Regulatory Affairs Specialist II: Diagnostics & Med Devices
Abbott
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 approvals. Ideal candidates have a technical Bachelor’s degree and at least five years of regulatory experience, with preferred background in medical devices or in-vitro diagnostics. #J-18808-Ljbffr Abbott
$68k - $136k
...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115... ..., providing lab results for millions of people. The Regulatory Affairs Specialist II is responsible for implementing and maintaining the...SuggestedWork experience placementWorldwideShift work$61.3k - $122.7k
...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 11... ...lab results for millions of people. The Regulatory Affairs Specialist II provides support for the regulatory department to...SuggestedFull timeWork experience placementWorldwideShift work- ...a global healthcare leader, seeks a Regulatory Affairs Specialist II (Medical Events) in Lake Forest, IL... ...You will review and submit Medical Device Reports (MDRs) and vigilance reports... ...procedures within a dynamic global diagnostics environment. #J-18808-Ljbffr RXinsider...Suggested
- ...ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations of medical device products. You will analyze regulatory requirements, create and maintain registration dossiers, and ensure compliance across submissions and change management...Suggested
- ICU Medical is seeking a Regulatory Affairs professional to support global 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...Suggested
$67.5k - $96.75k
...Position Summary Provides regulatory support and expertise associated with global and US... ...electronic publishing and submission of medical devices, including understanding the structure... ...Work with regional country Regulatory Affairs counterparts to evaluate and prepare...Full time- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring... ...design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and de...
- ...development and implementation of US and Canada regulatory strategic and tactical planning (RSTP)... ...Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others... ...or Canadadevice or combination product (device primary)experience preferred). US...
- 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
- ...Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA and... ...and at least 2 years of experience in Regulatory Affairs within the medical device field are essential. #J-...
$68k - $136k
...healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115... ...technology. The Opportunity We are recruiting for a Regulatory Affairs Specialist III to join our team on-site in Buffalo Grove, IL. We...WorldwideShift work- ...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...
- ...minimum of 8 years of quality experience in pharma or medical device manufacturing. Key responsibilities include writing and maintaining... ...in North Chicago, providing critical support to ensure compliance with corporate and regulatory standards. #J-18808-Ljbffr SPECTRAFORCE
$34.32 - $53.94 per hour
...finest in quality, innovative diagnostic equipment and information... ...for a Laboratory Specialist II. The Laboratory Specialist... ...instruments and products in the Regulatory and Clinical Affairs (RACA) Laboratory. In... ...and/or screening devices and confirmatory tests....Hourly payTemporary workWork at officeWorldwideShift work- Sysmex Corporation in Lincolnshire, IL, seeks a Laboratory Specialist II to support in‑house studies on Sysmex instruments and similar instruments within the Regulatory and Clinical Affairs (RACA) Laboratory. The role includes maintenance and QC of lab equipment and collaboration...Work at office
$70 - $74 per hour
...Job Title: Program Manager II (Content Operations Program Consultant) Location: Mettawa, IL 60045 Hybrid; M/F Remote - T/W/TH Onsite Contract: 1 year (Possible Extension) Pay Range: $70-74/hr What are the top 3-5 skills, experience or education required for...Contract workRemote work$129.3k - $258.7k
...with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...scientists.SENIOR MANAGER, Diagnostics PUBLIC AFFAIRS, Abbott (PUBLIC RELATIONS)LOCATION:... ...with various stakeholders including regulatory affairs, operations, quality, R&D, HR...$40 per hour
job summary: Are you ready to take the next step in your regulatory career with a global healthcare technology leader dedicated to advancing patient care through cutting-edge medical devices? In this role, you will play a key part in coordinating global submissions and...Hourly payContract workTemporary workWork experience placementRemote work- ...persistence to understand both big picture and accurate details as related to compliance. · Prior pharma experience a plus Job Title: Specialist Commercial Compliance PURPOSE: The Specialist, Commercial Compliance will meaningfully contribute to the US Commercial Compliance...Work experience placementRemote workHome office
- ...Finding a Full-Time job that fits your lifestyle isn't always easy. That's where Kelly comes in. We're seeking a Project Manager II / Senior Project Manager (Ad Agency)to work at a premier client in Mettawa, Illinois - 60045 . Pay rate and Shift Job Duration...Full timeTemporary workLocal areaRemote workShift workDay shift
- ...coordination of global teams across R&D, engineering, manufacturing, and regulatory to ensure robust supply and quality while minimizing costs.... ...candidate will have 10+ years in medical products or devices, strong MS Project skills, and experience driving cross-functional...
- ...applies project management expertise to lead complex programs to ensure delivery of safe and effective combination products and medical devices, on time and within budget. The Sr. PM partners with globally located, cross-functional teams, including external vendors, to drive...Full timeLocal area
- ...Senior Pharmaceutical Recruiter – Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU requirements. Prepare and organize registration packages and maintain global regulatory dossiers...Contract work
- Data AnalystA data analyst's main responsibilities include collecting, processing, and analyzing large datasets to extract meaningful insights. They create reports, use statistical methods to identify trends and communicate findings to help organizations make informed ...Work experience placementLocal area
- ...controls, supplier management, deviations, documentation, CAPA, audits, experience with supplier change notifications, searching vendors in SAP, Soltraqs/Trackwise experience. Experience in a Regulatory Pharmaceutical Industry. #LI-KH1 #J-18808-Ljbffr The Fountain Group
- ...@abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager, Regulatory Affairs US & Canada Strategy Lead – Aesthetics Device is responsible for the development and implementation of US and Canada regulatory strategic and tactical...Local area
- ...pharmaceutical company in North Chicago is seeking a Quality Assurance Specialist to monitor Supplier Change Notifications and ensure compliance... ...in a Science or Engineering field. Familiarity with SAP and Regulatory Pharma is essential. This role provides an opportunity to work...
$41 per hour
...I am a Recruiter with The Fountain Group. We are a national staffing firm and are currently seeking a Financial Analyst II A for a prominent client of ours. This position is located in North Chicago, IL . Details for the position are as follows: Pay Rate : $41...Hourly payContract workFlexible hours$78k - $156k
...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000... ...a source of information on the IT Compliance needs and regulatory environment.What You’ll Work OnLeads the IT Compliance...WorldwideShift work$149.3k - $298.7k
...of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,00... ...scientists. THE OPPORTUNITY: The function of a Director, Regulatory Affairs is to combine scientific, regulatory, and business...Worldwide
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