Biotechnologist - Singapore - GSK

    GSK
    GSK Singapore

    19 hours ago

    Full time
    Description

    Key Responsibilities

    Operations

    • Support setup and execution of manufacturing activities, including:
    • Preparation and supply of media, buffers, and materials
    • Manufacturing of intermediates and drug substances
    • Optimize utilization of manpower (Senior Biotechnologist) and process resources to maintain operational efficiency.
    • Adhere to cGMP and safety requirements.
    • Meet project milestones and deliverables, including:
    • Participate in commissioning and qualification activities
    • Support small equipment sourcing and material introduction
    • Collate process information to support detailed design
    • Design and draft operational documents, e.g., SOPs, checklists, OJT, and Workplace Risk Assessments (WRA)
    • Identify areas for improvement and participate in continuous improvement initiatives.
    • Perform other duties as assigned by N+1.
    • Senior Biotechnologist specific: Act as in-charge of process/operations areas to provide guidance and leadership, ensuring reliable process completion.

    Planning & Scheduling

    • Ensure adherence to project timelines.
    • Senior Biotechnologist specific: Assist Lead Biotechnologist / Shift Supervisor in detailed team operations planning.

    Training & Development

    • Complete training and qualification on current SOPs and OJT prior to commencing operations.
    • Engage proactively with N+1 for personal development.
    • Senior Biotechnologist specific:
    • Guide and support new joiners for smooth onboarding
    • Develop oneself as a process Subject Matter Expert (SME)
    • Provide knowledge transfer to junior employees for business continuity
    • Conduct classroom and On-The-Job (OJT) training

    Quality

    • Comply with IOQ, commissioning protocols, SOPs, and batch record requirements.
    • Review documentation and implement necessary corrections.
    • Maintain a quality mindset and integrity to ensure reliable equipment and process testing.
    • Participate in deviation investigations (Process, Environmental, Maintenance/Equipment, QC) and CAPA implementation.
    • Participate in cGMP self-inspections.

    Reporting & Documentation

    • Operate computer applications related to production equipment.
    • Ensure all documentation (IOQ, commissioning protocols) is accurate, cGMP-compliant, and maintained.
    • Maintain clear communication with N+1 and colleagues regarding safety, quality, and operational efficiency.
    • Participate in drafting and reviewing production checklists, SOPs, and validation protocols.
    • Perform verification and sign-off of documentation to ensure GDP compliance.
    • Senior Biotechnologist specific: Lead design and drafting of working instructions and SOPs to improve usability, clarity, and compliance.

    Technology Transfer

    • Participate in new technology and process transfer activities.

    Security, Safety & Environment

    • Follow site safety procedures and ensure safe field operations.
    • Identify and report potential safety hazards.
    • Maintain proper housekeeping in production areas.
    • Participate in safety inspections and Workplace Risk Assessments.

    Interface with Other Departments / Teams

    • Coordinate with colleagues to ensure timely supply of materials and buffers.
    • Support calibration and maintenance activities.
    • Communicate sampling requirements to QC teams.

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