Talent.com
Manager, Regulatory Affairs

Manager, Regulatory Affairs

Adicet BioRedwood City, CA, US
job_description.job_card.variable_days_ago
serp_jobs.job_preview.job_type
  • serp_jobs.job_card.full_time
job_description.job_card.job_description

Manager, Regulatory Affairs

Adicet Bio is seeking a highly motivated Manager, Regulatory Affairs, who is passionate in the field of cell therapy development for oncology and autoimmune patients. He / she is a curious learner, dedicated, highly focused, and welcomes unexpected challenges. The desired candidate must be a team player and enjoy a fast-paced, dynamic work environment.

The Manager will report into the Regulatory group devoted to developing regulatory strategies that support rapid clinical and product development of cell therapies. He / she will be responsible for managing the global regulatory implementation of assigned projects in early to late-stage development. The successful candidate will interface cross-functionally in a matrixed environment to ensure planning, coordination, and communication for development of timely and robust regulatory strategies and submissions to meet overall program objectives / milestones.

Key responsibilities :

  • Support the regulatory function in assigned projects to drive global regulatory
  • Provide regulatory strategy, guidance and input throughout product
  • Manage the preparation and filing of regulatory applications, commitments, and change amendments. Author and review regulatory documents to ensure that all submissions are of high
  • Support the preparation and conduct of Agency meetings, including preparation and coordination of briefing packages.
  • Review clinical and CMC documentation, including protocols, reports, DSUR's, Investigator Brochures, change controls, certificates of analyses, etc. to ensure GxP and regulatory compliance.
  • Create and maintain regulatory timelines and track deliverables to ensure submission timelines are met for assigned projects.
  • Interface with functional areas, external partners and consultants, as
  • Maintain knowledge of current global regulations and guidance governing drugs and biologics in all phases of development.

Qualifications :

  • Strong scientific background with BA / BS degree in life sciences, pharmacy, or other related fields. Advanced degree is preferred.
  • At least five years of experience in Regulatory Affairs in the biotechnology or pharmaceutical
  • Experience in quality assurance, analytical testing, and research is
  • Knowledge and experience in interpretation of regulations and guidelines related to drug
  • The desire and ability to work in a fast-paced, start-up
  • Strong collaboration, teamwork, organizational skills, and attention to
  • Excellent written and verbal communication
  • Pay Range : $124,000 - $171,000 USD

    Adicet fosters a collaborative, high-performing environment by prioritizing in-person engagement. To enhance teamwork and communication, employees are required to be onsite at least three days per week (TuesdayThursday mandatory) , with some roles requiring full-time onsite presence.

    At Adicet, our people are our greatest focus. We believe that attracting and retaining the best and brightest is the key to achieving our mission to deliver best-in-class gamma delta T cell therapies for patients fighting autoimmune diseases and cancer.

    We offer a competitive compensation package including base salary, annual cash bonus, long-term incentives (equity), Employee Stock Purchase Plan (ESPP) and a 401(k) with ROTH and a 4.5% Company match.

    To ensure the wellness of our employees and their loved ones, we offer comprehensive health plans (medical, dental, vision, etc.), Flexible Health and Commuter Spending Accounts (FSA) and a company matched Health Savings Account (HSA). We also offer a life, AD&D, short and long-term disability insurance, and legal, pet, and various other voluntary insurance programs.

    We also believe our greatest ideas come when we are refreshed and focused, and we offer generous paid time-off including 13 company holidays, paid end-of-year winter break, vacation, sick time, and paid parental leave.

    Adicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company-subsidized lunches (delivered onsite daily) and fully stocked breakrooms.

    Adicet is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

    serp_jobs.job_alerts.create_a_job

    Regulatory Manager • Redwood City, CA, US

    Job_description.internal_linking.related_jobs
    • serp_jobs.job_card.promoted
    Regulatory Affairs CMC Director

    Regulatory Affairs CMC Director

    ExelixisAlameda, CA, United States
    serp_jobs.job_card.full_time
    Provide Regulatory Affairs CMC expertise and leadership for global commercial and development projects.Develop strategic approaches to enable succesful Health Authority submissions and communicatio...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Regulatory Affairs Project Manager

    Regulatory Affairs Project Manager

    AbbottAlameda, CA, US
    serp_jobs.job_card.full_time
    Regulatory Affairs Project Manager.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 hea...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Director, Regulatory Affairs

    Director, Regulatory Affairs

    Revolution MedicinesRedwood City, CA, US
    serp_jobs.job_card.full_time
    Director of Regulatory Affairs.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Manager, Regulatory Affairs

    Manager, Regulatory Affairs

    Gilead Sciences, Inc.Foster City, CA, United States
    serp_jobs.job_card.full_time +1
    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 therapi...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Technical Lead

    Regulatory Affairs Technical Lead

    IntuitiveSunnyvale, CA, US
    serp_jobs.job_card.full_time
    Regulatory Affairs Technical Lead.At Intuitive, we are united behind our mission : we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we exp...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    Pacer GroupSan Mateo, CA, US
    serp_jobs.job_card.full_time
    Job Title : PRC Submission Management Lead.Location : Foster City, CA 94404 (Hybrid).Seeking a seasoned PRC Submission Management Lead to support the CPC team. This specialized role requires deep expe...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    ACL DigitalFoster City, CA, US
    serp_jobs.job_card.full_time
    Job title : PRC Submission Management Lead.Client is seeking a seasoned PRC Submission Management Lead to support the CPC team. This specialized role requires deep expertise in the Medical, Legal, an...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    ApTaskSan Mateo, CA, US
    serp_jobs.job_card.full_time
    The client is a leading American biopharmaceutical company.It specializes in the discovery, development, and commercialization of innovative therapeutics, particularly in antiviral drugs for HIV, h...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager Heart Failure (on-site)

    Regulatory Affairs Manager Heart Failure (on-site)

    AbbottPleasanton, CA, US
    serp_jobs.job_card.full_time
    We are seeking a Regulatory Affairs Manager to join Abbott's Heart Failure Division on-site in Pleasanton, CA.As an individual contributor, the function of a Regulatory Affairs Manager is to combin...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Director, Regulatory Affairs

    Director, Regulatory Affairs

    GileadSan Mateo, CA, US
    serp_jobs.job_card.full_time
    Director, Virology Global Regulatory Affairs.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 can...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Director of Regulatory Affairs (San Jose)

    Director of Regulatory Affairs (San Jose)

    Connect Life ScienceSan Jose, CA, US
    serp_jobs.job_card.part_time
    Senior Director of Regulatory Affairs.Hybrid working - some travel to Bay Area.Competitive compensation + strong benefits. Director of Regulatory Affairs.US and a passion for mentorship, cross-funct...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    Calyxo, Inc.Pleasanton, CA, United States
    serp_jobs.job_card.full_time
    The company was founded in 2016 to address the profound need for improved kidney stone treatment.Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resourc...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    Katalyst Healthcares & Life SciencesSan Jose, CA, US
    serp_jobs.job_card.full_time
    Responsibilities : Regulatory submissions including original ANDAs, amendments, annual reports, supplements and PADERs to company applications. Preparation / review of original submission / amendments / su...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
    • serp_jobs.job_card.promoted
    Director of Regulatory Affairs

    Director of Regulatory Affairs

    Connect Life ScienceAlameda, CA, US
    serp_jobs.job_card.full_time
    Senior Director of Regulatory Affairs.Hybrid working - some travel to Bay Area.Medical Devices – Class III.Competitive compensation + strong benefits. Director of Regulatory Affairs.US and a p...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    StaffingSan Mateo, CA, US
    serp_jobs.job_card.full_time
    Join A Global Leader In Workforce Solutions Net2source Inc.Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the ta...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager •

    Regulatory Affairs Manager •

    StaffingSan Mateo, CA, US
    serp_jobs.job_card.full_time
    Prc Submission Management Lead.Location : FC Hybrid BR : • • • / HR True Job title : PRC Submission Management Lead • • • Sciences is seeking a seasoned PRC Submission Management Lead to support the CPC tea...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager •

    Regulatory Affairs Manager •

    eTeamSan Mateo, CA, US
    serp_jobs.job_card.full_time
    Regulatory Affairs Manager, Prc Submission Management Lead.Serve as a subject matter expert (SME) in US CPC team, ensuring compliance with regulatory standards and internal processes.Manage end-to-...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
    • serp_jobs.job_card.promoted
    Regulatory Affairs Manager (New Created Position)

    Regulatory Affairs Manager (New Created Position)

    AllerganSan Francisco, CA, United States
    serp_jobs.job_card.full_time
    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable i...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30