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Pharmacovigilance QA Auditor Specialist

Johnson & Johnson

Raritan New Jersey United States of AmericaMidH-1B sponsor company
Sign in to applyVerified 1h ago
Location
Raritan New Jersey United States of America
Work model
On-Site
Level
Mid
H-1B history
2 approvals (FY2023)
Posted
Aug 17, 2026

About this role

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Quality & Compliance Audit Job Category: Professional All Job Posting Locations: Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for Pharmacovigilance QA Auditor Specialist to be located at Raritan, NJ; Titusville, NJ or Horsham, PA. As a Pharmacovigilance Quality Assurance Auditor Specialist you will be part of a dynamic global team working to enhance quality across the Company through pharmacovigilance audit and business partner collaboration. Are you interested in joining a team delivering outstanding results to our customers and patients? Apply now for this exciting opportunity!

Key Responsibilities

Leads the planning, conduct and reporting of routine PV internal and external audits Supports audits, data, internal facilities and processes in GxP/non-regulated areas Supports regulatory inspections in various supporting roles. Participates in projects or serves on teams, as assigned by supervisor. Provides consultation to business partners on routine tasks with occasional supervision. Collaborates with business partners when contacted for compliance inquiries and seeks advice on non-routine and more complex issues to ensure a departmental unified position. May assist in the preparation of training material if requested.

Qualifications

Education: Minimum Bachelor’s degree is required; Focused degree in a life, natural, or computer science is preferred. Experience and Skills: Required: A minimum of 4 years of relevant work experience in Pharmacovigilance Strong project management experience Strong verbal and written skills, including presentation skills Strong teamwork and collaboration skills Strong in data analysis, critical thinking and attention to details Experience working with Microsoft Office tools (Outlook, Power Point, Excel, Word) Preferred: Broad understanding of auditing process and landscape Audit experience in various audit types Other: This position requires 25% of domestic and/or international travel Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.  Johnson & Johnson is committed to providing an interview process that is

Listing verified 1h ago. Applications go through the company's official careers site.

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Pharmacovigilance QA Auditor Specialist at Johnson & Johnson, Raritan New Jersey United States of America | Yoinka