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Regulatory affairs associate Jobs in Saint Paul, MN

Last updated: 17 hours ago
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Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

PhilipsMinneapolis, MN, US
$75,000.00–$130,000.00 yearly
Full-time
Senior Regulatory Affairs Specialist.The Senior Regulatory Specialist will provide regulatory support for our Image Guided Therapy business including direct submission to health authorities and ind...Show moreLast updated: 17 hours ago
Manager, Global Regulatory Affairs (Hybrid)

Manager, Global Regulatory Affairs (Hybrid)

BaxterSaint Paul, MN
Full-time
This is where you save and sustain lives.At Baxter, we are deeply connected by our mission.No matter your role at Baxter, your work makes a positive impact on people around the world.You’ll feel a ...Show moreLast updated: 30+ days ago
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Regulatory Compliance Manager

Regulatory Compliance Manager

Rise Baking Company, LLCMinneapolis, Minnesota, US
$75,000.00–$100,000.00 yearly
Full-time
Lead the daily activities of the regulatory compliance team, ensuring they have the necessary tools to perform their roles and meet the deadlines and expectations of internal and external customers...Show moreLast updated: 3 days ago
Associate Director - Regulatory Program Management Office, Operations

Associate Director - Regulatory Program Management Office, Operations

Royal Bank of Canada>Minneapolis, United States of America
$85,000.00–$150,000.00 yearly
Full-time
Position reports to the US Governance Risk and Controls (GRC) Office and is responsible for.US GRC Operations provides operational support across. GRC Office, including Execution, Regulatory Affairs...Show moreLast updated: 5 days ago
Advanced Regulatory Affairs Specialist

Advanced Regulatory Affairs Specialist

Bio-TechneMinneapolis, MN
Full-time
By joining the Bio-Techne team, you will have an impact on future cutting-edge research.Bio-Techne andall ofits brands provides tools for researchers in Life Sciences and Clinical Diagnostics.The A...Show moreLast updated: 30+ days ago
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Senior Regulatory Specialist

Senior Regulatory Specialist

Fresenius Kabi USA, LLCMinneapolis, MN, United States
$103,241.25–$133,442.00 yearly
Represent Regulatory Affairs ("RA") on project teams and provide regulatory guidance.Review technical documents for cGMP and regulatory compliance. Train and coach others in regulatory requirements....Show moreLast updated: 30+ days ago
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Medical Affairs Program Manager

Medical Affairs Program Manager

ColoplastMinneapolis, MN, US
$128,529.00–$192,793.00 yearly
Full-time
The Medical Affairs Program Manager is responsible for supporting evidence strategies and for executing Coloplast agenda in the clinical community. The Chronic Care business at Coloplast has product...Show moreLast updated: 10 days ago
Sr Regulatory Affairs Spec

Sr Regulatory Affairs Spec

Real StaffingMinneapolis, Minnesota, USA
Temporary
Regulatory Affairs Specialist - Medical Device.Contract : 9 Months + potential for extension or permanent Conversion.Benefits : Real Staffing offers medical, dental, vision, 401K.W2 Employment Opport...Show moreLast updated: 30+ days ago
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Academic Affairs Associate Dean

Academic Affairs Associate Dean

ConfidentialMinneapolis, MN, United States
Full-time
Academic Affairs Associate Dean.Pioneering dental school serving the local community.Join our vibrant team as the Academic Affairs Associate Dean, where you will play a crucial role in shaping the ...Show moreLast updated: 3 days ago
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Senior Regulatory Affairs Specialist (on-site)

Senior Regulatory Affairs Specialist (on-site)

AbbottMinneapolis, MN, US
$75,300.00–$150,700.00 yearly
Full-time
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 17 hours ago
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Sr. Regulatory Affairs Specialist (Medical Device)

Sr. Regulatory Affairs Specialist (Medical Device)

The Ranger GroupMinneapolis, MN, US
Full-time
Lead Regulatory Submissions & Drive Compliance for Cutting-Edge Medical Devices!.The Ranger Group has an exciting Contract-to-Hire opportunity for a Regulatory Specialist with one of our top-tier M...Show moreLast updated: 4 days ago
Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Boston ScientificArden Hills, MN, US
The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Acts as a primary Regulatory Affairs representative in...Show moreLast updated: 30+ days ago
PPC Regulatory Affairs Manager / BP

PPC Regulatory Affairs Manager / BP

EcolabSt Paul, Minnesota, United States of America
Full-time
Pharma and Personal Care – Regulatory Affairs Manager / NA Regulatory Business Partner .At Ecolab, making the world a cleaner, safer place is our business. In our Pharmaceutical & Personal Care (PPC)...Show moreLast updated: 30+ days ago
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Regulatory Affairs Associate

Regulatory Affairs Associate

VirtualVocationsSaint Paul, Minnesota, United States
Full-time
A company is looking for a Regulatory Affairs Associate.Key ResponsibilitiesProvide daily regulatory support to achieve organizational goals and strategiesSupport third-party certification processe...Show moreLast updated: 18 hours ago
Global Respiratory Protection Regulatory Affairs Specialist

Global Respiratory Protection Regulatory Affairs Specialist

3MUS, Minnesota, Maplewood
Full-time
Global Respiratory Protection Regulatory Affairs and Standards Development Specialist, Personal Safety Division.Collaborate with Innovative 3Mers Around the World. Choosing where to start and grow y...Show moreLast updated: 15 days ago
Vice President of Regulatory, Quality & Clinical

Vice President of Regulatory, Quality & Clinical

Regulatory Affairs Professionals SocietyArden Hills, Minnesota
Full-time
Quality / Risk Management US Regulatory Affairs.Base Salary : Market-based, DOEBonus : 30%Equity.Lead Regulatory, Quality & Clinical Affairs for a Breakthrough Active Implantable Device.FDA-approved, p...Show moreLast updated: 1 day ago
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Regulatory Affairs Manager

Regulatory Affairs Manager

CollaberaMinneapolis, MN, US
$40.00–$45.00 hourly
Full-time
Contract : Minneapolis, Minnesota, US.Days Left : 15 days, 2 hours left.To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https : / / www.Regulatory Affairs...Show moreLast updated: 24 days ago
LPG Sr. Director - Quality & Regulatory Affairs

LPG Sr. Director - Quality & Regulatory Affairs

Thermo Fisher ScientificMinneapolis, Minnesota, United States of America
Full-time
Build and drive a Quality and Regulatory framework and strategy for the LPG businesses that supports growth and compliance readiness. Ensure compliance to quality and regulatory system requirements ...Show moreLast updated: 30+ days ago
Regulatory Affairs Specialist

Regulatory Affairs Specialist

Katalyst HealthCares & Life SciencesMinneapolis, MN
Author and prepare regulatory submissions for new products and changes.Review significant regulatory issues with supervisors and resolve submission issues. Develop regulatory strategies and provide ...Show moreLast updated: 30+ days ago
  • Promoted
Manager, Regulatory Compliance

Manager, Regulatory Compliance

Wilson Tool InternationalSaint Paul, MN, US
$110,000.00–$140,000.00 yearly
Full-time
The Global Compliance Leader for Wilson Tool ensures the proper implementation and adherence to compliance strategies, policies, and regulations, while ensuring Wilson Tool global entities follow r...Show moreLast updated: 15 days ago
Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

PhilipsMinneapolis, MN, US
17 hours ago
Salary
$75,000.00–$130,000.00 yearly
Job type
  • Full-time
Job description

Job Title

Senior Regulatory Affairs Specialist

Job Description

Sr. Regulatory Affairs Specialist

In this role you

The Senior Regulatory Specialist will provide regulatory support for our Image Guided Therapy business including direct submission to health authorities and indirect project management of worldwide registrations. You will execute regulatory strategy to support the growth within the Structural Heart / Heart Rhythm Management category

Your role :

  • Preparing comprehensive regulatory strategies for potentially complex new devices, and significant post market changes (such as line extensions, indication expansions, and substantive process / design changes). As necessary, reviews complex regulatory strategy issues with RA management.
  • Preparing regulatory filings for the US, EU, and Canada, potentially including FDA Pre-Submissions (and similar) for new products, as well as post-market changes. Maintain proficiency in worldwide regulatory requirements, particularly within US, EU, Canada, Japan, and China.
  • Following Philips' Quality System procedures to ensure compliance with US CFR, ISO 13485, MDD / MDR, CMDR, MDSAP, and all other applicable regulations.
  • Able to professionally negotiate and lead meetings (eg Pre-Subs) directly with regulatory agencies (e.g. FDA, Notified Bodies, etc.) on regulatory filings at the reviewer or management (eg Chief or Deputy) level.

You're the right fit if :

  • Minimum of a bachelor's degree in engineering or a related scientific field. Degree within Regulatory Affairs and / or Regulatory Affairs Certification is preferred.
  • Minimum of 5+ years of experience in the medical device industry with regulatory submission experience. 510(k) submission experience. Prefer 2+ years of experience with SaMD.
  • Proficiency in understanding, interpretation and application of FDA 21 CFR 820 Quality System Regulation, EU MDR Regulation 2017 / 745, ISO 13485, and other relevant standards and regulations.
  • Prior experience supporting / leading regulatory submissions such as 510(k), EU MDR Technical Documentation and global registrations
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office / Remote position.
  • How we work together

    We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company's facilities. Field roles are most effectively done outside of the company's main facilities, generally at the customers' or suppliers' locations.

    This is an office role.

    About Philips

    We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Learn more about our commitment to diversity and inclusion.
  • Philips Transparency Details

    The pay range for this position in Plymouth is $75,000 to $130,000, Annually.

    The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge / skills, experience, business needs, geographical location, and internal equity.

    In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here.

    At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.

    Additional Information

    US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

    Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN.

    LI-PHI

    This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.

    Philips is an Equal Employment and Opportunity Employer / Disabled / Veteran and maintains a drug-free workplace.