{"schemaVersion":"jobsearcher.job.v1","id":"d9c6dac97d8e7c1df752d2f8","url":"https://jobsearcher.com/jobs/d9c6dac97d8e7c1df752d2f8","canonicalUrl":"https://jobsearcher.com/jobs/d9c6dac97d8e7c1df752d2f8","title":"Sr Engineer","description":"ENGINEERING SR ENGINEER, PRODUCT STEWARDSHIP: St. Jude Medical, an Abbott Labs Co. in Sylmar, CA. Lead & coordinate Product Stewardship project lifecycle inclini-tiation, planning, implementation, tracking & closure to achieve regulations compliance & org goals. Bachelors or foreign equiv in Mechanical Eng or in rltd eng fld of study w/ min. 7 yrs of rltd progressive pro eng exp. Alternatively will accept Masters w/ min. 5 yrs of rltd pro eng exp. Each alt req must possess min 5 yrs of pro exp in: (i) coordinating Product Stewardship project lifecycle incl initiation, planning, implementation, tracking & closure; (ii) regulatory material compliance requirements w/ country-specific regulations (REACH, China ROHS, EU MDR & California Prop65); (iii) identifying & assessing potential risks associated w/ product design, mfg & end-of-life mgmt, & implementing strategies to minimize environmental impact of products & processes; (iv) developing cont. improvement opportunities for processes & projects; (v) conducting periodic reviews of procedures & Detailed Work Instructions (DWIs) for Risk Management & product development in compliance w/ EN ISO 14971 & ISO 13485 standards & make improvements as needed to meet regulation requirements; & (vi) working w/ suppliers to get required material info act on regulation compliance regarding materials. Employer will accept any suitable combo of education, training, or exp. An EOE. 40 hrs/wk. $142,355 - $180,000/year. Send resumes to AbbottJobs1@abbott.com or by mail to Abbott Laboratories, Attn: 26J14A, Willis Tower, 233 S. Wacker Dr., Floor 26, Dept. 32, Chicago, IL 60606. Refer to ad code: SJM-0083-ES.recblid hr1scwjrdhumata4ecxz5i6xo4u4vfPDN-a23d5118-949f-491c-8c75-0f2804654378","company":"Talentally","rawCompany":"talentally","city":"Altadena","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-01T09:53:32.709Z","occupations":[{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2141.00","title":"Mechanical Engineers","slug":"mechanical-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr Engineer","description":"ENGINEERING SR ENGINEER, PRODUCT STEWARDSHIP: St. Jude Medical, an Abbott Labs Co. in Sylmar, CA. Lead & coordinate Product Stewardship project lifecycle inclini-tiation, planning, implementation, tracking & closure to achieve regulations compliance & org goals. Bachelors or foreign equiv in Mechanical Eng or in rltd eng fld of study w/ min. 7 yrs of rltd progressive pro eng exp. Alternatively will accept Masters w/ min. 5 yrs of rltd pro eng exp. Each alt req must possess min 5 yrs of pro exp in: (i) coordinating Product Stewardship project lifecycle incl initiation, planning, implementation, tracking & closure; (ii) regulatory material compliance requirements w/ country-specific regulations (REACH, China ROHS, EU MDR & California Prop65); (iii) identifying & assessing potential risks associated w/ product design, mfg & end-of-life mgmt, & implementing strategies to minimize environmental impact of products & processes; (iv) developing cont. improvement opportunities for processes & projects; (v) conducting periodic reviews of procedures & Detailed Work Instructions (DWIs) for Risk Management & product development in compliance w/ EN ISO 14971 & ISO 13485 standards & make improvements as needed to meet regulation requirements; & (vi) working w/ suppliers to get required material info act on regulation compliance regarding materials. Employer will accept any suitable combo of education, training, or exp. An EOE. 40 hrs/wk. $142,355 - $180,000/year. Send resumes to AbbottJobs1@abbott.com or by mail to Abbott Laboratories, Attn: 26J14A, Willis Tower, 233 S. Wacker Dr., Floor 26, Dept. 32, Chicago, IL 60606. Refer to ad code: SJM-0083-ES.recblid hr1scwjrdhumata4ecxz5i6xo4u4vfPDN-a23d5118-949f-491c-8c75-0f2804654378","datePosted":"2026-08-01T09:53:32.709Z","dateModified":"2026-08-01T09:53:32.709Z","hiringOrganization":{"@type":"Organization","name":"Talentally","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Altadena","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d9c6dac97d8e7c1df752d2f8"},"url":"https://jobsearcher.com/jobs/d9c6dac97d8e7c1df752d2f8"}}