Senior Specialist, Regulatory Affairs

Job description

Company Overview

ImmunityBio is a vertically integrated commercial stage biotechnology company developing next-generation therapies that bolster the natural immune system to defeat cancers and infectious diseases. The Company's range of immunotherapy and cell therapy platforms, alone and together, act to drive and sustain an immune response with the goal of creating durable and safe protection against disease. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response. The Company is applying its science and platforms to treating cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies that we believe sharply reduce or eliminate the need for standard high-dose chemotherapy. These platforms and their associated product candidates are designed to be more effective, accessible, and easily administered than current standards of care in oncology and infectious diseases.

Why ImmunityBio?

* ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.

* 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 Senior 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

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

Responsible for maintaining compliance with US and International Health Authority regulations for products under development and for marketed products.

Assist with developing and evaluating regulatory strategy

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 with 7+ years of relevant regulatory compliance experience in pharmaceutical drug development required; or

Master's Degree in life sciences required with 5+ years of relevant regulatory compliance experience in pharmaceutical drug development 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.

$135,000 (entry-level qualifications) to $150,000 (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 uses artificial intelligence (AI) tools to assist with sourcing and identifying potential candidates for open positions. These tools help us reach qualified applicants and improve the efficiency of our recruitment outreach. No preference is given to applicants sourced or identified by AI tools.

Important: AI is not used to screen, evaluate, rank, assess, or make hiring decisions about applicants. All applications are reviewed by human recruiters and hiring managers. Hiring decisions are made solely by ImmunityBio personnel without automated decision-making.

We are committed to equal employment opportunity and ensure that all candidates are assessed based on their qualifications, skills, and experience through human review.

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.

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.