Talent.com
Principal Specialist, Regulatory Affairs

Principal Specialist, Regulatory Affairs

ImmunityBioSummit, NJ, US
30+ days ago
Job type
  • Full-time
Job description

Principal, Specialist, Regulatory Affairs

ImmunityBio, Inc. (NASDAQ : IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal : to reprogram the patient's immune system and treat the host rather than just the disease.

Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California. Work with a collaborative team with the ability to work across different areas of the company. Ability to join a growing company with professional development opportunities.

Position Summary

The Principal, Specialist, Regulatory Affairs will provide expertise to the organization in the development of regulatory compliance strategies and in ensuring its conformance to Health Authority requirements.

Essential Functions

  • Lead and prepare FDA submissions, by collaborating with all disciplines within the organization.
  • Assist with developing and evaluating regulatory strategy.
  • Responsible for maintaining compliance with US and International Health Authority regulations for products under development and for marketed products.
  • Serve as a Regulatory Affairs subject matter expert to the Regulatory Affairs team and organization.
  • Approve, review, or prepare common technical documents (CTD) for technical content and compliance with regulatory requirements
  • Keep abreast of internal and external changes, trends, and developments to the regulatory environment that may have an impact on ImmunityBio products.
  • Author and review departmental SOPs, as well as other SOPs that may impact Regulatory Affairs.
  • Performs other special projects and duties as requested.

Education & Experience

  • Bachelor's Degree in life sciences required; Master's degree preferred
  • 10+ years of relevant regulatory compliance experience in pharmaceutical drug development and manufacturing required
  • Knowledge and experience with organizing responses to Regulatory Authority requests required
  • Experience with US and International Health Authority regulatory submissions preferred
  • Knowledge, Skills, & Abilities

  • Knowledge of FDA, ICH and other guidance documents and requirements
  • Knowledge of organizing responses to Regulatory Authority requests
  • Strong knowledge of Health Authority regulatory requirements / guidelines
  • Strong project management and computer skills (including Microsoft office)
  • Strong document management experience (hard and e-copy)
  • Ability to work with firm deadlines and adapt quickly to changing requirements and priorities
  • Strong organizational skills, written / oral communication skills and attention to detail
  • Ability to manage conflicting priorities and respond in a timely, effective manner
  • Working Environment / Physical Environment

  • This is a full-time position (40 hours per week) Monday through Friday.
  • This role may need to sit for long periods of time and use various computer programs.
  • This desk-based role involves the close study of scientific and regulatory documents.
  • They will work closely with scientific colleagues throughout the day, often on a project team basis.
  • This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

    $162,000 (entry-level qualifications) to $180,000 (highly experienced) annually

    The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

    ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include : Medical, Dental and Vision Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life / AD&D, Short-Term and Long-Term Disability Healthcare and Dependent Care Flexible Spending Accounts 401(k) Retirement Plan with Company Match 529 Education Savings Program Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks Paid Time Off (PTO) includes : 11 Holidays Exempt Employees are eligible for Unlimited PTO Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

    At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and / or expression, or other status protected by law.

    Create a job alert for this search

    Regulatory Specialist • Summit, NJ, US

    Related jobs
    • Promoted
    • New!
    Manager Regulatory Affairs Operations

    Manager Regulatory Affairs Operations

    New Jersey StaffingPrinceton, NJ, US
    Full-time
    Acadia Pharmaceuticals Job Posting.Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities a...Show moreLast updated: 12 hours ago
    • Promoted
    Regulatory Affairs Director - Oncology

    Regulatory Affairs Director - Oncology

    AstraZenecaNew York, NY, US
    Full-time
    Would you like to apply your Regulatory Affairs strategy expertise and passion to make an impact in a company that follows the science and turns ideas into life changing medicines?.At AstraZeneca, ...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Specialist

    Regulatory Specialist

    ChubbNew York, NY, US
    Full-time
    This is the job title and description.No extra metadata, links, buttons, or any other unnecessary information has been included. The content is focused and clean, ensuring a high signal to noise rat...Show moreLast updated: 27 days ago
    • Promoted
    Director Regulatory Affairs Strategy

    Director Regulatory Affairs Strategy

    Lynkx Staffing LLCPrinceton, NJ, US
    Full-time
    Our Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of ...Show moreLast updated: 30+ days ago
    • Promoted
    Executive Director Global Regulatory Affairs

    Executive Director Global Regulatory Affairs

    EPM ScientificNutley, NJ, US
    Full-time
    A leading global biopharmaceutical organization is seeking a seasoned.Executive Director of Global Regulatory Strategy.This is a high-impact, hands-on leadership role ideal for a strategic thinker ...Show moreLast updated: 30+ days ago
    • Promoted
    Senior Director, Regulatory Affairs

    Senior Director, Regulatory Affairs

    Formation BioNew York, NY, US
    Full-time
    Senior Director, Regulatory Affairs.Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creati...Show moreLast updated: 18 days ago
    • Promoted
    • New!
    Senior Regulatory Affairs Specialist

    Senior Regulatory Affairs Specialist

    New Jersey StaffingMontvale, NJ, US
    Full-time
    Senior Regulatory Affairs Specialist.Our mission is to improve the standard of patient care and quality of healthcare delivery by providing the best endoscopic products and services with a focus on...Show moreLast updated: 12 hours ago
    • Promoted
    Regulatory Affairs Specialist (Hybrid)

    Regulatory Affairs Specialist (Hybrid)

    Spectrum VascularBridgewater, NJ, US
    Full-time
    Spectrum Vascular is an innovative medical device company focused on vascular access and medication management.Our mission is to improve the lives of patients worldwide by providing caregivers with...Show moreLast updated: 21 days ago
    • Promoted
    Senior Manager, Global Regulatory Affairs, Strategy

    Senior Manager, Global Regulatory Affairs, Strategy

    GenmabPrinceton, NJ, US
    Full-time
    Senior Manager Regulatory Affairs Strategy.Genmab is looking for a Senior Manager, Global Regulatory Affairs, Regulatory Strategy to be a part of our Global Regulatory Affairs organization.In this ...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Affairs Specialist II

    Regulatory Affairs Specialist II

    Katalyst Healthcares & Life SciencesSecaucus, NJ, US
    Full-time
    Regulatory Submission Specialist.This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U. Europe, support of international product...Show moreLast updated: 30+ days ago
    • Promoted
    • New!
    Director Regulatory Affairs

    Director Regulatory Affairs

    New Jersey StaffingPrinceton, NJ, US
    Full-time
    Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. Join us, the future is ours to shape!...Show moreLast updated: 12 hours ago
    • Promoted
    Regulatory Affairs Specialist III

    Regulatory Affairs Specialist III

    HireTalentBound Brook, NJ, US
    Full-time
    Regulatory Affairs Specialist III.Location : Bridgewater, NJ Duration : 9 Months.Manager will consider candidates to be based in either Bridgewater, New Jersey or Cambridge, Massachusetts.Please spec...Show moreLast updated: 30+ days ago
    • Promoted
    Director of Regulatory Affairs

    Director of Regulatory Affairs

    Evolution Research GroupNew Providence, NJ, US
    Full-time
    Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and...Show moreLast updated: 30+ days ago
    • Promoted
    Manager Regulatory Affairs Operations

    Manager Regulatory Affairs Operations

    Acadia PharmaceuticalsPrinceton, NJ, US
    Full-time
    Please note that this position is based in San Diego, CA, or Princeton, NJ.Acadia's hybrid model requires this role to work in our office three days per week on average. The Regulatory Operations Ma...Show moreLast updated: 3 days ago
    • Promoted
    Global Regulatory Affairs Compliance and Planning, Sr. Manager

    Global Regulatory Affairs Compliance and Planning, Sr. Manager

    Kyowa KirinPrinceton, NJ, US
    Full-time
    Kyowa Kirin is a global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four areas of unmet need : oncology, nephrology, imm...Show moreLast updated: 30+ days ago
    • Promoted
    Senior Director, Regulatory Affairs

    Senior Director, Regulatory Affairs

    Formation Bio (Formerly TrailSpark)New York, NY, US
    Full-time
    Senior Director, Regulatory Affairs.Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creati...Show moreLast updated: 18 days ago
    • Promoted
    Specialist, U.S. Commercial Regulatory Affairs Operations

    Specialist, U.S. Commercial Regulatory Affairs Operations

    Bristol Myers SquibbPrinceton, NJ, US
    Full-time
    Promotional Review Editor (PRE) Specialist.Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happen...Show moreLast updated: 14 days ago
    • Promoted
    Staff Regulatory Affairs Specialist

    Staff Regulatory Affairs Specialist

    Becton DickinsonFranklin Lakes, NJ, US
    Full-time
    The Staff RA Specialist will represent Regulatory Affairs within the Worldwide Infusion Preparation and Delivery (WWIPD) platform on compliance projects, product engineering, new product developmen...Show moreLast updated: 30+ days ago