[Quality] Safety Management Specialist-GVP [Heart Recovery]
Pharma
Job description
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: Customer/Commercial Quality Job Category: Professional All Job Posting Locations: Chuo-ku, Tokyo, Japan Job Description: Job Responsibilities: GVP staff is responsible for GVP activities including complaint handling and adverse event reporting to competent authority in Japan. He/she works at Tokyo Office closely and reports to Safety/GVP manager. Principle Duties and Responsibilities : Creating and submitting adverse event reports to PMDA. Handling and assessing complaints and safety issues Maintaining and updating Japanese IFUs and user manuals Controlling documents, procedures, and records related to GVP and post-market activities. Collaborating with product assurance and post-market engineering teams in the US headquarters. Obtaining complaint investigation results from the US headquarters and creating customer letters. Job Qualifications: Minimum 2 years of GVP and/or post-market engineering experience in the medical industries Good knowledge about GVP Ordinances and adverse event reporting Basic knowledge of Japan PMDA Act and QMS Ordinance English reading and writing skills (e.g., e-mail communication, translation of complaint information) Basic PC skills (Microsoft Excel, Word, PowerPoint, Access, Outlook) Preferred to have knowledge of cardiovascular related products Business level English communication skill Required Skills: Preferred Skills: Business Behavior, Compliance Management, Continuous Improvement, Data Analysis, Data Compilation, Detail-Oriented, Execution Focus, Goal Attainment, Internal Controls, Issue Escalation, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Report Writing
Stand out for this role
NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
DO NOT APPLY- TEST 1
Thermo Fisher Scientific — Carlsbad, California, USA
Mechanical Assembler
Thermo Fisher Scientific — Eindhoven, Netherlands
CRA (Level II)
Thermo Fisher Scientific — 2 Locations
Application Scientist
Thermo Fisher Scientific — Shanghai, China
DO NOT APPLY- TEST 4
Thermo Fisher Scientific — Remote, United States
Biostatistician II
Thermo Fisher Scientific — Beijing, China