Pharmacovigilance QA Auditor Specialist

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 Pharmaco...