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NoPosition TitleTypeYour RoleWho You Are
1Validation Specialist정규직1. The Validation specialist role will perform site qualification& validation and ensure that qualification& validation activities consistently comply with all regulatory and corporate requirements in support of regulatory requirements and customer expectations. 
 2. This position will also entail validation Management system operation and maintenance, to ensure the system compliance with all Domestic and Global regulatory and corporate requirements
 3. Develop site validation management procedures for equipment qualification, computerized system validation, process validation, cleaning validation, transportation verification, and HVAC/Clean Utilities ensure that site validation management procedure complies with regulatory requirements and global standards.		1. Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, or a related discipline.
 2. +5 years in the pharmaceutical, biotechnology in quality assurance, GMP compliance, operations, or Validation, ideally in a multinational company.
 3. Experience in developing CCS and APS/APV preferred.
 4. Experience in handling sterile product required.
2QC Specialist정규직1. Introduce the standardized equipment needed to build Quality Control Laboratory of new site and contribute to interpretation of results according to specialized test methods.
 2. Define User Requirement Specification (URS) of equipment needed to build laboratory, with sufficient understanding of product and testing methods, and conduct qualification to ensure that specialized laboratory equipment.
 3. Carry out analytical method validation and verification based on understanding of test method. Collaborate closely on analytical tech transfer from giving sites and contribute to resolve issues that arise during the implementation		1. Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, analytical chemistry, or a related discipline.
 2. A minimum experience of 3 years in the pharmaceutical, biotechnology or medical device in QC chemical lab(experience in biochemistry lab will add value) LIMS&SAP experience will add value
 3. Experience in introducing various chemical and biochemical test equipment and tech transfer.
3Automation Engineer
(Equipment related)		정규직1. Be responsible for automation function from design, installation till commissioning, qualification, start-up, and future plant operation
 2. Responsible of the implementation of site projects, leading or participating in them, contributing with your automation knowledge for the new Life Science Campus. Interact with cross-functional groups. 
 3. Responsible for the systems integration in the OT infrastructure, fostering IT/OT collaboration		1. Bachelor’s degree or above in Mechatronics, Automation/Electrical/Electronic  Engineering, IT, etc.
 2. + 5 years automation design/maintenance experience.
 3. Experience of working with PLC, HMI, PCS (Process Control System),  and DCS (Distributed Control Systems)
 4. Experience of working with SCADAs, Virtual Machines, Industrial Communications, Databases, etc. are preferred. 
4Automation Engineer
(WMS, ASRS related)		정규직1. Be responsible for supervising and optimizing the Warehouse Management System (WMS).
 2. Be responsible for systems integration in the OT infrastructure, fostering IT/OT collaboration.
 3. Collaborate with IT teams to communicating the WMS into other systems for data interface.
 4. Supervise and commissioning all facility package equipment system and material management package equipment system such as Automated Storage Retrieval Systems (ASRS).		1. Bachelor’s degree or above in Mechatronics, Automation/Electrical/Electronic  Engineering, IT, etc.
 2. + 5 years automation design/maintenance experience.
 3. Good technical skill of IT/OT infrastructure and package equipment system including networks, Active Directory, and backup & restore processes.
 4. Prefer to experience with WMS, Virtual Machines, Communication with other systems, and System validation, etc.
5Manufacturing Engineer정규직1. Act as manufacturing engineering lead, this position will be responsible for manufacturing equipment function from design, installation till commissioning, qualification, start-up, and future plant routine operation.
 2. Collaborate with cross-functional teams to design, develop, and implement manufacturing processes for the sterile manufacturing  product line.
 3. Conduct analysis and optimization of manufacturing workflows to improve efficiency, productivity, and product quality.
1. Bachelor’s degree in manufacturing engineering, Mechanical Engineering, Industrial Engineering  or a related field. 
 2. At least 5 years equipment design/maintenance experience regarding pharmaceutical equipment, biopharmaceutical process line, or medical device assembly line.
 3. Good experience and knowledge of typical equipment used for bag, bottle, syringe assembly and bag making process.
6Equipment Engineer정규직1. Responsible for process equipment function from design, installation till commissioning, qualification, start-up, and future plant routine operation
 2. Acquire necessary specifications and operations of process equipment from giving site via close communication, remote or on-site training		1. Bachelor’s degree or above in Mechanical, Electrical Engineering or related major
 2. At least 5 years process equipment design/maintenance experience regarding pharmaceutical equipment, biopharmaceutical process line, or medical device assembly line
7QC Manager (Bio, Sterility testing)정규직1. Build and develop site Quality Control organization of new site.
 2. Ensure QC employees are hired, trained, and qualified to support project execution.
 3. Establish QC management systems, procedures, and other required analytical documents.		1. A minimum total experience of 10 years 
 2. 5 years of supervisory position
 3. In the pharmaceutical, biotechnology or medical device in quality assurance, GMP compliance, operations or validation, 
 4. Multinational company experience
8Process Engineer정규직1. Act as process lead for new investment project in S. Korea for Life Science. The candidate will be responsible for process engineering function from design, construction till commissioning, qualification, start-up, and future plant routine operation. 1. Experience of Water For Injection Systems (MED & VCD)
 2. Experience of Pure Steam Generators
 3. Experience of Purified Water/EDI Systems
 4. Experience of Experience of Clean Compressed Air Systems
 5. Experience of Liquid Nitrogen Storage & Gas Carburetor
9Packaging Engineer정규직Manage and optimize packaging/labeling to ensure the output meets market demands, including tasks related to packaging localization and cost reduction projects1. Bachelor’s degree and above in engineering, materials, or related industrial major
 2. At least 5 years working experience in packaging and labeling design/development
 3. Project management skills preferred
 4. Good communication skills
10Production Planner정규직1. Responsible for the implementation of all SAP planning modules (mainly PP or MM module)
 2. Manage and execute production quantities and schedules for manufactured products, as well as coordinate packaging schedules for all products		1. Bachelor’s degree or above 
 2. 5+ years’ experience in the related areas
 3. SAP launch or at least user experience preferred
 4. Supply chain planning experience in a manufacturing environment preferred
11Production Head정규직1. Take overall responsibility of implementing and supervising site manufacturing activities, safety, quality, productivity, cost/budget control, customer service and new product introduction.
 2. Ensure related manufacturing objectives realization.		1. Bachelor`s degree or above, preferring material science and engineering, Pharmaceutical, or Biology. 
 2. 10+ years’ experience in manufacturing process and managerial role.
 3. SAP experience is a must.
12Tech Transfer Engineer정규직1. Responsible for transferring technology related to the CCM (dry-powder and liquid media), process liquid, sterile sampling systems, and filtration products during project phases (design, construction till commissioning.1. Bachelor`s degree in engineering, life sciences, or related field; advanced degree preferred
 2. + 3-5 years of experience in technology transfer within the biopharmaceutical industry
 3. Strong knowledge of GMP and regulatory requirements related to technology transfer