P
Penumbrainc3mo ago
$30 – $40/yr
Quality Assurance Engineering Specialist I
Quality Assurance SpecialistLaboratory & Life Sciences
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Quick Summary
Overview
General Summary The Quality Assurance Engineering Specialist I will support quality engineering activities to ensure the compliance of these systems with domestic and international regulations.
Technical Tools
Quality Assurance SpecialistLaboratory & Life Sciences
General Summary
The Quality Assurance Engineering Specialist I will support quality engineering activities to ensure the compliance of these systems with domestic and international regulations. They will follow standards and procedures in analyzing data from which conclusions can be readily obtained.
Specific Duties and Responsibilities
• Assemble sterile loads and complete associated documents for sterilization and product release. *
• Complete sample submission forms for shipping and testing. *
• Verify and document accuracy of sterilization process, biological test results, and completion of Device History Records (DHRs). *
• Communicate with sterilization facility and test laboratories as needed.
• Perform ongoing data entry, review, and analysis of data to support statistical process control. *
• Maintain and control quality record files and archived records. *
• Interface with other internal departments, customers, and suppliers on quality-related issues. *
• Assist in various other Quality Specialist tasks as needed.
• 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
Position Qualifications
Minimum education and experience:
• Bachelor’s degree in a scientific or engineering discipline with 1+ years of quality systems experience in regulated device or pharmaceutical environment or an equivalent combination of education and experience
Additional qualifications:
• Excellent oral, written, and interpersonal communication skills
• Problem solving and documentation skills
Location and Pay:
Alameda, CA
Starting Base Salary is $30.00 to $40.00/ per hour
Working Conditions
• General office, production, and cleanroom environments.
• Willingness and ability to work on site. May have business travel from 0% - 5%
• 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.
Listing Details
- Posted
- January 7, 2026
- First seen
- March 26, 2026
- Last seen
- April 21, 2026
Posting Health
- Days active
- 26
- Repost count
- 0
- Trust Level
- 34%
- Scored at
- April 21, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
Salary
$30 – $40
per year
External application · ~5 min on Penumbrainc's site
Please let Penumbrainc know you found this job on Jobera.
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Quality Assurance Engineering Specialist I$0k–$0k