Regulatory Affairs Associate I
Randstad
Regulatory Career Opportunity
Ready to elevate your regulatory career? This opportunity allows you to take ownership of managing, compiling, and authoring CMC sections for marketed product variations, directly influencing global compliance and product lifecycles. Based out of a state-of-the-art facility in Lake County, this role offers a dynamic hybrid schedule balancing collaborative on-site teamwork with remote flexibility.
Vacancy posted 14 hours ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Associate I in Great Lakes, IL vacancy
- ...Responsibilities Support regional Regulatory Information Management (RIM) activities using systems such as COSMOS, HUBBLE, and CIU. Create... ...initiatives. Requirements Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related discipline. Experience...Suggested
- ...Regulatory Affairs Associate I Are you a recent life sciences graduate looking to launch your career with a Top-Tier Global Pharma Leader? This hybrid Regulatory Affairs Associate I role in North Chicago, IL, offers an incredible opportunity to gain hands-on experience...SuggestedContract work
$28 - $32.29 per hour
...Are you a recent life sciences graduate looking to launch your career with a Top-Tier Global Pharma Leader? This hybrid Regulatory Affairs Associate I role in North Chicago, IL, offers an incredible opportunity to gain hands-on experience in regulatory information management...SuggestedHourly payContract workTemporary workWork experience placement3 days per week- ...Job Title: Regulatory Affairs Associate. Location: Lake Forest, IL Duration: 12 Months Pay Rate: $33-$35 on W2 per hour. Position Summary Provides regulatory support and expertise associated with global and US electronic publishing and submission of...SuggestedHourly pay
- ...of planned submissions and approvals in a region to: Supports regulatory information management activities in the region focusing on... ...Correspondence/responses from agency are imported into Cosmos in association with relevant activity Response structures linked to relevant...SuggestedFull timeLocal area
- ...coordinate activities with all functional departments in support of regulatory filings. Responsibilities: Manage, compile, and... ...Preferred Experience: 1-2 years pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3)...Contract workShift work
- ...of planned submissions and approvals in a region to: Supports regulatory information management activities in the region focusing on... ...Correspondence/responses from agency are imported into Cosmos in association with relevant activity Response structures linked to relevant...Local area
- ...Regulatory Affairs Specialist Responsible 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...
$27 - $30 per hour
...Regulatory Affairs Associate I Onsite - Lake County - Hybrid (Tues, Wed, Thurs onsite) Length of assignment: 1 year 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- Senior Pharmaceutical Recruiter - Unicon Pharma Inc Regulatory Affairs Specialist Provide regulatory support for U.S. and global medical device... ...in medical devices (RAC preferred). Seniority level: Associate Employment type: Contract Job function: Analyst Industries...Contract work
- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software...
- ...distributor of shipping, industrial and packaging materials! As a Senior International Trade Compliance Specialist, you’ll tackle regulatory hurdles, find tariff savings and bring Uline’s high quality products to international destinations. Careers Packed with...
$55.64k - $92.73k
...along with administering the fiduciary account program. Essential Functions: Ensures compliance with all state and federal regulatory requirements including, but not limited to, Anti-Money Laundering, OFAC, BSA, GLBA, HMDA, Reg CC, Reg D, Reg E, Reg Z, Truth in...Local area$65.5k
...for the successful close-out of activities, ensuring financial, transparency and compliance accuracy of all costs and activity associated with events planned within AbbVie's Business Service Group or by Third Party Vendors, as required by country specific,...Temporary workWork experience placementLocal areaFlexible hours- ...Senior Pharmaceutical Recruiter. The ideal candidate will provide regulatory support for both U.S. and global medical device submissions,... ...'s degree and at least 2 years of experience in Regulatory Affairs within the medical device field are essential. #J-18808-Ljbffr...
- BioSpace in North Chicago is looking for a candidate to ensure GxP compliance with AbbVie policies and global regulations. The role requires managing compliance initiatives and working effectively within team environments. A Bachelor’s degree in a scientific field is required...
- A propane services company is seeking a Compliance Assurance Specialist in Gurnee, Illinois. The role involves managing permitting and licensing for propane sales while ensuring compliance with relevant codes. Candidates should possess intermediate to advanced skills in...
- ...NFPA and IFC code requirements as defined by the jurisdiction having authority Correcting any non-compliance notices cited by the regulatory agencies (5-10% of position) Researching codes and requirements for new territories, researching jurisdiction requirements for...
- AbbVie in North Chicago is seeking a Program Compliance Analyst to ensure compliance and data accuracy in monitoring activities. The role involves interacting with Healthcare Providers and ensuring adherence to company policies and regulations. The ideal candidate should...
- An established industry player is seeking a detail-oriented logistics coordinator to manage import/export processes. This role involves supporting internal customers with shipment coordination, ensuring compliance with U.S. regulations, and maintaining accurate documentation...
- ...please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Associate, Regulatory Affairs Submission Management, manages medium to high impact, moderately complex submission projects involving multiple cross-functional...Temporary workLocal area
$30 - $35 per hour
Data Analyst / Report Developer Lake Forest, IL Hybrid role (Onsite 3x/week) $30-$35 per hour ABOUT THE ROLE Join as a Data Analyst / Report Developer (Label Conversion) and play a key role in a large-scale label conversion and standardization initiative, impacting approximately...Hourly payInternship3 days per week$20 - $24 per hour
Pay : $20.00 - $24.00/HR based on experience! Duration : 1-year contract (potential to extend/convert based on performance/budget) Location : 100% onsite; M-F 8:30 AM - 5:00 PM Responsible for: Support internal customers in coordinating the inbound and outbound shipment...Contract work- 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...
- Synectics Inc. in North Chicago is looking for a professional to support regulatory information management activities. Responsibilities include managing product registrations and ensuring accurate tracking of approvals and submissions in central systems. The ideal candidate...
$96.5k
...efficiencies. Act as a trusted source for trade compliance insights by proactively tracking, interpreting, and communicating regulatory and legislative updates to GTC stakeholders-ensuring the organization stays ahead of potential impacts with timely and actionable...Temporary workLocal areaWorldwide- Data Analyst As a Data Analyst in our client’s Genomics Research Center’s Bioinformatics Engineering team, you will be responsible for developing and running workflows to standardize and load project datasets in a centralized environment. You will work closely with ...
$87.2k - $145.3k
Work Location Type: Hybrid Req Number 332205 About Grainger W.W. Grainger, Inc. is a leading broad line distributor with operations primarily in North America and Japan. At Grainger, We Keep the World Working® by serving more than 4.6 million customers worldwide...Full timeH1bLocal areaWorldwide- Data Analyst A 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
- Description: Uses appropriate tools to collect, correlate and analyze data for use in (1) improving team and individual quality and productivity, (2) aid in the optimization of current business practices and (3) understand the impact of changes, improvements, or ...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Associate I. Be the first to apply!
Related searches
- regulatory Great Lakes, IL
- regulatory affairs Great Lakes, IL
- compliance lead Great Lakes, IL
- regulatory compliance Great Lakes, IL
- regulatory affairs assistant Great Lakes, IL
- compliance team leader Great Lakes, IL
- compliance technician Great Lakes, IL
- regional compliance officer
- accounting compliance officer
- global compliance coordinator



