Perform OH stocks, Production Impact date, Last Time Buy analysis for EOL components.
Perform presentation to cross region, cross functional teams & route DR for approvals in Agile.
Review / update manufacturing working instruction / BOM in Agile system.
Work closely with Haemonetics R&D, Quality, Sourcing, RA and contract manufacturers to solve or de-risk manufacturing day to day challenges.
Able to document and report activities with appropriate amount of precision with data driven mentality.
Carryout any other duties and responsibilities as assigned by supervisor.
Requirements :
Bachelor's / master's degree of Mechanical, Biomedical, Chemical Engineering or equivalent.
Min 2-3 years working experiences in Manufacturing, Quality, Engineering or equivalent. Fresh Graduates are encouraged to apply.
Candidates who demonstrated experience and knowledge in one or more of the following areas will be given strong consideration :
Familiarity with the Agile system and related methodologies.
Proficiency in basic statistical tools, as well as experience with Six Sigma and LEAN manufacturing principles.
Experience in the development and / or production of Class I, II, or III medical devices.
Comprehensive understanding of medical device manufacturing standards, including but not limited to :
Good Manufacturing Practice (GMP)
Process Validation and Verification
Process Failure Mode and Effects Analysis (PFMEA)
Risk Management and development of Control Plans
Gauge Repeatability and Reproducibility (GR&R)
Design of Experiments (DOE)
First Article Inspection (FAI)
Preparation and execution of IQ / OQ / PQ protocols and reports
Statistical Process Control (SPC) and Process Capability Analysis
Application of Six Sigma methodologies for problem-solving
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Manufacturing Engineer • Butterworth, Pulau Pinang, Malaysia
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