[Hanlim Pharmaceutical Co., Ltd.] 2026 Open Recruitment for New and Experienced Hires in the Development Department, Quality Assurance Department, Quality Management Department, Technical Support Department, Production Department, and Business Support Department

한림제약(주) · 경기 용인시 처인구 영문로 2-27

✨Job Description - Development Department: pharmaceutical planning and development strategy, preparation of regulatory documents such as CTD for pharmaceuticals, new drug approval and approval management, pharmaceutical license in/out - Quality Assurance Department (Head of Department): overall management of 3 QA teams, advanced GMP (cGMP) work, leading inspections by domestic and overseas regulatory authorities, QMS work such as deviations·changes·complaints - Quality Assurance Department: GMP work for aseptic lines, validation, change control, deviations and OOS, product specification documents, release management - Quality Control Department: physicochemical testing of products/raw materials, validation work - Technical Support Department: maintenance and preventive inspection of pharmaceutical production equipment, root-cause analysis and emergency response in case of equipment failure, improvement activities to enhance equipment performance and stability, inspection/calibration and history management of key measuring instruments, qualification assessment and documentation for production equipment, GMP-based equipment inspection, maintenance and audit response, spare parts management and maintenance planning - Production Department 2 (Manager): overall operation of the injectable manufacturing team, production planning and ERP operation management, QMS work, overall operation management of production equipment/facilities, leading stabilization and improvement of production processes, preventing production risks and responding to quality issues, managing on-site operations and organizational goals, collaborating with related departments and resolving issues, responding to regulatory inspections - Production Department 2: injectable product manufacturing, equipment operation·maintenance and qualification assessment, GMP and SOP compliance, production output and batch record management, workplace hygiene and production facility management, identifying on-site issues and improvement activities, performing URS/FAT/SAT for equipment purchases, responding to regulatory inspections - Production Department 3: tablet·capsule filling·coating production for solid dosage forms, maintenance of tablet presses·capsule filling machines, coating equipment maintenance - Production Department (contract): pharmaceutical manufacturing work - Business Support Department (health management contract): operation of the in-house health clinic, management of general/special health examinations, follow-up care for employees with findings based on health check results, statutory health manager duties, health education and emergency response measures, other common departmental tasks ✅Qualifications - No disqualification for overseas travel - Veterans/merit recipients are given preference in accordance with relevant laws - For men: completed military service or exempted - Development Department: bachelor’s degree or higher, major in medicine·pharmacy·chemical engineering·biotechnology·chemistry·life science or related fields in medicine/pharmacy/science and engineering, up to 10 years of relevant experience, fluent in English conversation - Quality Assurance Department (Head of Department): bachelor’s degree or higher, major in chemistry·microbiology·biotechnology·pharmacy or related fields, 13+ years of relevant experience (7+ years in QA), 5+ years of organizational management experience, experience with both sterile and non-sterile formulations, experience performing FDA(cGMP) PM - Quality Assurance Department: bachelor’s degree or higher (or expected graduation), major in chemistry or related fields, entry-level or 5 to under 10 years of relevant experience - Quality Control Department: bachelor’s degree or higher (or expected graduation), major in chemistry or related fields, entry-level or up to 5 years of pharmaceutical analysis experience - Technical Support Department: associate degree or higher, major in mechanical engineering·electrical engineering·electronics or related fields, 3+ years of maintenance experience for production equipment in a pharmaceutical company, understanding of GMP and equipment qualification work - Production Department 2 (Manager): bachelor’s degree or higher, 10+ years of injectable production experience, 2+ years of injectable manufacturing operation experience, experience in GMP documentation and manufacturing management, experience in team leadership and personnel management - Production Department 2: associate degree or higher, entry-level or 1+ year of vial injectable production experience, experience in GMP documentation and manufacturing management, computer literate, no color blindness/color weakness, corrected vision of 1.0 or higher - Production Department 3: high school graduate or higher, major in electrical/electronic engineering or equivalent practical experience, 5+ years of solid dosage form production experience, able to operate production equipment and perform basic root-cause analysis and initial response when equipment issues occur, experience analyzing causes of manufacturing process defects and quality issues and improving them - Production Department (contract): high school graduate or higher, no color blindness/color weakness, corrected vision of 1.0 or higher - Business Support Department (health management contract): associate degree or higher, nursing license required, contract period of about 1 year and 2 months 💖Preferred - Master’s degree or higher - Medical doctor/pharmacist license holders - Those with experience in cGMP and sterile formulations - Those with strong foreign language/computer skills - Those with relevant engineer or industrial engineer certifications - Those with PLC, electrical panel control, and automation equipment maintenance experience - Those with experience building a new plant - Those with experience in overseas regulatory authority inspections - Those with experience operating organizations for serious industrial accidents - Those fluent in English - Those with experience building injectable manufacturing/packaging lines - Those with experience in process improvement and innovation projects - Those with experience operating global-level GMP and manufacturing quality systems and responding to regulatory authority inspections - Those with experience operating/managing lyophilizers - Those with experience building new manufacturing lines - Those with process trouble-shooting experience - Those with experience in tablet pressing, capsule filling, and coating process operations - Those with strong computer skills - Those with relevant work experience 🏠Work Location - 2-27 Yeongmun-ro, Cheoin-gu, Yongin-si, Gyeonggi - Development Department work location: Headquarters (Seocho-gu, Seoul) - Quality Assurance Department work location: Plant (Cheoin-gu, Yongin-si) ⚡️Recruitment Process - 1st round: document screening - AI aptitude test - 2nd round: practical interview - 3rd round: executive interview 👉Application Period/Method - Application period: Friday, November 20, 2026, 23:50 (only applications received by then) - Application method: apply through the recruitment page 📋Other - For experienced candidates, a separate career description is required (free format) - For experienced candidates, separate negotiation possible - Year-end performance bonus paid separately - The AI aptitude test is only for applicants who pass document screening and have a bachelor’s degree or higher - Please refer to the website for the exact deadline - Successful applicants will be announced on the recruitment site and via text message after the deadline - Documents to prepare and attach: application form on the recruitment site, final school transcript, copies of certifications, career description (experienced candidates) - Contact: Recruitment QnA and HR team (02-3489-6142 / 6204)