regulatory Jobs in Minneapolis, MN

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Assistant Director Regulatory Affairs

Zachary Piper Solutions, LLC

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Eden Prairie, Minnesota, USA

Full-time

Piper Companies is looking for an Assistant Director of Regulatory Affairs to join a biotechnology company focusing on products to address life threatening conditions. This is a full-time position and onsite in Eden Prairie, MN (relocation assistance available). Essential Duties of the Assistant Director of Regulatory Affairs: Main point person responsible for writing INDs. 50-60% of time will be writing related. Writing sections of IND with support of cross functional teams. Opportunity to gai
Posted 1 day ago | Updated 10 hours ago

Regulatory Project/Program Manager (Product DNA ecosystem)

Tellus Solutions

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Remote

Contract

Job Description:As a key team member, the Sr. Regulatory Project Manager-Product DNA brings a leadership opportunity to make an impact supporting the Healthcare Product DNA Program; a major transformational program that will create a connected thread of non-transactional product data to support the entire product lifecycle. This will specifically drive changes and interfaces within our overall eco-system (PLM, MES and ERP). This program is planned as a multi- year program that will have multiple
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Posted 9 hours ago

Regulatory Coordinator (Beauty/cosmetic/Personal care industry)

Apidel Technologies

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Remote

Contract

Position: Regulatory Coordinator Location: Remote Duration: 6 months (High possibilities of Extension) Skills Required / Desired Amount of Experience Familiarity with PCPC ingredient database, INCI s, cosmetic ingredients and functions and product registration is a must Required Working knowledge of EU, US and other global cosmetic, chemical and environmental regulations Required minimum of 3-5 years regulatory experience in the cosmetic, personal care, or related industry Required Bachelor s d
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Posted 1 day ago

Regulatory affairs - CMC Manager

Sureminds Solutions

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Remote

Full-time

PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5+ years in the pharmaceutical industry, preferably with 3+ years CMC regulatory experience, Sterile Injectable experience preferred. Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for post-approval small molecule product submissions, including global supplements/variations and responses to health authority queries. 2. Prep
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Posted 20 days ago

Regulatory Change Management Specialist

Randstad Digital

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Remote or New Jersey, USA

Contract

job summary: Summary: This role is responsible for developing and executing the change strategy to support processes, tools, and techniques that manage the people side of change. The goal is to achieve business objectives and outcomes while ensuring alignment across multiple projects within a program. The position also maintains delivery standards in accordance with established Change Management methodologies. location: Mount Laurel, New Jersey job type: Contract work hours: 8am to 5pm educ
Posted 60+ days ago | Updated moments ago

Internal Auditor- Regulatory

Evoke Technologies

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Remote

Full-time

Job Title - Internal Auditor- Regulatory Number of Positions - 12 Job Start Date - 6/19/25 Job End Date - 12/31/25 Location: Remote Number of Positions: 12 Level: Associate and Senior Associate Global Banking Practice is seeking a highly skilled and motivated Internal Auditor Regulatory at the Senior Associate level for a fully remote opportunity. This individual will support internal audit engagements and regulatory validation efforts for large banking clients, with a strong focus on core inter
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Posted 2 days ago | Updated 1 day ago

Regulatory affairs - CMC Manager

Sureminds Solutions

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Remote

Contract

Title : Regulatory affairs - CMC Manager Location: Remote This will be 100% remote in the US only PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5+ years in the pharmaceutical industry, preferably with 3+ years CMC regulatory experience, Sterile Injectable experience preferred. Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for post-approval small molecule product su
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Posted 20 days ago

Internal Auditor -- Regulatory

Evoke Technologies

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Remote

Contract

Key Responsibilities:Lead and execute core internal audit activities, including planning, fieldwork, control testing, and reporting in accordance with IIA standards.Perform risk-based assessments and evaluate the design and operating effectiveness of internal controls, including those related to regulatory reporting, finance data, Identity and Access Management (IAM), and corporate functions.Support regulatory issue management, including validating remediation activities and ensuring sustainabil
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Posted 6 days ago

Remote : SAP Finance4U Regulatory Reporting

SoftPath Technologies LLC

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US

Contract, Third Party

Hi, Greetings For The Day, I'm Sushmitha from SoftPath Technologies LLC and works in a Recruitment. We have a position for SAP Finance4U Regulatory Reporting @ Remote with our client and your profiles matches to requirement. Can you please check below JD and if you are interested then please share your updated resume to Skill: SAP Finance4U Regulatory Reporting Location : Remote With Occasional Travel Duration : Long Term Exp: 10-12+yrs Job Description / Responsibilities: Consulting Services:
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Posted 60+ days ago | Updated 19 hours ago

Senior Regulatory Affairs SME

LMI Government Consulting (Logistics Management In

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Remote

Contract

Overview LMI is seeking a Senior Regulatory Affairs SME to support the Biomedical Advanced Research and Development Authority (BARDA). This position can likely be performed remotely. This position requires the ability to obtain a public trust clearance. The Biomedical Advanced Research and Development Authority (BARDA) was established to support and advance the development of vaccines, therapeutics, diagnostics, and innovative technologies for use during public health emergencies. Candidates w
Posted 60+ days ago | Updated 9 hours ago

Hard Goods Regulatory Engineering Risk and Compliance Manager

3M Company

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Remote or Maplewood, Minnesota, USA

Full-time

Job Description: Hard Goods Regulatory Engineering Risk and Compliance Manager Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, cre
Posted 1 day ago | Updated moments ago

Director, Global Regulatory Affairs (Business Integration Lead)

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 2 days ago | Updated moments ago

Regulatory Data Analyst (Remote)

First American Financial Corporation

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Remote or Fort Mill, South Carolina, USA

Full-time

Who We Are ServiceMac is a new sub-servicing entity backed by some of the leading practitioners of the mortgage servicing industry. ServiceMac is focused on providing superior technology, products, and services for the mortgage and real estate industries backed by highly personalized service and support. Through continuous innovation and acquisition, our offerings comprise of personalized solutions that span the mortgage continuum and enhance security, compliance, customer satisfaction, and prof
Posted 5 days ago | Updated moments ago

Director, Data Regulatory Advisory & Management Lead, C15

Citi

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Remote or New York, New York, USA

Full-time

The Data Regulatory Advisory & Management team within the Enterprise Data Office's (EDO) Business Enablement and Data Governance group leads messaging on Citi's Consent Order commitments, and progress against them, to regulators, senior management, and Board. This includes leadership on significant regulatory correspondence; Consent Order Quarterly Progress Reporting; agenda-setting and content development for data-related regulatory reporting and meetings (both routine and rapid response); cont
Posted 16 days ago | Updated moments ago

VP, Data Analytics Lead Analyst (Financial regulatory reporting) C13

Citi

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Remote or Jacksonville, Florida, USA

Full-time

Citi, the leading global bank, has approximately 200 million customer accounts and does business in more than 160 countries and jurisdictions. Our core activities are safeguarding assets, lending money, making payments and accessing the capital markets on behalf of our clients. Citi's Mission and Value Proposition explain what we do and Strategy explain how we do it. Our mission is to serve as a trusted partner to our clients by responsibly providing financial services that enable growth and ec
Posted 34 days ago | Updated moments ago

Data Regulatory Execution Lead Analyst - VP - New York (Hybrid)

Citi

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Remote or New York, New York, USA

Full-time

About the team: As part of the Risk Data Transformation team of the Enterprise Data Office, you will be part of a team responsible to: Establish, maintain, and communicate the Risk Data transformation strategyDrive the remediation and adoption of consistent data management standards and capabilities to support the Enterprise Risk Management Framework across the enterprise and relevant businesses / functions / regions. About the role: The Citi Data Governance Policy (CDGP) provides a framework
Posted 34 days ago | Updated moments ago

Extrusion Engineer

Katalyst Healthcares and Lifesciences

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Brooklyn Park, Minnesota, USA

Full-time

Roles & Responsibilities: Provide critical support on LEANPD-driven new product development projects. Drive continuous improvement in existing manufacturing technologies and methods. Identify and implement new technologies to improve process control and tolerance management. Serve as a key liaison between product development and manufacturing engineering. Collaborate with Product Development teams to optimize designs for manufacturability. Develop, qualify, and document tooling and manufac
Posted 5 days ago | Updated moments ago

Senior Quality Engineer (Med Device/SaMD)

People Force Consulting Inc

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Mounds View, Minnesota, USA

Contract, Third Party

Job Description: As a Senior Quality Engineer Digital Health, you ll provide quality engineering leadership for web, mobile, and AWS-based cloud applications, including SaMD platforms. You will ensure compliance with global regulatory standards, manage risk and cybersecurity, and champion software quality throughout the development lifecycle. You ll collaborate closely with R&D, Regulatory Affairs, and Systems Engineering to deliver reliable, secure, and compliant digital health solutions. Respo
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Posted 2 days ago | Updated 18 hours ago

Validation Engineer III

Katalyst Healthcares and Lifesciences

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Mounds View, Minnesota, USA

Full-time

Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Perform, oversee, and guide supplier process validations (IQ/OQ/PQ) for sterile barrier packaging material manufacturing processes. Ensure supplier process validation requirements (CTQs, drawings, specifications, risk levels, and protocols) are communicated, understood, and executed. Collaborate with suppliers to review and approve validation documentation, including prot
Posted 7 days ago | Updated moments ago

R&D Engineer (specialist)

Katalyst Healthcares and Lifesciences

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Minneapolis, Minnesota, USA

Full-time

Responsibilities: Design and develop test methods to support additional studies. pply engineering principles to product design analysis and assessment. Produce engineering reports to provide technical explanation to support domestic and international regulatory submissions. Leverage engineering knowledge in conducting complaint evaluations and CAPA investigations to understand potential device failures. Prepare technical product documentation including design history files, drawings, bills of ma
Posted 7 days ago | Updated moments ago