Quality Control Specialist (Temp-to-Perm)

Jupiter Endovascular•Menlo Park, CA

5h•$35 - $45•Onsite

About The Position

This is a 4-month temporary assignment with the potential to convert to a permanent role based on business needs and performance. The Quality Control Specialist is primarily responsible for receiving, in-process, and final product inspections. The QC Specialist may also perform equipment calibration and maintenance coordination and environmental monitoring activities in accordance with established quality system procedures. This role also supports nonconforming product disposition, traceability, lot release, and other quality assurance activities as assigned. This is an in-office role.

Requirements

High school diploma or equivalent required.
Minimum of three years of experience in a medical device manufacturing environment required.
Proficiency with word processing and spreadsheet software required.
Full professional proficiency in English required.

Nice To Haves

Startup or small-company experience preferred.
Catheter manufacturing experience preferred.
Experience reading and interpreting engineering drawings, specifications, and statistical sampling plans.
Experience using dimensional and visual inspection equipment, including microscopes.
Strong hand-eye coordination, manual dexterity, color vision, and visual acuity, corrected if necessary.
Ability to work under pressure, manage multiple deadlines, and maintain effective working relationships.
Strong attention to detail, organizational skills, and oral and written communication skills.

Responsibilities

Perform product receiving, in-process, and final inspections in accordance with written procedures, statistical sampling plans, engineering drawings, and product specifications, documenting nonconforming products as appropriate.
May administer the equipment calibration and maintenance system, environmental monitoring program, and bioburden monitoring program, including coordination with subcontracted service providers.
Coordinate or lead nonconforming product reviews, including Material Review Board activities and NCR/NCMR disposition, to support timely product decisions.
Maintain quality system logs, records, and filing systems, and ensure accurate traceability of components and finished products.
Maintain and operate inspection and test equipment, and provide input on inspection methods and quality procedures.
Support corrective and preventive action activities, supplier evaluations, and supplier performance monitoring.
Review product lot history records and support lot release to finished goods inventory, as applicable.
Support finished goods shipping and commercial release activities, as applicable.
Contribute to improvements in quality system procedures and work instructions related to areas of responsibility.
Train and advise other employees on quality-related requirements and ensure effective communication across functions.
Represent areas of responsibility during internal and external quality audits and support audit readiness.

Benefits

Competitive pay with performance incentives and equity opportunities.
Comprehensive, top of the market medical, dental, and vision coverage focused on meaningful premium support and smart savings.
Top tier 401(k) with a best in-class plan design which includes strong employer contributions.
Short and long-term disability.
Life insurance.
Commuter benefits.
Wellness support.
Healthy paid time off policy.
Company holidays.
Company-provided lunches.
Thursday socials.
Monthly potlucks.
Company events.
Volunteer opportunities.