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대전 바이오 공장 신설 - QC Specialist (3년 이상, Chemical Lab / Micro Lab)

 

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.

 

 

 

바이오 공장 신설을 위한 각각의 Chemical LabMicro Lab의 design 및 운영을 담당해주실 QC Specialist를 모십니다.

포지션 지원시, Apply하고자 하는 Part (Chemical / Micro) 함께 기재하시어 지원을 부탁드립니다.

 

 

 

1. QC Specialist (Chemical Lab)

 

Your role:
 

  • Introduce the standardized equipment needed to build Quality Control Laboratory of new site and contribute to interpretation of results according to specialized test methods.
  • 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.
  • Responsible for re-qualification and maintenance for life cycle of lab equipment and ensure to perform standardized procedures such as daily check.
  • 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.
  • Responsible for preparing reagents, standards, and columns required for testing. Perform inventory and storage management to ensure smooth test operation.
  • Document validated test methods and other required analytical documents e.g. SOPs, work instruction based on understanding of GMP.
  • Contribute to problem solving associated with laboratory work such as OOT/OOS/DEV investigation.
  • Ensure that all laboratory operations maintain high level of safety, environmental protection and management and build systems that comply with the cGMP requirements of the relevant quality system.
  • Strictly comply with company EHS safety regulations and master skill of safety work and emergency rescue knowledge.
  • Take responsibilities in assigned projects as appropriate.
  • Actively report quality related events and participate in continuous quality improvement activities.
  • Overall performance of daily QC Specialist operations (chemical lab) in the new facility. 

 

 

 

 

Who you are:

 

  • Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, analytical chemistry, or a related discipline.
  • +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
  • Experience in introducing various chemical and biochemical test equipment and tech transfer.
  • Fluent in English. 
  • Team working

 

 

 

 

 

2. QC Specialist (Micro Lab)

 

Your role:

  • Participate in designing microbiology testing labs for new site, ensuring Quality Control environment that meets regulatory compliance standards.
  • Define user requirement specifications for QC equipment based on understanding of products and testing method. Conduct qualification of QC equipment and computerized system validation of QC systems.
  • Perform verification and validation of microbiological testing methods and collaborate on technology transfer from giving sites to ensure successful implementation of transferred technologies.
  • Ensure product quality based on deep understanding of microbiological testing techniques.
  • Responsible for qualification of clean room, and clean utilities, managing scheduling and resources.
  • Participate in aseptic process validation, cleaning validation and process validation.
  • Establish relevant analytical document (e.g., specifications, methods, logbooks) and local SOPs to comply with company standards.
  • Conduct microbiological testing-related education and training to strengthen the capabilities of the QC team.
  • Manage and maintain equipment and reagents required for microbiological testing.
  • Contribute to problem solving associated with laboratory work such as OOT/OOS/DEV investigation.
  • Ensure that all laboratory operations maintain high level of safety, environmental protection and management and build systems that comply with the cGMP requirements of the relevant quality system.
  • Take responsibilities in assigned projects as appropriate.

 

 

 

Who you are:

  • Minimum bachelor’s degree in pharmaceutical sciences, life sciences, biology, microbiology, or a related discipline.
  • + 3 years in the pharmaceutical, biotechnology or medical device in QC micro lab.
  • Experience in developing and maintaining QC micro systems and SOPs.
  • Good communication and collaboration skills with team members.
  • Flexibility and adaptability.
  • Fluent in English.

 

 

 

 

 

•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.)

•머크와 카카오톡 친구를 맺어 최신 채용 소식을 받아보세요! (상위 QR코드 클릭 혹은 링크 클릭:  http://pf.kakao.com/_wWuUb)


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!

 

Job Requisition ID:  281334
Location:  Daejeon
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

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The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Job Segment: QC, Pharmaceutical, Medical Device, Laboratory, Biotech, Quality, Science, Healthcare

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