Quality Engineer
at Abbott Laboratories
Central Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 08 Nov, 2024 | Not Specified | 09 Aug, 2024 | 2 year(s) or above | Jmp,Communication Skills,Fishbone,Data Analysis,Minitab,Gmp,Continuous Improvement | No | No |
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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