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** **Sr. QA Specilaist** **to be in** **Incheon.** **You will be responsible for** **:** + Provides quality support of production activities in accordance with J&J requirement (Experience of production or quality for Visual Inspection preferred) + Review and/or approve related documents (SOP, WI and other technical documents) + Review and/or approve Calibration and Qualification documents + Performs equipment release + Reviews and approves non-conformance investigations and CAPAs in compliance with GMP requirements and company procedures + Evaluates change proposals for impact and risk through change management/change control system and support coordination of cross-functional implementation plans. + QA oversight of production areas and systems + Supports audit / inspectional readiness activities to prepare the site for internal independent audits and health authority inspection + Conducts / supports training on decisions / conclusions of laboratory activities from quality point of view + Provide technical expertise regarding the interpretation and/or implementation of cGMP practices + Perform tasks in a manner consistent with the safety policies, quality systems, and FDA/EU/MFDS 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. + Up to 5-7 years of experience in a pharmaceutical industry, preferably in sterile manufacturing environment + Good verbal and written communication skills in English/Korean, facilitation, and presentation skills + Good technical writing skills + Strong organizational skills, including ability to follow tasks through to completion. Skills in prioritizing and meeting deadlines + Word processing, presentation, spreadsheet and database skills **Legal Entity** Janssen Vaccines **Job Type** Fixed Term **How to Apply** https://www.careers.jnj.com/ - Search position number “R-019991” - Apply **Application Documents** Free-form resume AND cover letter is required (in Korean or English). **Application Deadline** Open until the 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.