Sr. Manager, GCP/GVP

shionogi· Quality Assurance
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📍 Florham Park, NJ, USFULL TIME💰 USD 135K–165K

About this role

Overview

This role will support and maintain a robust GVP and GCP compliance program across the organization, with GVP QA as the primary responsibility and GCP QA as the secondary responsibility.

This role will collaborate with the Global GVP/GCP QA teams to provide quality oversight of pharmacovigilance (PV), business/licensing partners, distributors, clinical studies, CROs/vendors, ensuring regulatory compliance with FDA, EMA, PMDA, MHRA, ICH, additional local requirements as applicable, and other global guidelines.

Responsibilities

Responsibilities

  • Engage in the development, implementation, and maintenance of the GVP and GCP Quality Management System (QMS), ensuring compliance with worldwide and local PV regulations.
  • Actively engage in preparedness for the regulatory inspections, e.g., FDA PADE inspection. Collaborate with the Global QA teams in the development and execution of audit strategies, manage, oversee or conduct audits.
  • Ensure ongoing compliance with relevant GVP and GCP global and local regulatory requirements and guidelines, including management and support in maintenance of Pharmacovigilance System Master Files (PSMF).
  • Manage compliance with risk assessments, facilitate root cause analysis, and ensure the implementation and effectiveness of Corrective and Preventive Actions (CAPAs) and effectiveness checks.
  • Act as a primary GVP Quality contact of all GVP related matters and GCP Quality contact as assigned, collaborating with cross-functional teams and internal departments.
  • Drive the continuous improvement of GVP and GCP quality systems and procedures. 
  • Other duties as assigned.

Minimum Job Requirements

Qualifications

  • BA/BS in life sciences, a scientific, technical discipline, or a related field.
  • Minimum of 6 years of experience in a GVP/GCP QA/quality/compliance role or regulatory inspectorate role supporting PV and/or clinical study teams.
  • Working knowledge of GVP/GCP regulations and guidelines, including ICH, FDA, EMA, MHRA and PMDA requirements.

Competencies

  • Strong attention to detail, team player, agile, excellent communication skills, strong critical thinking skills, and effective problem-solving abilities.
  • Excellent project management, organizational, and leadership skills to manage cross-functional teams and multiple projects simultaneously. 
  • Capable of operating in an ambiguous environment.
  • Capable of operating independently with a leveled understanding of decision making.

Other Requirements

  • Ability and willingness to travel up to 15% of the year both domestically and internationally.
  • Must live a commutable distance to our US Corporate Headquarters in Florham Park, NJ. Hybrid office presence is required at 50% of the time per month.

Additional Information

The base salary range for this full-time position is $135,000 - $165,000. Individual pay is determined by several factors, which include but are not limited to: job-related skills, experience, and relevant education or training. The range does not include the comprehensive benefits, bonus, long-term incentive, applicable allowances, or any additional compensation that may be associated with this role. 

EEO

Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.

 

If you are qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling 973-307-3550 or by sending an email to ShionogiHR@shionogi.com.

Frequently Asked Questions

What is the salary for the Sr. Manager, GCP/GVP role at shionogi?
The listed salary for this Sr. Manager, GCP/GVP position at shionogi is USD 135K–165K. This is an FULL TIME role.
Where is the Sr. Manager, GCP/GVP position at shionogi located?
This Sr. Manager, GCP/GVP role at shionogi is based in Florham Park, NJ, US. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Sr. Manager, GCP/GVP role at shionogi full-time or part-time?
This is listed as a FULL TIME position. It is posted as a Sr. Manager, GCP/GVP role in the Quality Assurance department at shionogi.
Which team or department does the Sr. Manager, GCP/GVP at shionogi belong to?
This Sr. Manager, GCP/GVP position is part of the Quality Assurance department at shionogi. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Sr. Manager, GCP/GVP position at shionogi?
Click the "Apply Now" button on this page. You will be redirected to shionogi's official application portal hosted on icims where you can submit your application directly.
When was the Sr. Manager, GCP/GVP job at shionogi posted?
This Sr. Manager, GCP/GVP position at shionogi was posted on Oct 5, 2026. Apply as soon as possible — early applications are often reviewed first.
Sr. Manager, GCP/GVP
shionogi · 💰 USD 135K–165K
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You'll be redirected to shionogi's official application page on icims.