Quality Engineer

at  Abbott Laboratories

Central Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate08 Nov, 2024Not Specified09 Aug, 20242 year(s) or aboveJmp,Communication Skills,Fishbone,Data Analysis,Minitab,Gmp,Continuous ImprovementNoNo
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Description:

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

REQUIREMENTS:

  • Bachelor of Engineering or related discipline
  • Minimum 2 years of relevant experience in Quality Assurance
  • Good practical knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) in a food or pharmaceutical manufacturing industry.
  • Knowledge of problem-solving tools (e.g. 6M Analysis, Fishbone, 5 Whys, etc.).
  • Ability to do data analysis using Minitab, JMP is a plus.
  • Team player with initiative, drive, good communication skills and a strong command of written English.
  • Proven problem-solving capability, customer focus and commitment to continuous improvement.
  • Good report writing skills
  • Kindly note this position is based in Tuas
    Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity

Responsibilities:

  • Undertake plant events related investigations (pNC and NC)
  • Perform root cause analysis and identify corrective and preventive actions in addressing quality events
  • Monitor site CAPA and perform track and trending of monthly and quarterly events cause codes to
  • Support Monthly and Quarterly Quality Management Review (QMR) and Business Management Review (BMR)
  • Perform monthly updates to site quality metrics
  • Support site new product introduction activities (Deviations, FLTS documentation)
  • Perform Weekly, Monthly and Quarterly reporting as required for own business area
  • Review and approve event related rework protocols
  • Coordinates and support periodic plant stoppage activities and ensure line release in a timely manner
  • General knowledge of procedures and activities within own work area.
  • Applies research, information gathering and analytical skills.
  • Works under general direction, seeks assistance as needed.
  • Works with team to support achievement of project milestones and deliver on internal and/ or external commitments.
  • Contributes through quality and accuracy of own work.
  • Conveys information in a concise and professional manner.
  • Any other duties as assigned by supervisor.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Central Singapore, Singapore