[상시채용] 바이오 공장 신설 프로젝트
Posted 19 Jun 2023
Daejeon, Daejeon - Republic of Korea
Req Id 264474
여러분만의 특별한 재능으로 머크와 함께 마법을 펼쳐보세요!
커리어 여정을 계속해서 탐험하고, 발견하고, 도전할 준비가 되셨나요? 커리어에 대한 열정으로 가득한 여러분처럼, 머크도 거대한 포부로 가득하답니다! 머크의 전 세계에 있는 구성원들은 과학 기술의 혁신으로 헬스케어, 생명과학, 그리고 전자소재 부문에서 사람들의 삶을 풍요롭게 만들고 있습니다. 머크의 구성원들은 한마음이 되어 고객, 환자, 인류, 더 나아가 지구의 지속 가능함을 위해 힘쓰고 있습니다. 그것이 바로 머크가 호기심 가득한 인재를 원하는 이유랍니다, 호기심은 모든 것을 상상할 수 있게 만드는 원동력이니까요.
머크 라이프 사이언스에서 한국에 바이오 의약품 소재 (Cell Culture Media) 공정 시설을 설립하게 되었습니다.
대전 둔곡지구에 설립될 바이오 공정 시설은 아시아태평양 지역의 제약 및 바이오 생태계를 지원하고, 바이오테크 및 제약 고객사들을 위한 제품 생산에 집중할 예정입니다.
대전 바이오 공장 신설 프로젝트 초기 단계부터 함께 이끌어가실 인재 분들을 모십니다.
Opened Positions
| No | Position Title | Type | Your Role | Who You Are |
| 1 | Equipment Engineer | 정규직 | 1. 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 |
| 2 | Production Planner | 정규직 | 1. 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 |
| 3 | Automation Engineer | 정규직 | 1. Responsible for EMS (Environmental Management System), BMS (Building Management System) and WMS (Warehouse Management System) functions. 2. Responsible for design and installation to commissioning, qualification, start-up, and future routine plant operation. | 1. Bachelor’s degree or above in Automation or other Engineering, Electrics, IT etc. 2. 5~10 years’ experience of automation design/project/maintenance. 3. Experience with EMS, BMS (Utility system and HVAC (Heating, Ventilating, and Air Conditioning) system), Package equipment’s SCADAs |
| 4 | Electrical Engineer | 정규직 | 1. Design, develop, and oversee electrical systems while ensuring environmental sustainability 2. Analyze data and make performance recommendations 3. Troubleshoot electrical issues to minimize downtime | 1. Bachelor’s degree or above in Electrics or other Engineering, IT, etc. 2. At least 5 to 15 years of experience in electrical design/maintenance |
| 5 | Tech Transfer Engineer | 정규직 | 1. 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 |
| 6 | Production Head | 정규직 | 1. 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. |
| 7 | QC Manager (Bio, Sterility testing) | 정규직 | 1. 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 |
| 8 | Site Quality Head (Bio,pharma - GMP) | 정규직 | 1. Build and develop site quality organization of new site. 2. Set up validation master plan for the project, ensure timely completion of facility/equipment/utilities qualification and process validation. 3. Design, establish and implement site quality management system. | 1. Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, chemical engineering, or a related discipline. 2. A minimum experience of 15 years, with 5 years of supervisory position, in the pharmaceutical, biotechnology or medical device in quality assurance, GMP compliance, operations or validation, ideally in a multinational company. |
| 9 | Process Engineer | 정규직 | 1. 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 |
| 10 | QA Manager (QMS) | 정규직 | 1. Ensuring compliance with all regulatory and corporate requirements in support of regulatory and customer expectations, by carrying out routine quality assurance and compliance tasks and activities. 2. Assist in the development, organization and execution of the company’s Quality Management system, ensuring product quality and compliance with all Domestic and Global regulatory and corporate requirements. | 1. Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, chemical engineering, or a related discipline. 2. A minimum experience of 10 years, with 5 years of supervisory position, in the pharmaceutical, biotechnology or medical device in quality assurance, GMP compliance, operations or validation, ideally in a multinational company. |
<유의사항>
•여러분이 찾고 계시는 채용 포지션이 없으신가요? 그렇다면 인재풀(클릭)에 여러분의 이력서를 등록해주세요! 향후 인력 수요가 있을 경우 최우선으로 안내드리겠습니다.
•지원 순으로 전형이 진행되며, 적합한 후보자 발견 시 채용이 바로 마감되오니 지원의사가 있으신 분들은 빠른 지원 바랍니다.
•서버 안정성을 위해, 인터넷 익스플로러가 아닌 구글크롬, 혹은 마이크로소프트 엣지를 통한 지원 바랍니다.
•보훈대상자 및 취업보호대상자는 관련법에 의거하여 우대합니다.
•지원서의 기재사항이 사실과 다른 것으로 확인되거나 Reference from previous employer 상에 채용상의 결격사유가 확인될 경우 합격 또는 채용이 취소될 수 있습니다.
•(The company reserves the right to withdraw the offer, it if discovers subsequently that a candidate has given false information in application or has provided false or fraudulent documentation in support of his/her application. The offer is conditional upon satisfactory results of reference checks.)
•"머크 코리아 채용" 카카오톡 페이지와 친구를 맺어 최신 채용 소식을 받아보세요! (카카오톡에 '머크 코리아 채용'검색 후 친구추가)
•머크 채용팀과의 커리어 챗에 참여하세요! 2024년 1/31~2/2, 3일간 진행되는 세미콘 코리아에서 진행됩니다. (자세한 내용 보기 : 클릭)
머크는 구성원들에게 아래와 같은 혜택을 제공하고 있습니다. 머크에서는 모두 호기심을 바탕으로 서로 다른 배경과 가치관, 그리고 경험을 가진 다양한 구성원들과 함께 성장할 수 있습니다. 머크는 다양성을 소중히 여기며, 이를 통해 탁월한 성과와 혁신을 이끌어내 과학 기술의 발전에 공헌하고 있습니다. 머크는 구성원 모두 본인만의 속도로 발전하고 성장할 수 있도록 커리어 개발의 기회를 제공합니다. 머크의 구성원들은 서로 돕는 건강한 기업 문화를 조성하고 있습니다. 머크에서 여러분만의 특별한 재능으로 인류의 진보를 실현하는 마법을 펼쳐보세요!
다양성으로 가득한 머크의 구성원이 되어주세요!
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The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
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