Regulatory Affairs Specialist II — Medical Devices
Abbott Laboratories
Abbott Laboratories in Lake Forest, IL seeks a Regulatory Affairs Specialist II to implement and maintain the quality system, support change control, and provide regulatory direction for team activities. The role includes preparing U.S. regulatory submissions and coordinating with international affiliates and agencies. Qualifications include a technical degree and at least 5 years of regulatory experience, with preference for medical devices familiarity and RAPS certification. #J-18808-Ljbffr Abbott Laboratories
$68k - $136k
## Regulatory Affairs Specialist IIApplylocations: United States - Illinois - Lake Foresttime type: Full... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...**Regulatory Affairs** **Specialist II****Working at Abbott** At Abbott,...Medical deviceWork experience placementWorldwideShift work- ...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...Medical device
- ...issues today and address the medical challenges of tomorrow. We... ...Description The Reporting Specialist II is responsible for executing... ...in-country teams, and the device quality assurance team to ensure... ...with pharmacovigilance, regulatory affairs, in-country teams, and...Medical deviceTemporary workWork experience placementWork at officeLocal area
$25 - $50 per hour
...businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines... .... The HVAC/Refrigeration Technician II provides 24/7 skilled-trade maintenance... ...and reclamation in compliance with regulatory requirements. Inspect, adjust, and repair...Medical deviceHourly pay- ...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...Medical deviceContract work
- ...Title: Engineer II, Packaging Location: Vernon Hills, IL Contract Term: 6+ Months Weekly 40.00 hours Description... ...experience candidates only. Job Description Summary Medical Device packaging engineer with knowledge and experience in regulated...Medical deviceContract workTemporary workFor contractorsFlexible hours
$97.5k - $139.75k
...Position Summary Provides regulatory support and expertise associated with global and US registration of medical device products, including in-depth analysis of the requirements... ...agency review. Represents Global Regulatory Affairs at research and development meetings and...Medical deviceWork at officeLocal area$80.9k - $127.05k
...What Regulatory Affairs contributes to Cardinal Health Regulatory provides... ...services to enable pharmaceutical, medical and biotechnology companies... ...Regulatory Affairs Specialist will support the Medical Solutions... ...regulations for medical devices and advise on impact of such...Medical deviceTemporary workWork experience placementWork at officeLocal areaFlexible hours- ...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-...Medical device
- ...seeking a detail-oriented, experienced Regulatory Affairs Consultant to join our team on a... ...regulations, ISO 13485, and international medical device requirements Reviewing labeling, IFUs... ...experience with both Class I and Class II medical devices Strong working knowledge...Medical deviceContract workRemote work
- A legal services firm is seeking a Compliance Officer II to oversee compliance functions and lead projects. This role involves mentoring junior colleagues, conducting risk assessments, and enhancing the organization's compliance program. Candidates should have a Bachelor...Full timeRemote work
- ...Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other...Medical deviceFor contractorsWeekend work
- ...encounters and must have a thorough knowledge of all of the regulations regarding eligibility/entitlement for home medical equipment and prosthetic devices, as well as programs such as Automobile Adaptive Equipment, Home Oxygen, Clothing Allowance, and Home Improvement...Medical device
- ...A medical device engineering company in North Chicago is seeking a mechanical/device engineer with extensive experience in drug delivery and device design. The candidate will be responsible for 3-D CAD design, MoldFlow analysis, and testing of prototypes in compliance...Medical device
- • Develops regulatory strategies for development projects, design changes and manufacturing improvements... .... Requirements A minimum of seven years of medical device industry experience with a minimum of five years in regulatory affairs with direct experience and authoring 510(k)...Medical device
$35 per hour
...Job Description Job Description Job Title: Medical Device Quality and Compliance Specialist Job Description We are seeking a Medical Device... ...based documentation. Collaborate with Quality, Regulatory Affairs, Clinical, R&D, Operations, and business stakeholders...Medical deviceContract workTemporary work- ...pharmacy which includes the preparation, dispensing, and delivery of medications as well as the provision of pharmaceutical care to patients... ...training for staff Disinfect and clean returned medical devices. Processes medical device returns and conducts functional...Medical deviceLocal area
- ...Diagnostic (CDx) program and will interact directly with external partners. ~ Minimum 5 years In medical/biotech industries. Knowledge of regulations and standards of medical devices. ~5-10 plus years of service industry experience with companies engaged in the...Medical device
$100 - $142 per hour
...Description: Overview: Engages and supports in medical device research that will eventually lead to the marketing of new products... ...the spread of disease to other animals. Supports the regulatory submission of products to the FDA for the various required...Medical deviceHourly payPart timeFor contractorsRelocation10 hours per week- ...packaging systems for sterile and non-sterile medical devices. The role involves working with cross-... ...teams (R&D, Quality, Manufacturing, Regulatory, Supply Chain) to ensure packaging meets... ...ISO 11607 experience Knowledge of Class II and/or Class III Medical Device regulations...Medical device
- ...and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies. Sotera Health goes to market through its three best-in-class businesses...Medical deviceWorldwide
$24 - $28 per hour
...developments in field(s) of expertise, regulatory requirements, a general knowledge of... .... ITIL certifications are considered. Medical device or healthcare experience is preferred.... ...IL . Incident Management & Operations Specialist Lead We’re unlocking community knowledge...Medical deviceContract workWork experience placementRemote work$153.71k - $157.5k
...serious health issues today and address the medical challenges of tomorrow. We strive to... ...EU Clinical Trial Regulation, EU Medical Device Regulation, EU In‑vitro Device... ...sponsors & managing communications with the regulatory authorities to successfully make public...Medical deviceTemporary workWork experience placement- ...-market supplier changes 4. Knowledge with applicable global regulatory requirements and industry standards (MDR requirements, ISO 13... ...organization including external vendors Reason: The Combination and Medical Device Products Consumable Device US team is expanding their support...Medical deviceWork at officeWork from home1 day per week
- ...management. Job Description Purchasing Specialist Location: Lake Forest, IL Duration: 3 months... ...with client Pharmaceutical and Device R&D organizations with procurement and outsourcing... .... Life Sciences, Pharmaceutical or Medical Device industry experience required. Previous...Medical deviceContract workWork at office
$90k - $100k
...enhancements Qualifications: Experience selling automation equipment, custom machinery, or engineered systems Pharmaceutical, medical device, or life sciences industry experience preferred Strong understanding of manufacturing and assembly automation processes...Medical device$17.5 - $20.5 per hour
...Operators to join our team for our esteemed client in Wheeling, IL. This is an excellent opportunity to contribute to a leading medical device manufacturing company while building valuable skills and enjoying competitive pay and benefits. About the Role: As a...Medical deviceHourly payWeekly payTemporary workLocal areaImmediate startFlexible hoursShift workRotating shiftDay shiftAfternoon shift- ...its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan,... ...management skills. Additional Information Looking for candidates with a background in the medical device industry. #J-18808-Ljbffr...Medical device
- ...manufacturing processes, including pharmaceutical products, medical devices, cosmetics, combination products, and biologics. This role is... ...into tactical objectives to deliver strategic plans and regulatory updates. Provide support to specific areas as needed, such as...Medical deviceContract workMonday to Friday
- ...Job Description Job Description Our client is a wellestablished and growing contract manufacturer serving the Aerospace and Medical Device industries. They are hiring a CMM Programmer responsible for developing and writing CMM programs to inspect highprecision...Medical deviceFull timeContract workTemporary work
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