Quality Engineer (Electromechanical Medical Device)

Company: AbbVie
Location: Pleasanton
Posted on: June 27, 2025

Job Description:

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn . Job Description Key Responsibilities Responsible for Supplier Quality Management cycle. Primary contact with suppliers on all quality related issues during both supplier maintenance & supplier selection process. Oversee supplier quality management activities & continuous improvement initiatives with suppliers. Plan & lead required supplier audits. Establish & maintains supplier quality metrics, scorecards, & trending. Generate quality plans & define risk control measures for continuous improvement. Conduct Design of Experiments (DOE) & Process Characterization for process optimization &/or improvement by conducting analyses using statistical techniques, including Gage Repeatability & Reproducibility (Gage R&R), Tolerance intervals, & Process Capability assessments with Cp or Cpk Lead or support design activities including design verification, validation, specification setting & justification, test method development, usability engineering, & risk management. Plan & conduct product & process verification & validation, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), & Process Performance Qualification (PPQ). Qualifications Education & Experience Must possess a Bachelors degree in engineering (mechanical, industrial, chemical, electrical), or other technical discipline. Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year of related work experience: conducting analyses using statistical techniques, including Gage Repeatability & Reproducibility, Tolerance intervals, & Process Capability assessments; executing Installation Qualification, Operational Qualification, Performance Qualification, & Process Performance Qualification; supporting quality system management, process controls, & Corrective Actions/Preventative Action systems by applying essential quality tools & statistical technique including: 8D, 5-Whys, 6M, SPC, DoE, & Fishbone diagram; reading & interpreting mechanical drawings & GD&T performing daily assigned tasks in compliance with FDAs Quality System Regulation (QSR), ISO 13485, ISO 14971, MDR, & MDSAP; performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & working in a cross-functional team, in a multisite corporation, preparing & delivering reports &/or presentations to scientific & business audiences, including executive team, both orally & in writing. Work experience may be gained concurrently. Additional Information Salary Range:$108,393.48 - 122,000.00 per year. Apply online at https://careers.abbvie.com/en send resume to Job.opportunity.abbvie@abbvie.com . Refer to Req ID: REF41154L We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Keywords: AbbVie, Redwood City , Quality Engineer (Electromechanical Medical Device), Engineering , Pleasanton, California