Closing Date: 22nd January 2018

Roche Singapore Technical Operations Pte Ltd
Manufacturing Engineer I

Salary: 0.00

Key Responsibilities
  • Responsible for providing support to manufacturing operations by developing, coordinating and facilitating projects to ensure planned, predictable production operations in compliance with GMP regulations.
  • Lead and execute Continuous Process Improvements, CAPAs, CRs, and TAs in assigned area.
  • Align new improvement ideas according to site’s priorities and capacity.
  • Support inspection work such as presenting during inspections, responding to observations, and driving closure of inspection related Change Records.
  • Support Change Records Assessment and GMP documentation Review.
  • Participate in and lead project teams to deliver business results focused on improving manufacturing business processes to improve reliability, increase simplicity and enable growth.
  • Provide routine and ad hoc support for planning, coordinating, execution, and performance improvement of key manufacturing processes such as product change over.
  • Participate periodically in selected manufacturing floor activities to maintain up to date floor knowledge.

Who you are
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
Education and Experience
  • BS/BA in Science, Mechanical/Chemical Engineering or a relevant discipline.
  • Fundamental knowledge of Operational Excellence (Six Sigma, LEAN, 5S, etc) principles is a plus.
  • Minimum of 2 years of work experience in cGMP biopharmaceutical production, preferably including project management.
Knowledge, Skills and Abilities
  • Seeking candidates with an in-depth understanding of biopharmaceutical manufacturing process, strong analytical thinking and problem solving skills.
  • Demonstrated track record of taking initiative, resolving problems, recommending and implementing process improvement.
  • Must work collaboratively and effectively to foster effective interdepartmental and cross-functional partnerships.
  • Demonstrated ability to lead and drive improvement initiatives.
  • Excellent verbal and written communication skills. Attention to detail and quality oriented
  • Well versed in cGMP with the ability to ensure procedures, processes and systems are optimized and compliant.
  • Ability to work under pressure, assert oneself, fast decision making skills and high flexibility

Appointment to this position will be on local Singapore salary and benefits package.

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