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Regulatory Affairs Operations Specialist

Deerfield, Illinois

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4d ago

We are seeking a detail-oriented and experienced Regulatory Affairs Operations Specialist to join our team in Deerfield, IL! This is an onsite role ideal for professionals with a strong background in regulatory documentation, SOPs, and compliance. What You'll Do: Implement regulatory strategies and resolve submission-related issues Maintain electronic regulatory records and manage data integrity during system upgrades Collaborate cross-functionally to support compliance and project success

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Contract, Third Party

Depends on Experience

Regulatory Affairs Ops Specialist I

Deerfield, Illinois

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4d ago

Immediate need for a talented Regulatory Affairs Ops Specialist I. This is a 12+ months contract opportunity with long-term potential and is located in Deerfield, IL(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-80529 Pay Range: $45 - $48/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: This section f

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Contract

$45 - $48

Regulatory Affairs Ops Specialist -Deerfield, IL

Deerfield, Illinois

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Today

Regulatory Affairs Ops Specialist Deerfield, IL 12 months Description: This section focuses on the main purpose of the job in one to four sentences. Under limited supervision responsible for the implementation of regulatory strategies, and resolution of issues pertaining to documents/ packages for regulatory submissions. Produces and evaluates technical and scientific data necessary for regulatory submissions. Assists in the implementation and delivery of new or upgraded systems and processes

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Contract, Third Party

$DOE

Regulatory Affairs Ops Specialist

Deerfield, Illinois

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4d ago

Title: Regulatory Affairs Ops Specialist Type: Hybrid 1 Baxter Parkway Deerfield Illinois 60015 United States Duration: 12 months Key Responsibilities: Under limited supervision responsible for the implementation of regulatory strategies, and resolution of issues pertaining to documents/ packages for regulatory submissions.Produces and evaluates technical and scientific data necessary for regulatory submissions.Assists in the implementation and delivery of new or upgraded systems and processes i

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Contract

Depends on Experience

Senior Regulatory Affairs Licensing Engineer (remote eligible)

Remote

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Today

Job Description Summary The Regulatory Affairs Lead Licensing Engineer will lead the completion of various regulatory work scopes, including working with GEH / GNF Engineering on major projects for the existing fleet of nuclear reactors. Guided by professional practices and policies that are shaped by the role. The role has moderate autonomy, requiring high levels of operational judgment. Job Description Essential Responsibilities As a Senior Regulatory Affairs Licensing Engineer you will: Coo

Full-time

USD 111,000.00 - 162,000.00 per year

Principle Regulatory Engineer

Clinton, Illinois

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Today

WHO WE ARE As the nation's largest producer of clean, carbon-free energy, Constellation is focused on our purpose: accelerating the transition to a carbon-free future. We have been the leader in clean energy production for more than a decade, and we are cultivating a workplace where our employees can grow, thrive, and contribute. Our culture and employee experience make it clear: We are powered by passion and purpose. Together, we're creating healthier communities and a cleaner planet, and our

Full-time

USD 146,700.00 - 163,000.00 per year

Principle Regulatory Engineer

Clinton, Illinois

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Today

Full-time

USD 146,700.00 - 163,000.00 per year

Regulatory CMS Senior Manager

Remote

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7d ago

C2C Role Please share Profiles at Hi, Urgent need, Job Title: Regulatory Studio CMS Senior Manager Work location: New Brunswick (preferred), Lawrenceville Monday thru Friday - Normal business hours, with some flexibility 50% onsite - Team is onsite Monday thru Thursday Top 3 to 5 skills/Must Haves: Small Molecule Drug development experience (2 to 3 years) Good communications skills (written/verbal) Experience with Veeva System PREREQUISITES BS/BA degree in Scientific Discipline (master's or hig

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Contract, Third Party

$50 - $60

Engineer, Principal Regulatory

Byron, Illinois

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Today

Full-time

USD 146,700.00 - 163,000.00 per year

Engineer, Principal Regulatory

Byron, Illinois

•

Today

Full-time

USD 146,700.00 - 163,000.00 per year

Engineer, Principal Regulatory

Byron, Illinois

•

Today

Full-time

USD 146,700.00 - 163,000.00 per year

Data Risk Appetite Sr Group Manager, Director

Remote or New York, New York

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Today

The Data Risk Appetite Sr Group Manager, Director is a senior level role managing a team responsible for facilitating all aspects of the Enterprise Data Risk and Control Framework and Data Risk Taxonomy. This role is responsible for Quarterly : Top Risk Alignment : Data Risk metricsRisk Appetite AssessmentScenario Analysis and Lessons LearnedData Risk ProfileMetric Adequacy AssessmentRisk Appetite analyticsMetric Maturity AssessmentMetric Coverage of the categoryIssues : thematic analysisLosses

Full-time

USD 170,000.00 - 300,000.00 per year

Classification and Trade Data Specialist (Mid-Level or Senior)

Remote or Dallas, Texas

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Today

Classification and Trade Data Specialist (Mid-Level or Senior) Company: The Boeing Company The Boeing Company is seeking a Classification and Trade Data Specialist (Mid-Level or Senior) to join their team in Dallas, TX. This role ensures our products are accurately classified for importation and exportation from our nine global warehouse locations. The candidate will have a strong knowledge of aircraft parts classification utilizing the HTS, USML and CCl. Knowledge of import and export regula

Full-time

USD 83,300.00 - 112,700.00 per year

Principal Engineer, R&D NPI Lead

Remote or Jacksonville, Florida

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

Cybersecurity and Managed Services Consultant

Remote or Milwaukee, Wisconsin

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Today

Rockwell Automation is a global technology leader focused on helping the world's manufacturers be more productive, sustainable, and agile. With more than 28,000 employees who make the world better every day, we know we have something special. Behind our customers - amazing companies that help feed the world, provide life-saving medicine on a global scale, and focus on clean water and green mobility - our people are energized problem solvers that take pride in how the work we do changes the world

Full-time

USD 141,920.00 - 212,880.00 per year

Principal Regulatory Consultant Dietary Supplements

Remote or New Jersey

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22d ago

Job Description: Job Title: Principal Regulatory Consultant Dietary Supplements (U.S.-Based) Position Type: Contract / Consulting Location: Jersey City, NJ Department: Regulatory Affairs / Corporate Development Position Summary: We are seeking a highly experienced and credentialed Regulatory Consultant to support strategic M&A due diligence initiatives within the dietary supplement industry. This role demands deep understanding of the U.S. regulatory landscape, including DSHEA, FDA cGMPs (21 CFR

Easy Apply

Contract, Third Party

Associate Director - Hematology, Oncology Data Sciences & Digital Health

Remote or New Brunswick, New Jersey

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Today

Full-time

USD 137,000.00 - 235,750.00 per year

Senior Manager, Data Analytics

Chicago, Illinois

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Today

Job Description Reporting to the Director, Program Management QA/RA, the Sr. Manager, Data Analytics - Quality & Regulatory Affairs will lead the development, management, and execution of a best-in-class analytics strategy in support of the QA/RA function. This position is responsible for establishing on-going processes for collecting and transforming data into strategic insights that support risk management, regulatory compliance, operational excellence, and governance reporting. This is a hi

Full-time

USD 106,200.00 per year

Sr. Principal Engineer, R&D

Remote or Raritan, New Jersey

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Today

Full-time

USD 173,500.00 - 235,000.00 per year

Computer System Validation Analyst - R Studio & Clinical Systems

Remote or New Jersey

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Today

Responsibilities: Lead validation planning, risk assessment, and execution for R Studio, GitLab, and Medidata Rave EDC. Develop and execute validation documentation including: Validation Plans (VP.). User Requirements Specifications (URS.). Risk Assessments (RA.). Functional and Design Specifications. Traceability Matrix (RTM.). Test Protocols (IQ/OQ/PQ or CSA-based scripts.). Validation Summary Reports (VSR.). Collaborate with cross-functional stakeholders including Clinical Data Mana

Full-time

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