Manufacturing Process Specialist

4주전에

Incheon, 대한민국 J&J Family of Companies 풀타임
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.
* 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 & Johnsons Leadership Imperatives and Credo

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 cGMPs in a pharmaceutical manufacturing environment
Fluent both in written and spoken English
Be able to work a shift according to production schedule

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