Global Medical Devices Regulatory Affairs Associate
Unicon Pharma Inc
A leading pharmaceutical company located in Lake Forest, Illinois, is seeking a Senior Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions, focusing on compliance with FDA and EU requirements. Responsibilities include preparing registration packages, maintaining global regulatory dossiers, and collaborating across functions to resolve documentation issues. A Bachelor's degree and at least 2 years of experience in Regulatory Affairs within the medical device field are essential. #J-18808-Ljbffr Unicon Pharma Inc
- ...Pharmaceutical Recruiter – Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device submissions, including FDA and EU... ...devices (RAC preferred). Seniority level: Associate Employment type: Contract Job function: Analyst...Medical deviceContract work
- ...Job Title: Regulatory Affairs Associate. Location: Lake Forest, IL Duration: 12 Months Pay Rate: $33... ...regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding the structure of...Medical deviceHourly pay
- ...functional departments in support of regulatory filings. • Manage, compile... ...all levels and types of global personnel required •... ...including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD... ...for Class III implantable medical devices. May require an advanced...Medical deviceShift work
$29 - $32.29 per hour
...Summary Ready to elevate your regulatory career? This opportunity... ...variations, directly influencing global compliance and product... ...reports for Class III implantable medical devices. Coordinate cross-functional... ...specifically in Regulatory Affairs, R&D, or Manufacturing (...Medical deviceHourly payContract workRemote work- ...is part of Alcon's Quality & Regulatory Affairs function, ensuring products comply with global, local, and internal regulations... ...advantage. Support medical device and/or pharmaceutical products... ...directly related experience, associate’s degree with 16+ years, or master...Medical deviceLocal area
- ...Regulatory Affairs Specialist Responsible for filing necessary applications and handling all government interactions pertaining to... ...approval of manufacturing changes for Class III implantable medical devices. May require an advanced degree and 5-8 years of direct experience...Medical device
- Hobbsnews is seeking a Sr Regulatory Affairs Specialist to support the Medical Solutions Regulatory Affairs team. This role involves providing expertise for medical devices and managing projects for regulatory strategy, registrations, and compliance. The ideal candidate...Medical device
$113.3k - $226.7k
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000...Medical deviceWorldwide- ...and a minimum of 8 years of quality experience in pharma or medical device manufacturing. Key responsibilities include writing and maintaining... ...North Chicago, providing critical support to ensure compliance with corporate and regulatory standards. #J-18808-Ljbffr SPECTRAFORCEMedical device
$129.3k - $258.7k
Abbott is a global healthcare leader that helps people live more... ...products in diagnostics, medical devices, nutritionals and branded generic... ...the Medical & Scientific Affairs organization. We're empowering... ..., Clinical Development, Regulatory, Marketing, and Commercial teams...Medical deviceWorldwideShift work- ...Title: Regulatory Affairs Specialist Location: Mundelein, IL Duration: 3 to 6 Months Pay range... ...verification activities, and collaborating with global regulatory teams as needed to meet... ..., or regulatory affairs within the medical device or pharmaceutical industry Strong...Medical deviceTemporary work
$92k - $138k
...Senior Regulatory Specialist Under limited supervision... ...critical and complex global regulatory projects... ...regulatory strategies for new devices, new launch markets,... ..., etc.), engineering, medical technology, regulatory... ...in regulatory affairs in the medical device...Medical deviceMinimum wageWork experience placementLocal areaWorldwide- Position Global Marketing Lead Manager Location Vernon Hills, IL... ...0.00 Shift 1st Shift Client Medical Device Company Job Category... ...submissions background and Regulatory background dealing with claims... ...project execution (Medical Affairs, R&D, Quality and Regulatory...Medical deviceContract workShift workDay shift
$68k - $136k
Regulatory Affairs Specialist III Location: Buffalo Grove, IL (On-site). About the Role Support... ...regulatory and related teams. Develop global regulatory strategies for product development... .... 5 years’ experience in the medical device industry. 1-2 years of regulatory experience...Medical deviceShift work$66.5k - $88.02k
What Regulatory Affairs contributes to Cardinal Health Regulatory... ...pharmaceutical, medical and biotechnology companies... ...portfolio of medical devices. This could include... ...aligned with global medical device regulations... ...including documents associated with design inputs and...Medical deviceTemporary workWork experience placementWork at officeLocal areaImmediate startFlexible hours- ...find purpose and pride. What you'll be doing: The Associate General Counsel—Global Procurement & Real Estate will provide strategic day‑to... ...in‑house experience supporting a pharmaceutical and/or medical device company will be desirable. ~ Familiarity with AI...Medical deviceContract workTemporary workFlexible hours
- ...seeking an International Trade Compliance Specialist in Waukegan, IL. This role involves tackling regulatory hurdles and managing trade compliance programs while supporting the global economy. Candidates should hold a Bachelor’s degree and have strong communication and...
- ...Responsibilities: Support regional Regulatory Information Management (RIM) activities... ...and obligation tracking Partner with global and regional teams to ensure regulatory... ...Requirements: Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related...
- ...Regulatory Affairs Associate I Responsible for managing the activities for marketed product variations... ...~ Ability to work effectively with global cross-functional teams. ~ Familiarity... ...applicable eligibility requirements: medical insurance, dental insurance, vision...Temporary work
- ...Regulatory Career Opportunity Ready to elevate your regulatory career? This opportunity allows you to take ownership of managing, compiling... ...sections for marketed product variations, directly influencing global compliance and product lifecycles. Based out of a state-of-the-...Remote work
$27 - $30 per hour
...Regulatory Affairs Associate I Onsite - Lake County - Hybrid (Tues, Wed, Thurs onsite) Length of... ...Hourly Pay Rate: $27-30/hr (individual medical benefits available at a cost) Orion Group has partnered with a global pharmaceutical leader, seeking to hire...Hourly payWork at officeLocal areaWorldwide$176k - $242k
...Baxter Responsible for global strategic planning of the portfolio... ...for all aspects of regulatory strategy for the PSS hospital... ...function and represent Regulatory Affairs with business units and... ...experience in RA or related medical device function, including at least...Medical deviceTemporary workWork visaFlexible hours- AbbVie is seeking to enhance its Global Quality Organization by handling pharmaceutical, medical device, and combination product complaints. The role focuses on implementing and maintaining the Quality System, ensuring compliance with policies and regulations, and coordinating...Medical device
- ...and regulations. The ideal candidate should possess a BA/BS degree and have experience in data entry and financial practices, alongside strong interpersonal skills. Benefits include a comprehensive package with medical insurance and paid time off. #J-18808-Ljbffr AbbVie
- ...all functional departments in support of regulatory filings. Manage, compile, and author CMC... ...with all levels and types of global personnel required. Experience working with... ...experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3). Note...Contract workShift work
- ICU Medical in Lake Forest, Illinois, is seeking a Regulatory Affairs professional to provide expertise in the registration of medical devices. The role involves supporting the creation of global regulatory strategies, ensuring compliance, and acting as a liaison with regulatory...Medical device
- Katalyst CRO is seeking a professional for a Regulatory Affairs position located in North Chicago. Responsibilities include supporting regional Regulatory Information Management activities, maintaining regulatory records, and ensuring compliance across markets. The ideal...
$30 - $35 per hour
...July 27 ABOUT THE ROLE Our client is a global healthcare company dedicated to developing... ...and delivering innovative diagnostic, medical device, nutrition, and pharmaceutical... ...transportation High school diploma or GED required; Associate’s degree in Electronics, IT, Biomedical...Medical deviceWorldwide- ...Management processes across company's global network. This is a corporate-facing, non... ...processes, including pharmaceutical products, medical devices, cosmetics, combination products, and... ...to deliver strategic plans and regulatory updates. Provide support to specific areas...Medical deviceContract workMonday to Friday
$28.25 - $56.55 per hour
...Abbott is a global healthcare leader that helps people live more fully at all stages... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...Resources division. The Payroll Associate 2 is responsible for ensuring accurate...Medical deviceHourly payLocal area
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