-
Regulatory Affairs Associate
1 day ago
GForce Life Sciences Lake Forest, United StatesRegulatory Affairs Associate JR Lake Forest, IL · MUST BE ABLE TO WORK ON A W2 · Job Title: Regulatory Affairs Associate JR · Job Summary: · The Regulatory Affairs Associate Jr. supports the execution of External Regulations Standards and Guidance Documents packages by track ...
-
Regulatory Affairs Associate
1 week ago
GForce Life Sciences Lake Forest, United StatesRegulatory Affairs Associate – Abbott Park, IL · Must be able to work on a W2 · Job Summary: As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and ...
-
Regulatory Affairs Associate
1 week ago
Spectraforce Technologies Lake Forest, United StatesJob Title: Regulatory Affairs Associate · Location: Lake Forest, IL (Open for Remote) · Duration: 12 Months · Shift: 8 am - 5 pm · Duties:Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR). · Provides regulatory sup ...
-
Regulatory Affairs Associate
1 day ago
Planet Pharma North Chicago, United StatesAccountability / Scope: · As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. · Individual shall develop partnership with other regulatory ...
-
Regulatory Affairs Associate
2 days ago
Planet Pharma North Chicago, United StatesAccountability / Scope: · As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. · Individual shall develop partnership with other regulato ...
-
Regulatory Affairs Associate/IVDR
1 week ago
Intellectt Inc North Chicago, United StatesRole: Regulatory Affairs Associate · Location: Lake Forest, IL · Duration: 12 Months · Job description · candidate will be responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR)... Provides regulatory support for diagn ...
-
Regulatory Affairs Associate
2 days ago
PSG Global Solutions Chicago, United StatesWe're looking for a · Regulatory Affairs Associate , working in · Biotechnology/Medical Devices · industry in · 100 Abbott Park Road, Lake Forest, Illinois, 60064, United States . · Job description: · Responsible for filing necessary applications and handling all government ...
-
Regulatory Affairs Associate
2 days ago
INTELLECTT INC Chicago, United StatesRole: Regulatory Affairs Associate · Location: Abbott Park, Illinois · Duration: 8 Months on W2 · Job Description · Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental ...
-
AbbVie Lake Bluff, United StatesJob Description · Job DescriptionCompany 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 acr ...
-
Regulatory Affairs Associate
2 days ago
Planet Pharma Chicago, United StatesAccountability / Scope:As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. · Individual shall develop partnership with other regulatory f ...
-
Associate Dean of Academic Affairs
1 week ago
Chicago State University Chicago, IL, United StatesPosting Details · Position Information · Posting Number · S24042P · Posting Date · 11/09/2023 · Closing Date · 03/01/2024 · Title · Associate Dean of Academic Affairs · Working Title · Associate Dean of Academic Affairs · Salary Range · Employee Class · Administrator ...
-
AbbVie Mettawa, United States Full time· 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 ar ...
-
Jr. Regulatory Affairs Associate
2 days ago
INTELLECTT INC Chicago, United StatesRole: · Jr. Regulatory Affairs Associate · Location: · Lake Forest, IL only location's) · Duration: · 7 Months · Job Description · Manager regulatory submissions to ensure timely regulatory approval of medical devices. · Monitor changing regulations in geographies and tran ...
-
AbbVie Libertyville, United StatesCompany 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 area ...
-
AbbVie, Inc Mettawa, United StatesCompany 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 areas ...
-
AbbVie Mettawa, United StatesJob Description · Job DescriptionCompany 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 acr ...
-
USA - Regulatory Affairs Associate I
2 days ago
Pyramid Consulting Round Lake, United StatesImmediate need for a talented Regulatory Affairs Associate. This is a 06+ months Contract opportunity with long-term potential and is located in Round lake, IL (Onsite). Please review the job description below and contact me ASAP if you are interested. · Job ID: · Pay Range: $4 ...
-
Medical Devices- Associate Regulatory Affair
2 days ago
ULDQS, Inc. Schaumburg, United StatesJOB OBJECTIVES: · Assist RAM in managing the provision of certification services related to regulatory requirements in the medical device sector. Support the DQS RAM in respect to the MDSAP and ISO 13485 clients seeking certification via DQS MED Notified Body in Germany. Support ...
-
AbbVie Chicago, United States Full timeCompany 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 area ...
-
Tempus AI Chicago, United States Full timePassionate about precision medicine and advancing the healthcare industry? · Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evi ...
Regulatory Affairs Associate Jr - Lake Forest, United States - DivIHN Integration Inc
Description
DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent.
Visit us at
to learn more and view our open positions.Please apply or call one of us to learn more
For further inquiries regarding the following opportunity, please contact one of our Talent Specialists
Rashi at
Title: Regulatory Affairs Associate Jr
Location: Lake Forest, IL
Duration: 7 Months
Description
Exempt/Non Exempt: Non exemptYears.
Duties:
Manager regulatory submissions ot ensure timely regulatory approval of medical devices.
Monitor changing regulations in geographies and translate/communicate these requirements to project development and/or continuous improvement project teams.
Ensure all client product and procedures comply with applicable regulatory agency requirements and guidelines.
Manager is Insun Ho Start date will be determined when candidate is identified.
Supports execution of External Regulations Standards and Guidance Documents packages through tracking and monitoring ePAS packages from draft to final closure
Prepares metrics associated with the process for Executive Management Review (EMR)
Completes final signature approval of an ePAS package (i.e., FSG Approval)
Data review, analysis, and verification.
Education min. / Experience min.- BS in engineering or scientific degree / 1 years experience in a medical device or similarly regulated industry.
Top 5 skills/requirements -
Strong analytical and problem-solving skills.
Demonstrated competency and working knowledge of Excel, Word, PowerPoint, SharePoint, and Teams.
Communicate effectively verbally and in writing. Communicate with diverse audiences and personnel. Write and edit technical documents.
Ability to work with people from various disciplines and cultures.
Strong attention to detail.
Good organizational / project management skills to manage and track a wide range of tasks; ability to develop realistic action plans as well as prioritizing work activities.
Ability to schedule and organize multiple projects
What skillset will complimented - Similar skillset with a more regulatory or quality experience would be beneficial.
Interview: Initial interview via phone/video, 30 min. Then, select 2 or 3 candidates for an onsite interview
About us:
DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.
DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.