regulatory affairs Jobs in illinois

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Regulatory Affairs Ops Specialist I

Pyramid Consulting, Inc.

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Deerfield, Illinois, USA

Contract

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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Posted 1 day ago

Regulatory Affairs Operations Specialist

Accord Innovations Sdn Bhd

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Deerfield, Illinois, USA

Contract, Third Party

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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Posted 1 day ago

Regulatory Affairs Ops Specialist -Deerfield, IL

Cube Hub, Inc.

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Deerfield, Illinois, USA

Third Party, Contract

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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Posted 1 day ago | Updated 1 day ago

Regulatory Affairs Ops Specialist

Valueprosite

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Deerfield, Illinois, USA

Contract

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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Posted 1 day ago

Senior Regulatory Affairs Licensing Engineer (remote eligible)

GE Vernova

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Remote

Full-time

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
Posted 6 days ago | Updated 12 hours ago

Principle Regulatory Engineer

Constellation Energy

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Clinton, Illinois, USA

Full-time

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
Posted 8 days ago | Updated 12 hours ago

Regulatory CMS Senior Manager

Sureminds Solutions

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Remote

Contract, Third Party

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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Posted 5 days ago | Updated 4 days ago

Engineer, Principal Regulatory

Constellation Energy

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Byron, Illinois, USA

Full-time

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
Posted 47 days ago | Updated 9 hours ago

Engineer, Principal Regulatory

Constellation Energy

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Byron, Illinois, USA

Full-time

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
Posted 47 days ago | Updated 19 hours ago

Engineer, Principal Regulatory

Constellation Energy

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Byron, Illinois, USA

Full-time

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
Posted 60+ days ago | Updated 12 hours ago

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

Boeing Company

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Remote or Dallas, Texas, USA

Full-time

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 established classification methodologies utilizing the Harmonized Tariff Schedule and Order of Revie
Posted 6 days ago | Updated 12 hours ago

Data Risk Appetite Sr Group Manager, Director

Citi

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Remote or New York, New York, USA

Full-time

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
Posted 18 days ago | Updated 12 hours ago

Principal Engineer, R&D NPI Lead

Johnson & Johnson

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Remote or Jacksonville, Florida, USA

Full-time

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
Posted 7 days ago | Updated 12 hours ago

Principal Regulatory Consultant Dietary Supplements

Apptad Inc

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New Jersey, USA

Contract, Third Party

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
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Posted 19 days ago

Associate Director - Hematology, Oncology Data Sciences & Digital Health

Johnson & Johnson

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Remote or New Brunswick, New Jersey, USA

Full-time

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
Posted 43 days ago | Updated 12 hours ago

Senior Manager, Data Analytics

Quest Diagnostics Inc.

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Chicago, Illinois, USA

Full-time

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
Posted 6 days ago | Updated 12 hours ago

Sr. Principal Engineer, R&D

Johnson & Johnson

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Remote or Raritan, New Jersey, USA

Full-time

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
Posted 3 days ago | Updated 12 hours ago

Computer System Validation Analyst - R Studio & Clinical Systems

Katalyst Healthcares and Lifesciences

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Remote or New Jersey, USA

Full-time

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
Posted 60+ days ago | Updated 12 hours ago

Associate Director, Process Engineering

Takeda pharmaceutical

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Round Lake, Illinois, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: At Takeda's Round Lake aseptic fill/finish and Packaging facility, the Associate Director, Process Engineering will
Posted 60+ days ago | Updated 12 hours ago

Sr Manager, IT Business Analysis - SAP BRH Architect

Gilead Sciences, Inc.

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Remote or Foster City, California, USA

Full-time

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical ro
Posted 21 days ago | Updated 12 hours ago