GMP Documentation & Quality Compliance Specialist
Baxter International Inc.
Baxter International Inc. is seeking a Documentation Specialist to support manufacturing by reviewing batch records and GMP documentation to ensure compliance with cGMP, Baxter policies, and local procedures. You will help maintain the integrity of manufacturing records, ensuring they are complete, accurate, and ready for product release. Working closely with Manufacturing and Quality teams, you will handle documentation review processes, investigations, and document control activities to #J-18808-Ljbffr Baxter International Inc.
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the GMP Documentation & Quality Compliance Specialist in Round Lake, IL vacancy
$30 - $35 per hour
...Home # Search Jobs # Job Description Quality Assurance Compliance Specialist Contract: North chicago, Illinois, US Salary Range... ...management. Maintain and manage the validation document library to ensure compliance with quality standards....SuggestedHourly payContract workTemporary workCollabera
North Chicago, IL1 day ago- ...candidate is responsible for providing quality assurance support for some or all parts... ...and affiliates. The person will ensure compliance to the quality system as it pertains to... ...controls, supplier management, deviations, documentation, CAPA, audits, experience with supplier...Suggested
- Amcor Flexibles, LLC is seeking a quality/specification professional to support specification reviews and quality systems compliance. You will collaborate with the Product Data... ...efforts. A strong eye for detail and solid documentation practices are essential. #J-18808-...Suggested
$88k - $121k
...from one day to the next. As a Quality Associate II, you are... ...You will independently manage compliance audit processes and serve as... ...including back room management, document retrieval, and commitment tracking... ...of risk. Expertise in GMP regulations and regulatory inspection...SuggestedOdd jobTemporary workWorldwideWork visaFlexible hoursBaxter International Inc
Round Lake, IL23 days ago- ...6-08-17Baxter International Inc. seeks a Quality Associate II within the Quality organization... ...audit quality systems and regulatory compliance. You will manage internal audits, CAPA, inspections... ...improvement.The role emphasizes GMP knowledge, strong analytical skills, and...SuggestedWorldwide
$22 per hour
A talent acquisition firm is seeking a Quality Document Technician for a 6-month contract in Round Lake, IL. The role includes responsibilities like creating and distributing quality documentation, maintaining equipment, and identifying process improvements. Ideal candidates...Contract workFlexible hours$88k - $121k
...the same from one day to the next. As a Quality Associate II, you are unafraid of... ...changes for regulatory, product quality, and compliance impact; coordinate cross-functional... ...work instructions, and quality system documentation to ensure compliance with regulatory requirements...Odd jobTemporary workWork at officeWorldwideWork visaFlexible hoursBaxter
Round Lake, IL1 day ago$96k - $132k
...purpose and pride. Your Role at Baxter As a Quality Associate III, you are unafraid of... ...inspection readiness and regulatory compliance. Will also lead complex quality investigations... ...product, process, equipment, supplier, documentation, and quality system changes for...Temporary workWork visaFlexible hours- ...evaluating severity, impact, risk, and compliance implications . Escalate issues to Exception... ...leaders, Business Process Owners, Quality, and other functions to ensure effective... ...external audits and inspections , including documentation coordination, issue follow-up, and...
K3-Innovations Inc
North Chicago, IL9 hours ago - Join to apply for the Quality Systems Specialist role at BioSpace Company Description... ...of support may include the Document Center, Device QA, Labeling... ...of final product are in compliance with Corporate and... ...Knowledge of QA systems and GMP compliance requirements including...Temporary work
- Nemera is seeking a quality inspector to support the Quality Lead and Operational Quality Manager in achieving product quality and process efficiency. You will read drawings, perform measurements, document results, and communicate corrective actions across teams. The role...Hourly payShift work
- A leading pharmaceutical company in North Chicago is seeking a Quality Assurance Specialist to monitor Supplier Change Notifications and ensure compliance with quality systems. The ideal candidate should have over 4 years of experience in quality assurance and a Bachelor...
$104k - $143k
...role at BaxterAs a Principal Specialist, Global Regulatory Affairs,... ...maintain market access and compliance throughout the product lifecycle... ...Regulatory Affairs, R&D, Quality, Marketing, and Operations,... ....Maintain EU MDR regulatory documentation and support updates to technical...Full timeTemporary workWork visaFlexible hours- ...records and work cross-functionally with Quality, Regulatory, Operations, and other... ...identifies reportable events. Support compliance with FDA Quality System Regulations, including... .... Experience managing high volume documentation reviews or participating in large-scale...
Katalyst HealthCares & Life Sciences
Mundelein, IL2 days ago - ...Biorational Company in Libertyville, IL, seeks an experienced Trade Compliance Specialist to maintain and advance the global trade compliance program. The role coordinates import/export documentation, tariff classification, and regulatory reporting, partnering with logistics...
Valent USA
Libertyville, IL8 hours ago - Baxter International Inc. is seeking a Quality Associate III to manage senior-level QMS processes and drive timely, compliant investigations. You will partner with Manufacturing, Regulatory Affairs, and other teams to ensure inspection readiness and data integrity while...
$104k - $143k
...at Baxter As a Principal Specialist, Global Regulatory Affairs,... ...maintain market access and compliance throughout the product lifecycle... ...Regulatory Affairs, R&D, Quality, Marketing, and Operations,... ...Maintain EU MDR regulatory documentation and support updates to technical...Temporary workWork visaFlexible hoursBaxter International Inc
Round Lake, IL13 days ago- ...reputable law firm in Vernon Hills is seeking a Controls Specialist to support the execution and improvement of... ...reporting. The role involves maintaining control documentation, conducting testing, and ensuring compliance with regulations. Responsibilities include assisting...Work at office
$66 - $72 per hour
...Exception Reports when warranted by risk, compliance impact, or process significance.... ...Affairs leaders, Business Process Owners, Quality, and other functional partners to ensure... ...and inspections, including coordinating documentation, tracking issues, and supporting timely...Contract workTemporary workWork at officeRemote work$40 per hour
...Job Description Job Description Job Title: Senior Quality Assurance Specialist | Pharmaceuticals Location: North Chicago, IL Hire... ...Strong understanding of pharmaceutical Quality Systems and compliance requirements. Communication: Excellent verbal and written...Long term contractFor contractorsRemote workMonday to FridaySterling Engineering Inc.
North Chicago, IL2 days ago$64.7k - $80.9k
...OVERVIEW Role will support Specification Review and Quality Systems according to standards to make sure plant is in compliance and then assist with improvement projects... ...customer specifications and other associated documents to ensure all relevant data is captured and recorded...Full timeTemporary workWork at officeRemote workWorldwideFlexible hours- ...Exception Reports when needed based on risk, compliance impact, or process significance.... ...Affairs leaders, Business Process Owners, Quality, and other functions to ensure issue... ...inspections, including coordination of documentation, issue follow-up, and response support...
- ...submissions and correspondence are accurately documented and aligned across markets. Monitor... ...to maintain data integrity and compliance. Support audit and inspection requests related... ...submissions and approvals. Participate in monthly quality control reviews, identify data gaps, and...Remote work
- ...Promotion safeguards products and practices to adhere to the highest quality and regulatory standards. The Associate Director will design... ...Marketing, Global Legal and Office of Ethics and Compliance with regard to advertising and promotion strategies and tactics...Full timeWork at officeLocal area
AbbVie Inc.
Mettawa, ILmore than 2 months ago - ...Baxter Healthcare is seeking a Principal Specialist, Global Regulatory Affairs to lead... ...submissions that maintain market access and compliance throughout the product lifecycle. You will... ...with Regulatory Affairs, R&D, Quality, Marketing, and Operations, guiding submissions...
Baxter Healthcare Corporation
Round Lake, IL3 days ago - ...-518-4376. Bilingual Preferred The QA Specialist is responsible for conducting on-site client... ...councils and committees Insurance compliance with rules and regulations... ...improvements to policies, procedures, and documentation Maintains compliance with federal and...Full timeWork at officeLocal areaFlexible hours
- ...Baxter is seeking a Principal Specialist, Global Regulatory Affairs to lead regulatory activities... ...support submissions to maintain market access and compliance throughout the lifecycle. Working with Regulatory Affairs, R&D, Quality, Marketing, and Operations, you will guide...
Baxter
Round Lake Beach, IL3 days ago - ...Mundelein, IL is seeking an Adverse Event Specialist responsible for product complaint remediation and MDR reporting in compliance with FDA requirements. You will review and... ...submissions via eMDR, while coordinating with Quality, Regulatory Affairs, and R&D to gather...
Medline Industries
Mundelein, IL1 day ago - 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 continuous improvement in product quality and customer satisfaction. Ideal candidates have a bachelor...
- ...projects to ensure the timely delivery of high-quality dossiers that meet technical... ...quality reviews of published output to ensure compliance with Regulatory Standards and Health... ...implementation of internal process and standards documents relating to publishing and publishing...Full timeTemporary workWork at officeLocal areaRemote work
AbbVie
North Chicago, IL10 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to GMP Documentation & Quality Compliance Specialist. Be the first to apply!
Related searches
- quality manufacturing Round Lake, IL
- quality equipment Round Lake, IL
- supplier quality Round Lake, IL
- quality tech Round Lake, IL
- quality Round Lake, IL
- air quality Round Lake, IL
- quality inspection Round Lake, IL
- quality distribution Round Lake, IL
- compliance technician Round Lake, IL
- compliance team leader Round Lake, IL