Regulatory Affairs Associate II
Randstad
Regulatory Affairs Associate II
Advance your regulatory career in North Chicago with a top-tier global pharmaceutical leader. We are seeking a detail-oriented Regulatory Affairs Associate II to manage, compile, and author Chemistry, Manufacturing, and Controls (CMC) submission sections for marketed product variations. In this hybrid role, you will collaborate with cross-functional teams to ensure timely and compliant regulatory filings. Location: North Chicago, Illinois
$29 - $33 per hour
...Regulatory Affairs Associate II - CMC Module 3 and Marketed Product Variations Location: Lake County, IL | Hybrid Length of Assignment: 6 months initially Pay Rate: $29-33/hr (medical benefits available at a cost) Job Description: The Regulatory Affairs Associate...SuggestedWork at officeWorldwide$40 - $43 per hour
...Regulatory Affairs Associate II The Regulatory Affairs Associate II plays a key role in bringing medical device products to patients by preparing and managing regulatory submissions and leading interactions with regulatory agencies. This role partners closely with internal...SuggestedContract workTemporary workWork at officeRemote work- ...Regulatory Affairs Associate IIAdvance your career as a Regulatory Affairs Associate II with a top-tier global pharma leader in North Chicago, IL. This hybrid role offers an exciting opportunity to work directly with internal and external partners to deliver life-changing...Suggested
$40 - $43 per hour
Job Title: Regulatory Affairs Associate II Job Description Responsibilities Prepare regulatory submissions, including new applications, amendments, renewals, annual reports, supplements, and variations under limited supervision, and respond to regulatory information requests...SuggestedContract workTemporary workWork at officeRemote work$30 - $34.57 per hour
job summary: Advance your regulatory career in North Chicago with a top-tier global pharmaceutical leader. We are seeking a detail-oriented Regulatory Affairs Associate II to manage, compile, and author Chemistry, Manufacturing, and Controls (CMC) submission sections...SuggestedHourly payContract workTemporary workWork experience placement- ...Maintains awareness of and utilizes current best practices for use of regulatory business systems within the group.Individual is responsible... ...pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3)Responsible for filing...Shift 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
$62 - $67 per hour
...Project Manager II - Department Reorganization / Organizational Transformation Location: Mettawa, IL Schedule: Hybrid - Tuesday, Wednesday & Thursday onsite; Monday & Friday remote Contract: 6 months to start, with potential for extension Pay: $62- $6...Contract workWork at officeRemote workWorldwideMonday to Friday- Wipfli is seeking a Regulatory Compliance Consultant II to work in person, remote, or hybrid in the Chicago, IL area, with about 20% travel. The role focuses on risk assessment, remediation, testing, and reporting for financial institutions, supporting governance and management...Remote job
- Job-ID32908843Reference26-01550 Summary: The Manager, Process Excellence within Regulatory Affairs is responsible for managing key process excellence and issue management activities that support compliant, efficient, and inspection-ready Regulatory Affairs operations....
- ...Reference26-00999Remote50% Remote Responsibilities: Support regional Regulatory Information Management (RIM) activities using systems such as... ...initiatives. Requirements: Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related discipline Experience...Remote work
- Job Title: Specialist Commercial Compliance PURPOSE: The Specialist, Commercial Compliance will meaningfully contribute to the US Commercial Compliance team with data analysis, communication and coaching, metrics reporting, and execution of the day-to-day operations for...Work experience placementRemote workHome office
- 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
- ...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...
- ...Regulatory Affairs AssociateLocation: Lake Forest, ILDuration: 12 MonthsPay Rate: $33-$35 on W2 per hour.Position SummaryProvides regulatory support and expertise associated with global and US electronic publishing and submission of medical devices, including understanding...Hourly pay
- ...cross-functional project management Preferred Experience ~6 years pharmaceutical experience including 5 years in regulatory affairs or 5 years in Discovery, R&D, or Manufacturing ~ Experience working in a complex and matrix environment ~ Strong oral...For contractors
- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring... ..., and sales of medical devices (including Class I and II devices, software as a medical device, and de novo devices)...
$41 per hour
...I am a Recruiter with The Fountain Group. We are a national staffing firm and are currently seeking a Financial Analyst II A for a prominent client of ours. This position is located in North Chicago, IL . Details for the position are as follows: Pay Rate : $41...Hourly payContract workFlexible hours$22 - $28 per hour
...national staffing firm and we are currently seeking a Sales Analyst II for a prominent client of ours. This position is in Lake... ...improvements related to identifying the appropriate contract type and associated fee, then implement said solutions. ~ Collaborates with the...Contract work$100k - $110k
...Permanent, Project Manager II, Combination Products Summary Our client, a small medical device development company, has engaged... ...active testing programs ~ Working knowledge of applicable regulatory and quality system requirements including cGMP, cGLP, cGDP, ISO...Permanent employmentFull timeImmediate start- Job-ID29074176Reference26-23042Remote50% RemoteWhat are the top 3-5 skills, experience or education required for this position: Program Mgmt Operations mgmt. Process mgmt. Content operation Suggested Title: Content Operations Program Consultant Job Description The Content...
- ...AbbVie seeks a Scientist II Outsourcing Specialist to serve as the primary liaison between internal development teams and external service providers. The role coordinates global outsourcing activities for early-phase pharmaceutical development, managing timelines, budgets...Contract workShift work
- North South Consulting Group is seeking a part-time Personnel Assistant II (Identity Credentialing Specialist) to provide professional customer service and administrative support in a secure credentialing environment. You will verify identities, process credential applications...Part time
- ...We are currently seeking a detail-oriented, experienced Regulatory Affairs Consultant to join our team on a contract basis. The opportunity is... ...industry Demonstrated experience with both Class I and Class II medical devices Strong working knowledge of FDA submissions (including...Contract workRemote work
$55.64k - $92.73k
...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 Savings...Local area- Technical Project Manager II The project manager will lead technology projects from conception to execution, including gathering of business and system requirements, management of software design and development activities including: the development and maintenance...
- Applitrack is seeking a School Resource Officer II for the Northbrook Admin Offices to ensure a safe and secure school environment. Responsibilities include assisting administration, coordinating with law enforcement, and educating students on safety and law enforcement...
$66k - $89k
...home, Wipfli offers a career-defining opportunity. The Regulatory Compliance Consultant II can work in person, remote, or in a hybrid environment... ...potential solutions to identifying regulatory gaps and associated risks Present information in a concise and effective manner...Temporary workLocal areaRemote workFlexible hours- ...Abbott seeks a Regulatory Affairs Specialist for the Transfusion Medicine Business in Abbott Park, Illinois. This role supports regulatory activities for medical device product development, market entry, and compliance across US and international markets. Responsibilities...
$58.24k - $70.72k
...you reach your full potential. Job Description The Analyst II, Chemistry Laboratory evaluates the chemical and physical... ...procedures Performs other duties as assigned Qualifications ~ Associate Degree in Chemistry or similar discipline ~5+ years of laboratory...Hourly payFull timeImmediate start
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Associate II. Be the first to apply!
- regulatory Great Lakes, IL
- regulatory affairs assistant Great Lakes, IL
- regulatory compliance Great Lakes, IL
- compliance technician Great Lakes, IL
- compliance Great Lakes, IL
- regulatory affairs Great Lakes, IL
- temporary compliance analyst
- immigration compliance officer
- gaming compliance officer
- ethics compliance officer




