Quality Electrical Development Engineer II

Penumbra, Inc.; San Francisco (CA); On-site; USD 95,000 - 127,000; Full time

Benefits offered by this job

Generous benefits package

401(k) with employer match

Paid parental leave

Job summary

A leading medical device company is seeking a Quality Electrical Development Engineer II in San Francisco, California. This role involves collaborating on product development, ensuring PCB function verification, and interfacing with other engineering teams on quality-related issues. Candidates should have a relevant degree and a minimum of 2 years of quality engineering experience, particularly in regulated environments. The company offers a generous benefits package and promotes a collaborative team environment.

Qualifications

• 2+ years of relevant experience in quality engineering, preferably in a regulated industry.
• Experience with electronic devices and PCBAs.
• Ability to work in diverse environments.

Responsibilities

• Collaborate in development and qualification activities for products.
• Perform PCB function verification to validate design specifications.
• Interface with engineering departments on quality-related issues.

Skills

Quality engineering experience

Familiarity with QSR and ISO regulations

Excellent communication skills

Proficiency with MS Office

Education

Associate’s or Bachelor's degree in Engineering

Job description

Quality Electrical Development Engineer II

Base pay range: $95,000.00/yr - $127,000.00/yr

Responsibilities

• Collaborate in the development and qualification activities for new and existing products*
• Perform PCB function verification to ensure all functions meet design specifications, validating critical parameters such as power and signal integrity margins
• Maintain and track critical hardware PCB issues, document findings, and ensure effective communication with relevant stakeholders
• Collaborate in the development of testing and inspection methodology and documentation for new and existing products*
• Collaborate on Quality Objective teams*
• Design and install QC process sampling systems, procedures, and statistical techniques*
• Design or specify inspection and testing mechanisms and equipment*
• Perform failure analyses and defect investigations *
• Analyze production limitations and standards *
• Recommend revision of specifications *
• Interface with other engineering departments within the company, customers, and suppliers on quality related issues*
• Collaborate in the development of standard operating procedures*
• Facilitate and perform internal audits*
• 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
• *Indicates an essential function of the role

Qualifications

• Associate’s or Bachelor's degree in Engineering, a Life Science, or a related field, with 2+ years of quality engineering or relevant experience, preferably in a medical devices or regulated industry environment, or equivalent combination of education and experience.
• Familiarity with QSR, ISO and other applicable regulations and laws required.
• Engineering experience in a manufacturing environment recommended, medical device industry preferred.
• Experience with electronic devices and/or PCBAs.
• Excellent verbal, written, and interpersonal communication skills.
• Proficiency with MS Word, Excel, and PowerPoint.

Working Conditions

• General office, laboratory, and cleanroom environments.
• Potential exposure to blood-borne pathogens.
• Requires some lifting and moving of up to 25 pounds.
• Must be able to move between buildings and floors.
• Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.
• Must be able to read, prepare emails, and produce documents and spreadsheets.
• Must be able to move within the office and access file cabinets or supplies, as needed.
• Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.

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).

Equal Opportunity Statement

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.

If you reside in the State of California, please also refer to Penumbra’s Privacy Notice for California Residents.

For additional information on Penumbra’s commitment to being an equal opportunity employer, please see Penumbra’s AAP Policy Statement.

Seniority Level

Associate

Employment Type

Full‑time

Job Function

Medical Equipment Manufacturing

Location and Salary

Sunnyvale, CA
Salary: $95,000 to $127,000