All roles

[Remote] Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

Remote · USA Full-time New today

Note: The job is a remote job and is open to candidates in USA. Stryker is a leading company in innovative medical products and services, and they are seeking a Staff Regulatory Affairs Specialist in Pharmaceuticals. This role focuses on supporting fluorescence imaging drug products and involves preparing regulatory submissions, ensuring compliance, and advising personnel on regulatory pathways.

Responsibilities

  • Support regulatory submission strategies and update as needed through investigation and evaluation of regulatory history/ background, classification, disease, and/ or harmonized/ recognized standards, in order to assess regulatory implications for approval
  • Assess the acceptability of quality, nonclinical and clinical documentation for submission filings to comply with regulatory requirements for clinical investigations and marketing applications and corporate goals, to secure submission approval
  • Prepare submissions and/ or documents supporting submissions (i.e., CTD summaries) to gain approvals for clinical investigations and/ or commercial distribution, such as: CTAs, INDs, ITAs, (s)NDAs, DINAs, Marketing Authorizations (MA) and Letters to File etc
  • Ensure that the quality, nonclinical and/or clinical data, in conjunction with regulatory strategy, are consistent with the regulatory requirements and support the proposed product claims
  • Develop and maintain positive relationships with regulatory agencies through oral and written communications regarding regulatory agency meetings, potential regulatory pathways, clarification, and follow-up of submissions under review
  • Advise personnel on regulatory requirements for quality, nonclinical and clinical data requirements for clinical study applications and/ or marketing applications
  • Contribute to evaluations of the regulatory environment and provide regulatory input to product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance
  • Demonstrate strong project management, writing, coordination, and execution of regulatory items, with emphasis on technical and scientific regulatory activities
  • Possess and apply a broad and advanced knowledge, skills/abilities and understanding of the regulatory and legal frameworks, regulatory requirements, legislation, processes, and procedures

Skills

  • Bachelor's Degree
  • 4+ years of experience in an FDA regulated industry
  • 2+ years of pre- and/or post-market Regulatory Affairs experience
  • Experience preparing submissions and/ or documents supporting submissions (i.e., CTD summaries) to gain approvals for clinical investigations and/or commercial distribution
  • Ability to comply with constantly changing regulatory and clinical environments and prioritize work effectively
  • Ability to understand and explain detailed regulatory compliance programs and/or issues
  • Adaptable to a fast-paced environment with changing circumstances, direction and strategy and has the desire to thrive in a dynamic environment
  • Bachelor's Degree in Health Science or equivalent focus
  • RAC certification or Advanced Degree (Masters in Regulatory Affairs)
  • 4+ years of regulatory affairs experience within pharmaceuticals

Benefits

  • Medical and prescription drug insurance
  • Dental insurance
  • Vision insurance
  • Critical illness insurance
  • Accident insurance
  • Hospital indemnity insurance
  • Personalized healthcare support
  • Wellbeing program
  • Tobacco cessation program
  • Health Savings Account (HSA)
  • Flexible Spending Accounts (FSAs)
  • 401(k) plan
  • Employee Stock Purchase Plan (ESPP)
  • Basic life and AD&D insurance
  • Short-term disability insurance

Company Overview

  • Stryker is a medical technology company that offers products and services in orthopaedics. It was founded in 1941, and is headquartered in Kalamazoo, Michigan, USA, with a workforce of 10001+ employees. Its website is http://www.stryker.com/en-us/index.htm.

Company H1B Sponsorship

  • Stryker has a track record of offering H1B sponsorships, with 105 in 2025, 76 in 2024, 63 in 2023, 78 in 2022, 57 in 2021, 77 in 2020. Please note that this does not guarantee sponsorship for this specific role.

Apply tot his job Apply To this Job Apply tot his job Apply To this Job

Related roles

[Remote] Regulatory Affairs Specialist

Remote · USA Full-time

Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

Remote · USA Full-time

Regulatory Affairs Specialist II - Remote

Remote · USA Full-time

Regulatory Affairs Consultant- Defined Term (Remote, US)

Remote · USA Full-time

Regulatory Affairs Consultant- Defined Term (Remote, US)

Remote · USA Full-time

Sr. Regulatory Affairs Specialist - REMOTE

Remote · USA Full-time

Lead Regulatory Affairs Licensing Engineer (remote eligible)

Remote · USA Full-time

Hiring Regulatory Affairs Associate II (Hybrid Remote)

Remote · USA Full-time

Amgen Senior Associate – Regulatory Affairs (US-Remote) in Los Angeles, California

Remote · USA Full-time

Program Manager, Federal Regulatory Affairs

Remote · USA Full-time

Experienced Customer Service Representative – Remote Opportunity with arenaflex

Remote · USA Full-time

Experienced Technical Customer Care Specialist - Night Shift - Remote

Remote · USA Full-time

Remote Data Entry Specialist for UPS Job

Remote · USA Full-time

Project Manager - Patient Monitoring

Remote · USA Full-time

AI Transformation Strategist (Mexico/Remote) - Truelogic Software

Remote · USA Full-time

Experienced Virtual Customer Service Representative – Delivering Exceptional Customer Experiences at arenaflex

Remote · USA Full-time

Bilingual French English Travel Consultant

Remote · USA Full-time

AEM Product Manager

Remote · USA Full-time

Student Online typing jobs from home

Remote · USA Full-time

Experienced Customer Service Representative - Phone, Chat, Email, and Social Media Support for Educational Website

Remote · USA Full-time