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 https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Quality Assurance **Job Category:** Professional **All Job Posting Locations:** Incheon, Korea, Republic of **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** **QA Specialist** **to be in** **Incheon** **.** **You will be responsible for** **:** Data integrity + Provides quality support of GxP activities in accordance with J&J requirement. + DI & CSV document of laboratory/ execution system review (e.g., User Account Review, Backup & Restoration, Audit Trail Review, Archival and Retrieval, Periodic Review, Recipe Change Request) + Co-operate DI project with stakeholders + Provide active quality and compliance support and leadership to the site operational and quality units. Drive a culture of proactive quality and continuous improvement to ensure compliance with Johnson and Johnson standards, regulatory requirements and expectations. (e.g. health authority inspections and risk assessment, etc.) + Evaluate Change Controls through appropriate change impact assessments + Assists with conducting and developing site GMP trainings + Supports audit / inspectional readiness activities to prepare the site for internal independent audits and health authority inspection + Perform tasks in a manner consistent with the safety policies, quality systems, and MFDS/FDA/EU requirements **Qualifications / Requirements:** + A minimum of bachelor’s degree is required, in life sciences or related field, such as Biology, Chemistry, Microbiology, Engineering, Pharmacy, etc. + More than 1+ years of experience in a pharmaceutical industry including QA experiences, preferably in sterile manufacturing environment. **Legal Entity** Janssen Vaccines **Job Type** Fixed-term(1y) **How to Apply** https://www.careers.jnj.com/ - Search position number “R-028265” - Apply **Application Documents** Free-form resume AND cover letter is required (in Korean or English). **Application Deadline** Until position is filled **Notes** + Preference will be given to individuals subject to national veterans’ benefits and persons with disabilities upon submission of relevant documents as per applicable laws. + Only candidates who pass the resume screening will be notified individually. However, notifications may be delayed due to company circumstances. + If any false information is found in the application documents, the hiring may be canceled even after the offer is confirmed, and future applications may be restricted. + Submitted documents will not be returned and will be deleted upon request.