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You will join our Life Sciences team in Singapore, supporting qualification and compliance activities within a pharmaceutical laboratory environment. This role focuses on microbial identification systems, ensuring equipment qualification, validation, and documentation are delivered in line with regulatory and project timelines. You will play a key role in driving continuous improvement and operational efficiency across QC lab processes.
Job Responsibility:
Drive and support QC equipment qualification activities in line with defined project timelines
Lead qualification lifecycle documentation and execution, including: URS, ERES, HLRA, Vendor & in-house IQ/OQ, PQ and Qualification Reports (QR)
Manage change control processes related to equipment qualification
Investigate and resolve qualification-related deviations and discrepancies
Collaborate with cross-functional stakeholders to ensure compliance and alignment
Ensure timely execution, review, and closure of qualification protocols
Support CAPEX-related activities within QC lab environments
Maintain compliance with HSE (Health, Safety, Environment) guidelines
Identify risks, propose mitigation plans, and participate in risk assessments
Contribute to continuous improvement initiatives in lab operations
Requirements:
Experience in pharmaceutical lab environments (QC / QA / Production), minimum 4 years
Experience in equipment qualification and validation
Academic background in Science, Biology, Microbiology, or related field
English proficiency
Nice to have:
Experience with microbiology lab systems (e.g. microbial identification systems) is a strong advantage
What we offer:
An international community bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)