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Tìm kiếm việc làm

Production Supervisor (Work location: VSIP 2 - Binh Duong)

  • Bình Dương
  • Trưởng nhóm / Giám sát
  • Lương thỏa thuận
  • Dược phẩm
  • 31/05/2017

Mô Tả Công Việc

  1. Coordinate all the activities in the establishment of Line, Labor, Material and Energy Standards.
  2. Communicate, guide and update subordinates on new policies, rules and regulations for understanding and implementation
  3. Ensure the safety and health of all personnel in operations and make necessary arrangements to address the welfare and well being of shift personnel
  4. Evaluate and recommend personnel who perform beyond their duty for recognition/ promotion
  5. Arrangement of personnel & assignment of daily work for every staff according to the delivery plan with approval by the Production Head. Ensure all staff about schedules in a timely manner.
  6. Analyse & recommend personel & machine or equipment need to Production Head to assure production activity with the good quality, low cost and delivery on time
  7. Assist and participate in the establishment of work system and procedures for effective and efficient manufacturing operation
  8. Ensure compliance to GMP, PIC/s regulations, policies and rules of UIP company and safety regulation in assignment area
  9. Find out RCA & CAPA for all findings of IQA, GMP audit, Corporate audit and close on time based on agreed leadtime. Ensure there are  no recurring findings.
  10. Enforce security and safety rules and regulations and conduct daily inspection of the manufacturing facilities.
  11. Consult and coordinate with Production Head, Production Scheduler and Frontline Process Leader on the daily and weekly activities of processing/packaging operation to assure delivery on time will full quantity, lowest cost, low bulk products inventory (reduce OT & 3rd shifts)
  12. Review Processing/ Packaging Batch Records for complete and accuracy and signs documents prior to submission to Production Head.
  13. Daily report on safety, utilization, yied, productivity, technical issues on Gemba daily meeting
  14. Report occurrence of any deviation or technical problem in processing operations to Production Head within 12h
  15. Investigate to find out the root causes and recommend necessary measures to prevent occurrence of the same incident
  16. Check and ensure that processing equipment and facilities are working under required operating conditions  and coordinates with Line Maintenance personnel regarding repair and maintenance issues.
  17. Maintain peace, order and harmony in the workplace.
  18. Participate actively Validation Team to make sure of applicability of Validated procedure Production
  19. Oversee and monitor Process validation batches
  20. Support and drive OE, 6S programs in assignment  production area.
  21. Support, consult  and recommend to Production Head optimal ways on budget, opex and improving cost.

Yêu Cầu Công Việc

Professional Background:

  • University graduate in Pharmacy or other related sciences
  • Can speak and write in English
  • Experience: At least 3 year experience in Pharmaceutical manufacturing operations

Competency Requirements

  • Decision Making. 
  • Work independently.
  • Problem solving skill.
  • Calm under pressure.
  • Responsible.
  • Good communication.

 

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