← all jobs

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

Work from home Full-time role Hiring

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 To this Job

More open positions

[Remote] Regulatory Affairs Specialist

Work from home Full-time role

Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

Work from home Full-time role

Regulatory Affairs Specialist II - Remote

Work from home Full-time role

Regulatory Affairs Consultant- Defined Term (Remote, US)

Work from home Full-time role

Regulatory Affairs Consultant- Defined Term (Remote, US)

Work from home Full-time role

Experienced Customer Service Representative – Remote Call Center Support

Work from home Full-time role

Physician Resident Pathways - Primary Care (Remote)

Work from home Full-time role

AI Video Trainer - Hebrew

Work from home Full-time role

Product Growth Hacker (Exchange) - Crypto.com

Work from home Full-time role

Digital and Outreach Archivist

Work from home Full-time role

Tech Lead, Web Core Product & Chrome Extension - Stockholm, Sweden

Work from home Full-time role

Regulatory Affairs Specialist - Temporary Role

Work from home Full-time role

Customer Support Agent

Work from home Full-time role

Gaming Content Moderator - Arabic

Work from home Full-time role

Experienced Senior Director, Customer Solutions – Strategic Supply Chain Leadership

Work from home Full-time role

Account Executive - Northeast

Work from home Full-time role

Signature HealthCARE – MDS Coordinator – RN – Full-Time – Columbia, KY

Work from home Full-time role

Engineering Program Lead, AI Reliability Engineering (AIRE)

Work from home Full-time role

Cloud (AWS) Engineer (DevOps Manager)

Work from home Full-time role

Sr. Android Engineer

Work from home Full-time role

Per diem Hospice Triage Nurse - Remote - MUST HAVE CA RN LICENSE

Work from home Full-time role