Responsibilities
· To manage QC samples (including receipt, storage and discard of samples).
· Control and audit of retain samples (process and raw materials).
· Coordination of Sample Logistics documentation and QC assay sheet issuance.
· Write, maintain, edit and review Standard Operating Procedures.
· Maintain data and records in compliance with regulatory requirements and Standard Operating Procedures.
· Manage and coordinate on-site/ off-site archival of QC documents.
· Perform stability pull samples according to stipulated time points.
· Actively contributes to operational efficiency/continuous improvement initiatives.
· Any other duties as assigned by your Supervisor/Manager.
Requirements
· Min Degree in Chemistry, Biochemistry, Biotechnology or Diploma in Chemistry, Biochemistry, Biotechnology.
• A minimum experience of 3-5 years in Pharmaceutical, Biopharmaceutical or related manufacturing environment.
• Six Sigma Greenbelt training would be helpful.
• Demonstrated experience e.g. in the area of method validation, method transfer, method verification, Unexpected Results investigation.
• Demonstrated ability to collaborate with cross functional or cross sites to achieve objectives.
If you are interested in any of the positions, do kindly drop your most updated resume to [email protected]
Esther Lim Suk Hui
R1872808
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599
