JANSSEN VACCINES] MANUFACTURING PROCESS SPECIALIST (신입 지원 가능)

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.
nj.
om/.
1.
포지션.
Manufacturing Process Specialist, Operations 2.
계열사.
얀센백신 (Janssen Vaccines) 3.
근무지.
인천 송도 4.
근무 형태.
Regular [Summary] Manufacturing Process Specialist operates as an established support individual contributor that executes tasks that are typically routine, with some deviation from standard practice.
Provides support for internal teams in the Manufacturing Pharmaceutical Process Operations function.
Follows administrative processes to ensure accuracy, timeliness, and quality of deliverables.
Maintains high standards of professionalism, efficiency, personal communication, discretion, and independent judgment.
[Key responsibilities] Completes tasks for the support function of the Manufacturing Pharmaceutical Process Operations unit, and follows administrative processes to ensure accuracy, timeliness, and quality of deliverables Adheres to standard operating procedures to support initiatives, project plans, and key milestones related to the processing of ingredients and/or pharmaceutical products Helps with day-to-day activities and resources and escalates any concerns or issues to leaders to maximize successful business results Identify opportunities for improvement within the manufacturing process through trend analysis and continuous review of all operations Keeps record of process improvements to continually enhance program quality, cost, and scheduling Manages non-conformances to ensure timely investigation, root cause analysis and implementation of corrective and preventive actions Manages the manufacturing related aspects of the Change Control system in line with site procedures Maintains front-line knowledge of Good Manufacturing Practices (GMP) and regulatory issues to efficiently manage project tasks in accordance with internal and external regulations and procedures Demonstrates Johnson & Johnson’s Leadership Imperatives and Credo [Requirements] Minimum of Bachelor's degree or equivalent experience in chemical, pharmaceutical, bio-related major or equivalent Fresh graduates or 1~2 years of professional experience in related field Strong interpersonal and organizational skills Good communication / coordination skills along with multiple stakeholders Strong working knowledge of cGMP’s in a pharmaceutical manufacturing environment Fluent both in written and spoken English Be able to work a shift according to production schedule [지원 방법] www.
areers.
nj.
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om/company/johnson-&-johnson/ J&J Corporate Page.
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obkorea.
o.
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www.
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om #LI-SK2 Qualifications See above.