Apply on Employer Site

Penumbra, Inc. · 23 hours ago

Manufacturing Engineer II

Alameda, CA

Full-time

Onsite

Entry, Mid Level

$95K/yr - $127K/yr

1+ years exp

Penumbra is a global healthcare company focused on innovative therapies. They are seeking a Manufacturing Engineer II to provide manufacturing technology solutions, support continuous improvement in production, and work cross-departmentally to resolve production issues.

Medical Device

H1B Sponsor Likely

Responsibilities

Solve complex 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

Suggest independent recommendations for project approach, scope, and tactics

Support production; Creating and maintaining product and process documentation; Monitor process and equipment performance and identify and implement process improvement activities to increase/optimize yield, efficiency, and/or throughput

Demonstrate an understanding of quality, operational, and financial systems, company products and customer requirements and how the product or project impacts the objectives of the business. Demonstrate an understanding of how other functional groups within the company are impacted by projects at hand and can impact the project or product results

Design fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the production line. Perform equipment qualifications

Test processes, equipment, raw materials, and product. Perform process validations. 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 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

Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures

Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company

Ensure other members of the department follow the QMS, regulations, standards, and procedures

Perform other work-related duties as assigned

Qualification

Manufacturing engineeringProcess improvementRoot cause analysisFDA regulationsLean manufacturingStatistical techniquesTraining skillsProject planningComputer proficiencyCommunication skillsTeam collaborationDocumentation skillsProblem-solvingInterpersonal skillsDetail-orientedTechnical writing

Required

Bachelor's degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree with 1+ years relevant engineering experience, or an equivalent combination of education and experience

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

Benefits

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

Paid sick time in compliance with applicable law(s)

Company

Penumbra, Inc.

Glassdoor3.3

Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies.

Founded in 2004

Alameda, CA, US

1001-5000 employees

http://www.penumbrainc.com

H1B Sponsorship

Penumbra, Inc. has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2025 (30)

2024 (42)

2023 (48)

2022 (43)

2021 (36)

2020 (26)