Compliance Specialist
Randstad
Compliance SpecialistRandstad is seeking a Compliance Specialist for our global biopharmaceutical in Mettawa, IL. Location: Mettawa, IL 60045 Pay Rate: $42.00 – $44.00 per hour Contract Duration: 1 Year, possible extension Qualifications Must-haves: Education & Experience: High School Diploma or GED with at least 2 years of relevant professional experience. Technical Skills: Advanced MS Office proficiency (Outlook, PowerPoint, and Excel—including
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Compliance Specialist in Lake Forest, IL vacancy
- Job-ID29095910Reference26-23457Remote50% Remote Experience • 3-5+ years of experience in regulatory compliance, information security, and/or data privacy • Demonstrated experience working within cross-functional teams including Legal, IT, Security Operations, and...SuggestedRemote work
$42 - $44 per hour
Randstad is seeking a Compliance Specialist for our global biopharmaceutical in Mettawa, IL. Location: Mettawa, IL 60045 Pay Rate: $42.00 – $44.00 per hour Contract Duration: 1 Year, possible extension Qualifications Must-haves: Education...SuggestedHourly payPermanent employmentContract workTemporary workWork experience placementLocal areaHome officeShift work$30 - $35 per hour
...Description # Home # Search Jobs # Job Description Quality Assurance Compliance Specialist Contract: North chicago, Illinois, US Salary Range: 30.00 - 35.00 | Per Hour Job Code: 370942 End Date: 2026-09-06 Days Left: 17 days...SuggestedHourly payContract workTemporary work$68k - $136k
...providing lab results for millions of people. The Regulatory Affairs Specialist II is responsible for implementing and maintaining the... ...Understands, implements, and maintains the quality policy. Ensures compliance and is able to demonstrate knowledge of site and division...SuggestedWork experience placementWorldwide- ...are accurately documented and aligned across markets. Monitor submission and approval activities to maintain data integrity and compliance. Support audit and inspection requests related to regulatory submissions and approvals. Participate in monthly quality control reviews...SuggestedRemote work
- Position Title: Compliance Specialist Length of Contract: 1 year Location/Site: North Chicago, IL Minimal travel (less than 2 weeks per year)What are the top 3-5 skills, experience or education required for this position: Highly analytical with outstanding written and...Contract workWork experience placementRemote workHome office
- US Tech Solutions is seeking a Clinical Document Management Associate II for a 12-month contract with a hybrid work model (remote Mon, Fri; onsite Tue-Thu). The role focuses on keeping the Master File inspection-ready per ICH GCP, performing quality checks, and supporting...Remote jobContract work
- ...regulatory plans and assists in execution including creation and maintenance of global registration dossiers. Assures full regulatory compliance of all documentation for submissions and change management. Essential Duties & Responsibilities • Provides regulatory...Hourly pay
- ...Regulatory Affairs Specialist Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time...
- ...Hiring: Quality Assurance Compliance Specialist Location: North Chicago, IL 60085 Hybrid We are looking for an experienced QA professional to support pharmaceutical quality operations, lead quality projects, improve QA processes, and ensure compliance with company...For contractors
$40 per hour
...insurance. Job Description: Position is primarily responsible for collecting, organizing, and analyzing large sets of compliance data from multiple sources, identifying trends, and developing metrics and reporting for key stakeholders. Position will...Contract workWork experience placementWork at officeMonday to FridayShift work- Location: Mundelein, Illinois, United StatesCompany: MedlinePosted: 2026-08-19Medline in Mundelein, IL is seeking an Adverse Event Specialist to manage product complaint remediation and MDR reporting responsibilities. The role requires applying FDA 21 CFR 803 criteria...
- Senior International Trade Compliance SpecialistCorporate Headquarters12575 Uline Drive, Pleasant Prairie, WI 53158Interested in the global... ...materials! As a Senior International Trade Compliance Specialist, you’ll tackle regulatory hurdles, find tariff savings and bring...Full time
- ...control/change plan activities, and request/collection of feedback from manufacturing sites and affiliates. The person will ensure compliance to the quality system as it pertains to Supplier Change Notifications. Responsibilities: Monitor global Supplier Change...
- Position Title: QA Compliance Specialist II Work Location: 60064, North Chicago, IL Assignment Duration: 06 Months (Possible extension) Work Arrangement: Onsite (warehouse floor support required) Position Summary: Assure compliance with FDA current Good manufacturing Practices...
- 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...
- ...Network Security EngineerWe are seeking a dedicated professional to join our team to support ongoing risk, vulnerability, and compliance management activities. This role requires a blend of technical awareness, organizational coordination, and risk management responsibilities...
$61.3k - $122.7k
...executives, and scientists. The Opportunity The Regulatory Affairs Specialist II (Medical Events) position supports the Infectious Disease... ...the division’s products. You will be accountable for ensuring compliance with Medical Device Reporting regulations (including 21 CFR 80...Worldwide- ...Pharmaceutical Recruiter - Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device... ...Support execution of global regulatory strategies and ensure compliance for submissions and change management. Identify documentation...Contract work
$56k - $85k
Job Description The Trade Compliance Specialist works as an integral member of the Fortune Brands Innovations Customs team. This role will assist with the day-to-day operations for all Trade Compliance and Customs related activities for the company's global divisions located...Remote workMonday to FridayFlexible hours$56k - $85k
...transforming spaces into havens and strive to positively impact our business, shareholders, people and the planet. Job Title Trade Compliance Specialist Location Hybrid schedule: Deerfield HQ Tuesday‑Thursday, remote Monday & Friday. Responsibilities Assist in preparing and...Remote workMonday to FridayFlexible hours- Spectraforce Technologies in North Chicago, IL is seeking a QA Compliance Specialist II to ensure FDA cGMP and cGDP compliance, align with corporate policies, and guide operational processes and documentation. You will assess outages and deviations for compliance, serve...
- ...submission content deliverables such as cover letters and forms. Performs detailed quality reviews of published output to ensure compliance with Regulatory Standards and Health Authority guidances including verification of content, bookmarks, hypertext links and tables...Full timeTemporary workWork at officeLocal areaRemote work
- ...development compounds. The Associate Director will interface with International Marketing, Global Legal and Office of Ethics and Compliance with regard to advertising and promotion strategies and tactics intended for use globally. Responsibilities: Reviews and...Full timeWork at officeLocal area
- Company Description About AbbVie 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...Full timeWork at officeLocal area
- Katalyst CRO in Mundelein, Illinois, is seeking a candidate to support remediation activities under FDA requirements. This role involves reviewing historical complaint files, applying current FDA definitions, and preparing MDRs when necessary. The ideal candidate will have...
- ...and US registrations for medical devices. The role involves planning registration packages, liaising with agencies, and ensuring compliance across changes and submissions. Candidates should have strong regulatory expertise and cross-functional collaboration skills. The...
- AbbVie in North Chicago, IL seeks a Reconciliation Analyst to manage payment processes for consultant engagements, ensuring compliance and timely payments. You will review payment requests, coordinate with HCPs and business owners, procure POs, and support closeouts and...
- Medline Industries, LP in Mundelein, IL is seeking an Adverse Event Specialist to manage product complaint remediation and MDR reporting. You will review historical and new complaints to determine MDR reportability under FDA rules (21 CFR 803) and submit MDRs through the...
- 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...Temporary workWork at officeLocal areaRemote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Compliance Specialist. Be the first to apply!
Related searches
- research compliance officer Lake Forest, IL
- regulatory compliance associate Lake Forest, IL
- regulatory officer Lake Forest, IL
- healthcare compliance officer Lake Forest, IL
- medicare compliance specialist Lake Forest, IL
- regulatory affairs specialist Lake Forest, IL
- compliance specialist Lake Forest, IL
- compliance consultant Lake Forest, IL
- coding compliance specialist Lake Forest, IL
- aml compliance analyst Lake Forest, IL


