Skills: Manufacturing Engineering, QA / QC / Inspection
Education: Masters Degree
Employment Type: Full Time Contractor
Job Title: QO / QA Specialist
Duration: 7 months
Salary: Competitive Hourly Rate
Start Date: ASAP
My client is a world renowned Pharmaceutical manufacturer, and are currently working on a new project in Singapore.
They are seeking a QO / QA Specialist to join the team and assist with the project.
•Partner the manufacturing team in the implementation and adherence to the various quality systems and GMP requirements at the manufacturing suite.
•Partner the supporting business functions in the implementation and adherence of the various quality systems and GMP requirements.
•Support the manufacturing team with development and writing of process Standard Operating Procedures and Master Batch Records and ensure that it complies with current good documentation practices and the applicable global procedures and regulatory requirements. This includes approval of the associated revision.
•Provide quality oversight by reviewing and approving SOPs related to Manufacturing Support, Engineering, Manufacturing Sciences and Supply Chain to achive the site objectives for Takeda Singapore.
•Build strong partnership with all other departments to ensure open communication and acceptance.
•Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda's Code of Conduct.
Responsibility to adhere to any applicable EHS requirements.
If you know anyone who may be suited for this role, kindly refer them to me. We offer referral fees on successful placements.
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