Quality Engineer I

Penumbrainc; Roseville (CA); On-site; USD 72,000 - 94,000; Full time

Benefits offered by this job

Generous benefits package

Collaborative teamwork environment

Emphasis on continuous learning and performance rewards

Job summary

Penumbrainc is seeking a Quality Engineer I in Roseville, CA. The role focuses on ensuring the quality of Penumbra's medical devices through technical problem-solving and adherence to quality standards.

Candidates should have a degree in engineering or a related field and experience in manufacturing or labs. The position offers competitive compensation between $72,000 and $94,000, and extensive benefits including medical and paid time off.

Qualifications

• 1+ years of experience in a manufacturing or laboratory environment strongly preferred.
• Ability to thrive in a fast-paced work environment.
• Passion for working in collaborative and dynamic teams.

Responsibilities

• Provide input in the design control process.
• Identify and drive areas of opportunity for process improvement.
• Determine root-cause of quality assurance issues.

Skills

Communication skills

Problem-solving

Team collaboration

Education

Bachelor’s or Master’s degree in an engineering or scientific discipline

Job description

General Summary

As a Quality Engineer I, you will be charged with the quality behind Penumbra's game‑changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements.

What You’ll Work On

• Provide valuable input in the design control process and help in developing and launching new products
• Independently provide knowledge of Penumbra Quality Management System as it pertains to sustaining manufacturing operations as well as dealing with supplier quality and developing new products
• Identify and drive areas of opportunity for process improvement, yield improvement, and cycle time reduction
• Determine root‑cause of in‑process quality assurance issues
• Experience on production lines manufacturing high performing products
• 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 activities requiring knowledge of principles and techniques commonly employed in the specific area of projects.

What You’ll Bring

• 1+ years of experience in a manufacturing or laboratory environment strongly preferred
• Proven ability to thrive in a fast‑paced work environment where navigating grey areas is a welcomed challenge preferred
• A Bachelor’s or Master’s degree in an engineering or scientific discipline required
• Clear and concise written and oral communication skills required
• A passion for working in collaborative and dynamic teams with feedback‑rich culture preferred

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.

Location and Pay

• Roseville, CA
• $72,000 to $94,000
• 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, 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.

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.