[Innovative Medicine] CQ Specialist

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.

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

• Manage incoming inspection activities and sampling/in-country testing requests.
• Coordinate sample arrangement and retention sample management activities.
• Support batch release preparation by collecting and verifying required release documentation.
• Support redressing activities including documentation preparation and packaging component verification.
• Manage product destruction, write-off, and reconciliation activities.
• Support Product Quality Complaint (PQC) related warehouse activities.
• Ensure timely review and maintenance of warehouse quality documentation.
• Manage the Narcotics in strict compliance with applicable Korean regulations and J&J Procedures.
• Support warehouse inspections, audits, and Gemba activities.
• Collaborate with internal and 3PL partners to ensure compliance with J&J and GxP requirements.

• Bachelor’s degree in pharmacy, Life Science, Chemistry, Engineering, or equivalent.
• At least 2 years’ experience in pharmaceutical quality, warehouse operations, supply chain quality, or related areas.
• Understanding GMP/GDP requirements and pharmaceutical quality systems.
• Good communication skills in Korean, with working-level English for business communication.
• Strong technical aptitude is required(SAP, Tru-Vault, etc.).
• Ability to work independently and manage multiple priorities.

• Willingness to work at a warehouse on-site.
• Strong communication and stakeholder management skills.
• Knowledge of pharmaceutical distribution and warehouse quality processes is preferred.
• Work location: 이천 (경기도 이천시 마장면 프리미엄아울렛로 113-60)

#LI-Onsite

• 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.
• The documents submitted will not be returned and will be deleted upon request.