Quality Systems Engineer II - CAPA
Boston Scientific Corporation
Recruiter: Spencer Gregory HaleQuality Systems Engineer IIAbout the role:As a Quality Systems Engineer II, you will support the Corrective and Preventative Action (CAPA) process at Maple Grove, inclusive of nonconforming events. The Quality Systems Engineer II will support compliance of the CAPA Process to internal requirements and external regulations. This includes CAPA Investigations and Product/Material/System Nonconformances. This role partners closely with Maple Grove CAPA team members, investigation owners, and site leadership. They will provide mentorship to Quality team members and cross-functional stakeholders to enable high-quality investigations, robust root cause identification, and sustainable corrective and preventive actions.Work model, sponsorship, relocation:At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.Your responsibilities will include:Mentor cross-functional CAPA teams on:- root cause analysis, corrective action plans, and effectiveness verifications- using project management best practices to effectively coordinate activities, communicate progress, collaborate on key deliverables, and meet critical CAPA phase timelines- creating robust, compliant, and timely records, using the electronic CAPA database systemProvide guidance on nonconformance investigations to support appropriate scoping, risk assessments, corrections, and material/product containment (including physical segregation/identification).Provide continuous and rigorous assessment of CAPA activities and review of documentation throughout the CAPA lifecycle to ensure compliance with global BSC CAPA processes, FDA regulations, ISO 13485, and Medical Device RequirementsApply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve systemic quality issuesActs as an effective team member and/or leader in supporting quality disciplines, decisions, and practicesPartner with cross-functional stakeholders to drive standardization and adoption of best practices across sitesTeam member of subject matter experts relating to CAPA at the Maple Grove siteTrack actionable CAPA metrics and trends to ensure proper execution and effectiveness of the site CAPA programSupport Site, Regional, and Global CAPA initiatives, continuous improvement opportunities and/or projectsDrive continuous improvement and efficiencies to support a preventive quality cultureQualifications:Required qualifications:Bachelor's degreeMinimum of 2 years' experience in the medical device or pharmaceutical industryPractical understanding of nonconformance and CAPA regulatory requirements and best practicesUnderstanding of regulations/standards such as 21 CFR 820 and ISO 13485Experience leading or supporting cross-functional initiatives or projectsStrong problem-solving and root cause analysis skillsStrong communication and stakeholder management skillsAbility to make sound, risk-based decisionsPreferred qualifications:Minimum of 2 years' experience in Quality Systems and/or CAPA ManagementStrong interpersonal skills with the ability to collaborate effectively across Quality, Manufacturing, Engineering, Regulatory, and Supply Chain functionsHigh attention to detail, organizational skills, and a disciplined approach to compliance and documentationAbility to prioritize tasks effectively in a deadline-driven environmentProactive problem solver with a continuous improvement mindsetAbility to manage priorities in a fast-paced environment with strict regulatory timelinesHands-on Project Management experienceAble to work independently and as a contributing team memberContinuous improvement mindset with a passion for QualityRequisition ID: 634838Minimum Salary: $ 71500Maximum Salary: $ 135800The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
- Recruiter: Spencer Gregory HaleQuality Systems Engineer IIAbout the role:As a Quality Systems Engineer II, you will support the Corrective and Preventative Action (CAPA) process at Maple Grove, inclusive of nonconforming events. The Quality Systems Engineer II will support...SuggestedHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week
$71.5k
...Recruiter: Spencer Gregory Hale Quality Systems Engineer II About the role: As a Quality Systems Engineer II, you will support the Corrective and Preventative Action (CAPA) process at Maple Grove, inclusive of nonconforming events. The Quality...SuggestedHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week- ...Inspire Medical Systems is seeking a CAPA/Quality professional to lead corrective and preventive actions across internal and supplier processes. You will work with Development, Manufacturing, Marketing and IS to ensure CAPA activities align with Inspire procedures and...Suggested
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...arrhythmias, or irregular heartbeats. Supplier Quality Enginee r II drives improvement and corrective... ...in products. Provide input to Design Engineering on new component technology and assist... .... Will perform this job in a quality system environment. Failure to adequately...Work experience placementShift work$85k - $110k
...is looking to hire a senior quality engineer to join their team. This Sr Quality... ...handling, and related CAPA activities. They should also... ...Previous experience with Class II or Class III medical device contract... ...QMS (Quality Management System), GMP (Good Manufacturing...Contract work- Recruiter: Spencer Gregory HaleSenior Quality Systems EngineerAbout the role:The Senior Quality Systems Engineer provides technical leadership and subject matter expertise... ...:Lead and support QMS processes including CAPA, nonconforming events, internal audits, external...Hourly payWork at officeShift work3 days per week
$36 - $43 per hour
...market-leading provider of automated test systems and test fixtures for complex electronic... ...electrical, software, mechanical engineers, and project managers. Our systems are supported... ...by our customers as having world-class quality, reliability, and perceived value....Hourly payTemporary workFor contractorsH1bWork visa- ...Abbott in Minnetonka, MN, is seeking a Supplier Quality Engineer II to drive improvement and corrective action on supplier components. The... ...and 2–5 years of relevant experience, with a focus on quality systems, supplier relations, and problem solving. Join Abbott to advance...
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...disposables to fully integrated systems to precision components, our... ...responsible for operational quality input and deliverables for... ...lifecycle. Quality Assurance Engineers will also support development... ...implementation.Manage nonconformances and CAPAs from initiation through...Temporary workH1bWorldwide$75k - $112.6k
...stamping and device assembly. Learn more at Position Summary The Quality Systems Engineer will be responsible for providing core quality business... ...processes to include Engineering/Document Change Orders, CAPA, Management Review, Standards Library, Internal Audit, New Customer...Hourly payContract workTemporary workWork at officeLocal area- ...Description Summary: Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory... ...implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and...Contract work
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$43 - $52 per hour
...Job Description Job Title: Lead Quality Engineer Job Description The Lead Quality Engineer... ...will oversee day-to-day quality systems for a Class II medical device within a small, collaborative... ...Management System (QMS), including CAPAs, change reports, continuous...Contract workTemporary workWork at officeMonday to Friday$130k - $170k
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...therapeutic technology and they're looking to add a Senior Supplier Quality Engineer to their team.This is a highly visible role supporting a... ...manufacturing experience * Strong knowledge of supplier audits, CAPA, root cause analysis, and supplier development * Experience...- Recruiter: Spencer Gregory HaleSenior Supplier Quality Engineer - SFMDAbout the role:The Sourced... ...validations, and process validations.Quality System Champion:Collaborates with corporate and... ..., design controls, risk management, and CAPA.Ability to work independently; organized...Hourly payShift work
- ## Supplier Quality EngineerApply: Anoka, MN: Full time... ...a **Supplier Quality Engineer**. The **Supplier Quality... ...develop robust quality systems, resolve performance... ...and preventive action (CAPA) processes with suppliers... ...citizen or national; (ii) U.S. lawful, permanent...Permanent employmentFull timeContract workWork at officeLocal area
- ...For The primary emphasis of the Supplier Quality Engineer is to assist with managing product... ...materials and maintain and implementing quality system procedures for supplier evaluation. Use... ...auditing, complaint handling, and CAPA fulfillment. Participate in product design...Contract workFlexible hours
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...impact. A Day in the Life The Quality Engineering function partners across manufacturing... ...team focuses on strengthening quality systems advancing First Time Quality (FTQ) practices... ...is required. As a Quality Engineer II you will drive initiatives that improve...Full timeH1bWork at officeLocal areaImmediate startFlexible hours- ...providing mobility solutions for combustion engines, transmissions, hybrid applications, fuel... ...ADAS/AD, data intelligence, and embedded systems for all types of vehicles. Our mission is... ...looking for a Project Engineer II - Structural Analysis to provide technical...Full timeWork visa
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At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Description : Job Overview Works under the supervision of administrative division management to gain ...Work experience placementSummer workInternshipLocal area$75k - $90k
...dealing with the three major phases of Quality Management - Quality Planning/Prevention... ...supplier.Develop and maintain internal quality system, procedures, work instructions and... ...audit Safety audit etc.Follow up the EC(Engineering Change), SPCN(Supplier Process Change Notification...Temporary workWork at office$100k - $130k
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...OUTSIDE.Position Overview:You will lead quality engineering activities that support the ORV parts... ...strategies and tools that strengthen quality systems and Supplier Relationship Management.... ...activities, including PPAP, CAR and CAPA, PCR, Run-at-Rates, audits, DCR, and deviations...Full timeLocal area- ...Abbott, a global healthcare leader, seeks a Supplier Quality Engineer II for the Cardiac Rhythm Management division in Minnetonka, MN. You’... ...protocols, and reliability, mentoring staff and guiding moderate projects within a quality system environment. #J-18808-Ljbffr...
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