Regulatory Affairs Associate
Synectics
Description Uses knowledge of planned submissions and approvals in a region to: Supports regulatory information management activities in the region focusing on key systems and processes, including COSMOS, HUBBLE and CIU Connect with central data management team and following agreed upon data standards, proactively create market-specific RIM Objects. Create or Update product registration to align with approval or renewal (e.g. new registration, new validity date period, new indication, new pack) Commitment/Obligation recording and updating Bridge local regulatory processes with COSMOS activity framework to ensure accurate and complete tracking of all regulatory submissions and correspondences in the region, keeping alignment across countries and regions by liaising with other regional data leads to enabling accurate reporting Ensure submission dates, approval dates are recorded in Cosmos (structure and activity if first submission under the activity); may include follow-up with affiliate about distributor submission dates Monitor that submission has been archived via CIU Move activity to a completed status if a notification only activity Monitor that Correspondence/responses from agency are imported into Cosmos in association with relevant activity Response structures linked to relevant activity Approval letter imported in relation to relevant activity; Activity status and date updated to reflect approval Support Audit/Inspection requests in region related to submissions, commitments, correspondences and approval data in Cosmos Collaborate with central team for monthly QC reports, identify gaps and support data remediation activities. Capture requirements for relevant KPIs/metrics according to regional needs, and liaise with other regional data leads and Analytics team to develop advanced analytics capabilities in the Hubble Support adoption of system enhancements and new functionalities. Support migration and harmonization of data during system upgrades and process improvements. Qualifications Bachelor's degree in related life sciences (pharmacy, biology, chemistry, medical technology, pharmacology) Fresh graduate with pharmacy / health sciences background Good communication, both oral and written Benefits Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first of the month following at least 1 calendar year after employment begins. Synectics is an equal opportunity employer. #J-18808-Ljbffr
- ...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...SuggestedLocal area
- ...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
$40 - $50 per hour
...coordinate activities with all functional departments in support of regulatory filings. location: North Chicago, Illinois job type: Contract... ...pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3) #LI-AM1 skills: Project...SuggestedHourly payContract workTemporary workWork experience placementShift work- ...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:...SuggestedContract work
- ...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
- ...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...
- ...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...Hourly pay
- Planet Pharma in North Chicago, Illinois, is looking for individuals to support regulatory information management activities. The role involves using knowledge of regulatory submissions to ensure accurate tracking and reporting across regions. We welcome fresh graduates...
- ...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...
- ...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 materials is 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...
$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- 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...
$28 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...Hourly payContract workTemporary workWork experience placement3 days per week- ...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...
- 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...
$80.9k - $127.05k
...What Regulatory Affairs contributes to Cardinal Health Regulatory provides regulatory affairs and product development consulting services... ...affairs team. They are responsible for regulatory activities associated with convenience kitting (Presource® kitting). This includes...Temporary workWork experience placementWork at officeLocal areaFlexible hours- Bank of America is seeking a Financial Solutions Advisor Stage I in Lake Forest, Illinois, focused on enhancing clients' financial lives through tailored solutions. The role involves obtaining necessary licenses and engaging in client-facing activities within a financial...
- The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross‑functional regulatory submission teams. With input from the submission teams, this individual establishes and maintains submission content...Temporary work
- 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...
- BioSpace is looking for a qualified individual to ensure GxP compliance with AbbVie policies and global regulatory requirements. The role involves proactive evaluation of compliance needs and managing process improvements to enhance efficiency. Candidates should possess...
- Allergan is hiring an Associate in Regulatory Affairs Submission Management in North Chicago, IL. This role involves managing submission projects and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s Degree and at least 2 years of relevant...
$97.5k - $139.75k
Position Summary Provides regulatory support and expertise associated with global and US registration of medical deviceproducts, including in-depth analysis... ...agency review. Represents Global Regulatory Affairs at research and development meetings and presents agreed...Work at officeLocal area- BioSpace is seeking an Associate for Regulatory Affairs in North Chicago, Illinois. The role involves managing submission projects, ensuring timely and quality deliveries of submissions, and working with cross-functional teams. A Bachelor's degree and 2+ years in the pharmaceutical...
- ...distributor of shipping, industrial and packaging materials, and we’re growing! As an International Trade Compliance Specialist, tackle regulatory hurdles, find tariff savings and bring Uline’s high quality products to international destinations. Careers Packed with Potential...
- Planet Pharma Group is seeking a Regulatory Information Management professional in North Chicago, Illinois. The role involves supporting regulatory information management activities and ensuring accuracy in submissions and approvals. Qualified candidates should possess...
$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- ...cost 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
- 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...
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