Up to $ mth bonus
Perm / Contract available
Good Culture + Benefits
Job Details
• Working hours: Office Hours
• Location: East
Job Descriptions
- Responsible for ensuring the laboratory operations in accordance to ISO 17025 and cGMP requirements
- Leads, designs and performs method development (i.e. bioassay and mycoplasma) and validation of new test procedures for incoming projects
- Functions as Technical Reviewer for A2LA accredited tests and non-accredited tests
- Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects
- Serves as subject matter expert (SME) in area of specialization, established standards for regulatory compliance
- Serves as technical liaison with Customers with regards to technical services and performs Customer site visits where required
- Participates in internal Quality Audits, System Audits, Audits conducted by external agencies and Regulatory Authorities
- Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements
Requirements
- Bachelor of Science or any related field; MSc. preferred but not essential
- Minimum 2-6 years of relevant QC microbiological experience working in an ISO17025 / GMP laboratory environment
- Experience in method validation and development, method transfer, qualification activities in regulated laboratory
- Good knowledge of ISO 17025, cGMP and other regulatory guidelines
- Good understanding/working knowledge of Project Management and Measurement Uncertainty (MU)
*Interested applicants, please apply with your resume with reason(s) for leaving previous employment(s), notice period, last drawn and expected salary.
All applications will be treated with strictest confidentiality.
We regret that only shortlisted candidates will be notified.
RecruitFirst Pte Ltd E.A. 13C6342
Joseph Yap Shi Hao (R