Regulatory affairs associate
$28 - $32.29 per hourRandstad
job summary: 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, working with advanced industry systems in a collaborative, fast-paced environment. Duration: 1-Year Contract Location: North Chicago, IL (Hybrid: Onsite Tuesday, Wednesday, Thursday) Interview Process: 1-2 sequential virtual panel interviews location: North Chicago, Illinois job type: Contract salary: $28.00 - 32.29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Support regional regulatory information management (RIM) activities, focusing on key data systems and processes. Partner with the central data management team to create market-specific RIM objects following strict data standards. Create and update product registrations to align with new approvals, renewals, indications, or pack changes. Track, record, and update regulatory commitments, obligations, submissions, and agency correspondences. Monitor tracking systems to ensure submission and approval dates are accurately recorded and archived. Collaborate on monthly quality control reports, identifying data gaps and supporting remediation activities. qualifications: Bachelor's degree in a related life science field (Pharmacy, Biology, Chemistry, Medical Technology, or Pharmacology) Recent graduate with a Pharmacy or Health Sciences background Strong oral and written communication skills Ability to work onsite in North Chicago, IL, 3 days per week (Tuesday-Thursday) #LI-AO1 skills: Regulatory Affairs Operations, Regulatory Submission Compliance Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on click.appcast.io. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.
- ...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
- ...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
- ...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
$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
- ...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...
$55.64k - $92.73k
...activities, 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- ...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 as...
$65.5k - $125.5k
...responsible 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, federal...Temporary workWork experience placementLocal areaFlexible hours- ...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...
- 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...
- 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...
- 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...
$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- 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...
- 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...
- 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$76.96k - $125.84k
Ann & Robert H. Lurie Children’s Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year...Hourly payFull timePart timeWork at officeFlexible hours- ...experience in compliance, risk, legal, or regulated environments ~ Strong analytical skills and the ability to distill complex regulatory material ~ Proven ability to manage multiple priorities independently ~ Excellent written and verbal communication skills ~...Full timeTemporary workWork at officeLocal areaRemote workFlexible hours
- ...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
- ...controls, supplier management, deviations, documentation, CAPA, audits, experience with supplier change notifications, searching vendors in SAP, Soltraqs/Trackwise experience. Experience in a Regulatory Pharmaceutical Industry. #LI-KH1 #J-18808-Ljbffr The Fountain Group
- Select Source International is seeking a Contract Coordinator in North Chicago, IL, for a 12-month contract with potential extensions. You will handle the creation, negotiation, and implementation of contracts for consulting and promotional services while ensuring compliance...Contract work
- ...over 4 years of experience in quality assurance and a Bachelor's Degree in a Science or Engineering field. Familiarity with SAP and Regulatory Pharma is essential. This role provides an opportunity to work within a dynamic team dedicated to quality management. #J-18808-...
$84.5k - $162k
...the department's long range plan. The role entails creating project plans, managing product launches, and ensuring compliance with regulatory agencies. The ideal candidate should have a Bachelor's degree in a related field, along with 5-10 years of relevant experience. A...- Bioinformatics Analyst We have an exciting contract opportunity for a Bioinformatics analyst within the Genomics Research Center to support a collaboration with the Ophthalmology, supporting drug discovery and basic disease biology investigations. The successful candidate...Contract work
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