Quality Compliance Auditor II - Medical Device
Baxter International
Location: Round Lake, Illinois, United StatesCompany: Baxter International Inc.Posted: 2026-08-17Baxter International Inc. seeks a Quality Associate II within the Quality organization to uphold audit quality systems and regulatory compliance. You will manage internal audits, CAPA, inspections readiness, and mentor junior staff while driving continuous improvement.The role emphasizes GMP knowledge, strong analytical skills, and the ability to collaborate across plants and offices worldwide to ensure product safety and regulatory adherence. Applicants must be authorized to work in the U.S.#J-18808-Ljbffr
$88k - $121k
...one day to the next. As a Quality Associate II, you are unafraid of navigating... ...will independently manage compliance audit processes and serve... ...in Quality with a medical device / Pharma company or other... .... ASQ CQA and/or other auditor accreditation strongly preferred...Medical deviceOdd jobTemporary workWorldwideWork visaFlexible hours$88k - $121k
...same from one day to the next. As a Quality Associate II, you are unafraid of navigating through... ...for regulatory, product quality, and compliance impact; coordinate cross‑functional... ...regulated pharmaceutical, biotech, or medical device environment. Hands‑on experience with...Medical deviceOdd jobTemporary workWork at officeWorldwideWork visaFlexible hours$88k - $121k
...same from one day to the next. As a Quality Associate II, you are unafraid of navigating through... ...for regulatory, product quality, and compliance impact; coordinate cross-functional... ...regulated pharmaceutical, biotech, or medical device environment. Hands-on experience with...Medical deviceOdd jobTemporary workWork at officeWorldwideWork visaFlexible hours- ...health issues today and address the medical challenges of tomorrow. We... ...To work with AbbVie's Global Quality Organization to complete pharmaceutical, medical device and combination product complaints... ...~ Knowledge of Quality/Compliance management as well as regulations...Medical deviceFull timeTemporary workLocal area
- ...existing product packaging and packaging processes, supporting quality, regulatory compliance, continuity of supply, and cost-saving initiatives. The... ..., verbal, and presentation skills. Experience in the medical device, pharmaceutical, or healthcare industry. Knowledge of...Medical deviceFlexible hoursNight shift
$30 - $40 per hour
...Title: Engineer II, Packaging Location: Vernon Hills, IL Contract Term: 6+ Months Weekly 40.00 hours pay rate: $30-4... ...Need experience candidates only. Job Description Summary Medical Device packaging engineer with knowledge and experience in regulated packaging...Medical deviceContract workTemporary workFor contractorsFlexible hours- ...primarily with human factors, quality control, inventory... ...to ensure continued compliance to regulations and... ...leadersWork with internal auditors to develop programs to... ...projected products or devices.Qualifications•... ...pharmaceutical industry or medical device experience• BS...Medical device
- ...Title: Project Engineer II Duration: 12 months with possible... ...in pharmaceutical, medical device, combination product, or other... ...Design Control documents in compliance with applicable regulations.... ...stakeholders across human factors, quality, clinical, medical safety, development...Medical device
$20 - $22.91 per hour
...Title: Assembler Associate II Location: Abbott Park, IL... ...instructions, GMP requirements, and quality standards. Support... ...activities as needed. Maintain compliance with applicable regulatory... ...Qualifications Experience in medical device, pharmaceutical,...Medical deviceWeekly payFull timeContract workMonday to Friday- ...are seeking a detail-oriented and experienced Quality Assurance Specialist to support quality operations and compliance initiatives in a regulated environment. This... ...preferred Preferred Skills Experience in medical device, pharmaceutical, biotech, or healthcare...Medical deviceLive inWork at officeLocal area
$60k - $120k
...and training firm specializing in the medical device and combination products industry. We help... ...product development and ensure market compliance. We are seeking a dynamic and... ...Build and maintain relationships with R&D, Quality, and Regulatory teams to understand their...Medical devicePermanent employmentFull timeTemporary workRemote workFlexible hours- ...Responsibilities:Serves as the primary quality lead for project activities... ...driver for the quality and compliance aspects of the project.... ...proper integration and support of device regulations, drug regulations... ...of combination products, medical devices, and design controls....Medical device
- ...level Verification & Validation (V&V) activities for medical device products. The role involves planning and executing... ..., supporting design verification, and ensuring compliance with FDA, ISO 13485, and internal quality system requirements. Experience with infusion pump...Medical device
- ...Title - Sr. Validation Engineer Location - Round Lake IL Job Type - Contract Key Qualifications- 1) Experience in medical devices (probably infusion pumps) 2) strong system level V&V experience. 3) Ability to perform execution on validation activities....Medical deviceContract work
$105k
Embedded Software Engineer - Medical Devices Location: McHenry, IL (Hybrid - 3 days onsite) Salary... ...electrical, systems, manufacturing, quality, and regulatory engineering teams.... ...post‑market product maintenance Ensure compliance with quality and regulatory requirements...Medical deviceLocal area- ...issues today and address the medical challenges of tomorrow. We strive... ...with project, operations and quality objectives. Level of... ...laboratory diagnostics, medical devices, pharmaceutical, or similar industries... .... ~ Knowledge of quality / compliance management as well as...Medical deviceFull timeContract workTemporary workLocal area
$30 - $35 per hour
...Quality Assurance Compliance Specialist II Pay Range: $30/hr to $35/hr Location: North Chicago, IL 60064 Work Type: Onsite Contract Duration... ..., subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k)...Contract workTemporary work- ...Reference26-00744 Job Summary: Manager, Design Quality - Lifecycle Management responsible for... ...maintained on market while assuring compliance to local, divisional, and corporate... ...regulations worldwide. Products include medical devices and combination products, such as...Medical deviceContract workLocal areaWorldwide
- ...today and address the medical challenges of tomorrow.... ...Principal AI Engineer II will define and advance... ...risk-based approaches to compliance, GxP, data integrity,... ...responsible AI. Partner with Quality, Regulatory, Legal,... ..., healthcare, medical device, or life sciences....Medical deviceFull timeLocal area
- ...improve patient outcomes through cross‑functional collaboration on medical device development. You will guide design inputs and interface... ...teams to decompose complex system needs while aligning with quality and regulatory standards. The role requires a strong background...Medical device
- ...work cross-functionally with Quality, Regulatory, Operations, and... ...reportable events. Support compliance with FDA Quality System Regulations... ...Strong ability to interpret medical narratives, product... ...remediation experience in a medical device or pharmaceutical environment...Medical device
- ...with 3–5+ years in a Director-level Operations role within Medical Devices or other regulated industries.Proven experience leading... ...success delivering measurable results while maintaining high quality and compliance standards.Strong P&L ownership and financial discipline...Medical deviceFull timeShift work
$112k - $154k
...general direction to verification engineering staff. Ensures that quality is built into the design during new product development.... ...Engineering or related field.5+ years of relevant industry experience.Medical device industry experience is preferred.Requires strong organization...Medical deviceFull timeTemporary workWork visaFlexible hours- A renowned consulting firm is seeking a Quality Systems Specialist to manage customer complaints while ensuring compliance with FDA and ISO regulations. This role involves... ...experience in quality systems within the medical device or pharmaceutical industry. The position offers...Medical device
- ...on) global product transfers within the medical device industry 4. Able to communicate and... ...production lines. Job Description The Quality Engineering Project Manager provides leadership... ..., qualification, and risk-based compliance decisions across base business and development...Medical deviceWork at office
- ...evaluating severity, impact, risk, and compliance implications . Escalate issues to Exception... ...leaders, Business Process Owners, Quality, and other functions to ensure effective... ...years of regulatory, pharmaceutical, or medical device experience . Experience in Regulatory...Medical device
- Join to apply for the Quality Systems Specialist role at BioSpace... ...issues today and address the medical challenges of tomorrow. We strive... ...products, medical devices, combination products and biologics... ...shipment of final product are in compliance with Corporate and...Medical deviceTemporary work
$90k - $125k
...Location: LibertyvilleDepartment: Quality SummaryThe Sr. Design Assurance... ...of design controls in compliance with global regulatory requirements for medical devicesFacilitate project quality... ...13485 environment at a medical device manufacturerProject management training...Medical deviceWork at officeWorldwideVisa sponsorship- ...issues today and address the medical challenges of tomorrow. We strive... ...Description Responsible for quality of assigned products which... ...combination products, and medical devices to ensure business objectives... ...of product while assuring compliance to local, divisional, and...Medical deviceLocal areaWorldwide
- ...manufacturing by reviewing batch records and GMP documentation to ensure compliance with cGMP, Baxter policies, and local procedures. You will... ...for product release. Working closely with Manufacturing and Quality teams, you will handle documentation review processes,...Local area
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