dictate, perform any of the
following:
• Solve problems and implement innovative solutions. *
• Execute detailed root cause analysis and recommend vetted solutions. *
• Communicate and explain problems and solutions cross-functionally and interdepartmentally. *
• Approach problems from a detail-oriented perspective. *
• Support production; Creating and maintaining product and process documentation; Monitor
process and equipment performance and identify and implement equipment-related process
improvement activities to increase/optimize yield, efficiency, and/or throughput. *
• Assist with the design, development, installation, modification, upgrade, and maintenance of
manufacturing equipment. Study equipment performance and reliability. *
• Provides technical support to the manufacturing equipment repair and process engineering
organizations. *
• Design fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the
production line. Perform equipment qualifications. *
• Test equipment processes. Perform process validations as appropriate. Author protocols to
execute tests, 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 project. *
• Develop specifications of a product, process, or piece of equipment. *
• Develop, characterize, and optimize processes using statistical techniques and engineering
knowledge and experience. *
• Coordinate with the appropriate suppliers and other external resources needed in developing and
implementing equipment-related process improvement plans. *
• Participate in project planning and scheduling. *
• Train assemblers, quality control and technicians, as necessary, on processes, equipment, and
documentation. *
• Perform other activities requiring knowledge of principles and techniques commonly employed in
the specific area of projects.
• Understand the relevant security, privacy and compliance principles and adhere to the
regulations, standards, and procedures that are applicable to the Company. *
• Adhere 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 work-related duties as assigned.
*Indicates an essential function of the role
Position Qualifications
Minimum education and experience:
• Bachelor’s degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial
Engineering or related field, or an equivalent combination of demonstrated performance,
education, and experience
Additional qualifications:
• 1+ year relevant engineering experience preferred
• Engineering experience in a manufacturing environment recommended, medical device industry
preferred
• Excellent written, verbal, and interpersonal communication skills required
• Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing
processes desired
• Proficiency in Word, Excel, PowerPoint, Access, and other computer applications required
Working Conditions
• General office, laboratory, and cleanroom environments
• Business travel from 0% - 5%
• 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.
Location and Salary:
• Roseville, CA
• Starting Base Salary is $68,680.00 to $89,580.00
The above statements are intended to describe the general nature and level of work being performed by
people assigned to this classification. They are not intended to be construed as an exhaustive list of all
responsibilities, duties, and skills required of personnel so classified
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.
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.
