Compliance Analyst
$40 per hourThe Fountain Group
Shift Information Monday-Friday, Standard Business Hours, Onsite Position! Pay range starts at $40+/hr! 12+ Month contract to start! This is a W2 Contract (No 1099/C2C), with a possibility of extension or conversion beyond the original duration based on performance & budget at that time. Our company offers our consultants a suite of benefits after a qualification period including health, vision, dental, life and disability insurance. Shift Information Monday-Friday, Standard Business Hours, Onsite Position! Pay range starts at $40+/hr! 12+ Month contract to start! This is a W2 Contract (No 1099/C2C), with a possibility of extension or conversion beyond the original duration based on performance & budget at that time. Our company offers our consultants a suite of benefits after a qualification period including health, vision, dental, life and disability 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 also be responsible for supporting day-to-day commercial compliance activities, identifying compliance concerns, developing communications and training, and assisting with audit preparation and remediation. Position will be in charge of managing multiple compliance workflows and projects while collaborating with commercial, legal, financial compliance, and ethics stakeholders to resolve issues and ensure compliance controls are followed. Qualifications Experience analyzing large sets of data with strong written and verbal communication skills is required! Advanced Microsoft Office skills including Excel with Pivot Tables, PowerPoint, Outlook, and SharePoint is required! Ability to manage multiple workflows simultaneously and coordinate actions with subject matter experts is required! Bachelor’s degree or equivalent professional work experience is required! 2+ years of pharmaceutical or related industry experience is preferred! Experience supporting compliance monitoring, audits, or commercial compliance activities is preferred! Who We Are The Fountain Group is a nationwide staffing firm based out of Tampa, FL 33607 with over 80 Fortune 100-500 clients. Since 2001, TFG has maintained a consistent standard of excellence, and our work is broadly recognized every year through numerous industry performance awards. Our success is a team effort. Browse our website tagged below for additional information on our company. We work in Life Sciences, Clinical, Engineering, IT, and more. Above all, we specialize in people. Please note: Candidates do not pay any fees to work with The Fountain Group. All staffing and placement services are provided at no cost to you —our clients cover all fees. #J-18808-Ljbffr
$68k - $136k
...and technical knowledge to a focused area of work assignments. Understands, implements, and maintains the quality policy. Ensures compliance and is able to demonstrate knowledge of site and division level policies and procedures.What You’ll Work OnVerifies with...SuggestedWork experience placementWorldwide- ...Device Reports (MDRs), including international vigilance reports for the division's products. You will be accountable for ensuring compliance with Medical Device Reporting regulations (including 21 CFR 803) and for the efficient and timely processing of potentially...SuggestedWorldwide
- ...Support execution of global regulatory strategies and ensure compliance for submissions and change management. Identify documentation... ...Seniority level: Associate Employment type: Contract Job function: Analyst Industries: Medical Equipment Manufacturing and Pharmaceutical...SuggestedContract work
- ...Industries, LP in 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 triage complaints, determine reportability under 21 CFR 803, and prepare submissions...Suggested
- ...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...SuggestedHourly pay
- Regulatory Affairs SpecialistResponsible 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 Reviews...
- ...Compliance Specialist 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 & Experience...Hourly payContract work
- ...Position Title: Compliance Analyst Length of Contract: 1 year (Potential Extension) Location/Site: North Chicago, IL (Hybrid module) Minimal travel (less than 2 weeks per year) What are the top 3-5 skills, experience or education required for this position: Highly analytical...Contract workWork experience placementRemote workHome office
$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...Hourly payPermanent employmentContract workTemporary workWork experience placementLocal areaHome officeShift work- ...A leading pharmaceutical company is seeking a Senior Analyst (Membership) to manage membership activities and contract eligibility... ...Illinois. The ideal candidate will analyze key data, support compliance efforts, and communicate vital market trends across teams. Requirements...Full timeContract work
- Abbott in Lake Forest, IL is seeking a Regulatory Affairs Specialist II to implement and maintain the quality system and support change control in manufacturing/operations. You will prepare U.S. regulatory submissions and coordinate with international affiliates to secure...
- Spectraforce Technologies in North Chicago, IL seeks a Compliance Analyst to support US Commercial compliance data analysis, reporting, and training development within ABS, Samples, and Peer to Peer Monitoring. The role requires strong analytical and communication skills...
- A leading healthcare firm in Lake Zurich, Illinois, seeks an experienced Analyst responsible for data analysis and compliance regarding membership and class of trade. The role requires 3-5 years of experience in contracting or healthcare and a Bachelor's Degree. Proficiency...
- ...of regulatory agency review. Work with region and country RA counterparts to evaluate changes for regulatory impact and to ensure compliance with applicable regulations. Accurately describes these changes for ease of regulatory agency review. Represents Global...Local area
$97.5k - $139.75k
...strategies 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 advice and support...Work at officeLocal area- ...registrations of medical device products. You will analyze regulatory requirements, create and maintain registration dossiers, and ensure compliance across submissions and change management. You will coordinate with regional teams, prepare agency meeting packages, and lead...
- ICU Medical is seeking an experienced Regulatory Affairs professional to support global and US registrations for device products. You will analyze requirements, create regulatory strategies, and maintain dossiers with oversight. Ideal candidates have 7+ years in medical...
- ...seeking an Adverse Event Specialist (Healthcare) to manage product complaints and MDR reporting. The role ensures FDA 21 CFR 803 compliance and leverages decision logic to determine reportability, coordinating with Quality, Regulatory Affairs, and R&D. The position requires...
- ...improvement of internal control reporting. The role involves maintaining control documentation, conducting testing, and ensuring compliance with regulations. Responsibilities include assisting audits and tracking remediation actions. Candidates should have 2-3 years of...Work at office
- ...determine MDR reportability under FDA rules. You will review historical and new complaints to ensure accurate reporting and full compliance with 21 CFR 803 and Quality System requirements. The role requires a bachelor's degree and 1+ year in a regulated environment, with...
- ...innovative products that improve the world. The Import/Export Analyst will be responsible for providing operational expertise to enhance... ...carriers to ensure satisfaction. The role will manage all imports and exports, ensure compliance with U.S. #J-18808-Ljbffr FLEX IncFlexible hours
- ...expertise for electro-mechanical device products. You will analyze requirements, prepare registration dossiers, ensure documentation compliance, and support regulatory strategy with cross-functional teams. You will liaise with regulatory agencies, evaluate manufacturing...
- 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...
- ...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...
- 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...
- ...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
- Job-ID29173168Reference26-24274Regulatory Information Management Contractor Location: Onsite - Hybrid (Tues, Wed, Thurs) - North Chicago Responsibilities May Include: Monitors activity in COSMOS (Regulatory Information Management solution) for assigned products and activities...For contractors
$87.2k - $145.3k
...in the United States now and for the foreseeable future will be considered for this position.Position DetailsThe Senior Reporting Analyst, Sourcing Extended Assortment serves as a lead analytics professional responsible for transforming complex data into actionable business...Full timeH1bLocal areaWorldwide- ...to determine severity, impact, and appropriate next steps. Escalate issue records to Exception Reports when needed based on risk, compliance impact, or process significance. Project manage Exception Reports in partnership with cross-functional stakeholders to identify...
- ...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...Remote work
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