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About Johnson & Johnson

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 in pharmaceutical, and medical devices and diagnostics markets Janssen 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 https://www.jnj.com/ .

1. Æ÷Áö¼Ç: Assoicate Analyst QC
2. °è¿­»ç: ¾á¼¾¹é½Å (Janssen Vaccines)
3. ±Ù¹«Áö: ÀÎõ ¼Ûµµ

4. ±Ù¹« ÇüÅÂ: Regular

[Responsibilities]

General Laboratory Activity

•      Compliance with laboratory safety requirements.

•      Compliance with laboratory-related regulations and requirements.

•      Preparation/Revision and review of GMP documents (Test method documents, Lab notes (Worksheet), Procedures)

•      Usage and Management of GMP documents / Assure that GMP documents are properly maintained and/or archived.

•      Internal and external audit/inspection Preparation and Response

•      Other laboratory Support activity (e.g., housekeeping)

QC Laboratory Test Activity (Main Tasks)

•      Perform QC tests (Release, Stability, and other tests) in compliance with GMP and corporate requirements/Procedures.

•      Writing and Review of analytical data.

•      Perform Lab investigation when an issue occurs.

•      Perform data integrity activity according to local regulations and JNJ internal.

•      Utilizes electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing.

QC Laboratory Management

•      Coordinate/Document/Handling non-conformances, corrective actions (CAPAs), and changes (change control management)

•      Improvement of lab practice

•      Perform maintenance for lab equipment.

•      Accompany visitors and provide training to visitors.

•      Manage and Review of GMP data in compliance with GMP and corporate requirements/Procedures.

•      Keeps supervisor informed of task status and issues.

•      Completes corrective and preventative actions (CAPA) as assigned.

[Requirements]

•      Minimum Bachelor's degree (in Chemistry, Chemical Engineering, Life Science, Pharmaceutical Engineering, or related fields)

•      Fluency in written English and conversational spoken English.

•      Interpersonal communication skills, persuasiveness, and an active desire to work with colleagues and external parties.

•      Good knowledge of the application of Microsoft Office programs. (Outlook, Excel, Word, and PowerPoint)

•      Demonstrated ability to organize and prioritize workload.

[Preferred Qualifications]

•      Experience in the pharmaceutical industrial experience in the QC department (analytical methods: product testing, raw material, chemical testing, method validation, bioassay).

•      Skilled in performing basic and some advanced testing within the functional laboratory is preferred.

•      Experience in performing independent troubleshooting & basic root cause analysis skills is preferred.

•      Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory is preferred.  Basic knowledge of compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC is helpful.

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[For more Johnson & Johnson]

- J&J Careers À¯Æ©ºê ä³Î : https://www.youtube.com/channel/UCZEsWOZwbcjcXHrgYq7sP4Q

- J&J Korea Facebook: https://www.facebook.com/JNJCareersKorea/

- J&J Linkedin: https://www.linkedin.com/company/johnson-&-johnson/

- J&J Corporate Page: http://www.jobkorea.co.kr/Company/1605233/Info

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www.careers.jnj.com