Biotechnologist III

ABBVIE OPERATIONS SINGAPORE PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

ABBVIE OPERATIONS SINGAPORE PTE. LTD. is seeking a manufacturing professional to support cGMP operations for clinical and bulk drug substances. You will use systems like LIMS, SAP, and automated controls to execute and monitor production while maintaining batch documentation with high quality and efficiency.

The role requires adherence to SOPs, safety standards, and continuous improvement initiatives, with opportunities for training and development in a fast-paced production environment.

Qualifications

• Bachelor's Degree in Science, Engineering or equivalent.
• 2+ years of relevant experience in biologics production facilities.
• Proven problem-solving skills and ability to adapt to new requirements.
• Strong working knowledge of Microsoft and other software packages; SAP, LIMS, Atlas systems preferred.
• Experience with cGMP documentation and record maintenance preferred.
• Excellent teamwork, willingness to learn, and hands-on problem solving.

Responsibilities

• Adhere to cGMP and safety requirements.
• Ensure good housekeeping of production facilities for reliable operations.
• Identify areas for improvement and participate in CI projects.
• Participate in commissioning and qualification activities as required.
• Carry out duties as assigned by Lead or Supervisor.
• Provide guidance to new joiners and lead by example.

Skills

Problem-solving

Team player

Adaptability

Troubleshooting

Analytical skills

Education

Bachelor's Degree in Science or Engineering

Tools

SAP

LIMS

Atlas

Microsoft Office

Job description

Purpose

• Performs functions associated with cGMP manufacturing operations for the Manufacture of clinical and bulk drug substance per safety, regulatory and operational requirements
• Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) for executing and monitoring operations
• Complete batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.

Key Responsibilities

Operations & Technical

• Adhere to cGMP and safety requirements
• Ensure good housekeeping of associated production facilities so that they are kept in good operational order
• Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency
• Participate in commissioning and qualification activities as required
• Carry out other related duties as assigned by the Lead or Supervisor
• Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably

Training & Development

• Ensure that he/she is trained/qualified in the current effective SOP and OJT in accordance with the assigned training curricula prior to commencing operation.
• Proactively engage N+1 to discuss personal development and follow up on agreed development plan.
• To provide guidance and support to new joiner ensuring his/her smooth transition to the new environment
• To develop oneself as a process SME
• Guide junior employees to ensure knowledge transfer for business continuity.
• Conduct classroom and on-the-job (OJT) training as assigned.

Quality

• Comply with all relevant SOP/Batch record requirements.
• Perform timely review of documentation and make necessary corrections.
• Have good quality mindset and integrity to ensure products are manufactured with the highest quality
• Participate in deviation investigation process (Process, Environmental, Maintenance/Equipment, QC) and implementation of Corrective and Preventive Action (CAPA)
• Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements

Reporting & Documentation

• Operate key computer applications related to production function
• Ensure that batch record, checklist and logbooks are correctly recorded, cGMP complied and maintained
• Maintain clear communication with N+1 and fellow colleagues, providing clear feedback of any items pertaining to safety, quality and efficiency
• Participation in development and generation of production checklist, SOPs, validation protocols and the regular review and updates of these documents
• Perform VS review of completed documentation to ensure adherence to GDP
• To lead design/drafting of working instruction to ensure that it is user friendly to improve GDP

Technical Transfer

• Participate in new technology and/or new process transfer

Security/Safety/Environment

• Awareness and adherence to site safety procedure.
• Ensure safe operations on the field
• Identify and report all potential safety issues (personal protection requirement, equipment protection, way of working etc).
• Ensure proper housekeeping of assigned production areas to minimize safety hazards
• Participate in Safety Inspections
• Participate in Workplace Risk Assessment

Interface with cross-functional teams

• Coordination with department colleagues to ensure timely supplies of materials and buffers calibration/maintenance activities are supported.
• Open communication on sampling requirements to QC department
• Establish good working relationship with QA, QC, maintenance, calibration to ensure smooth operations.

Qualifications

• Bachelor's Degree in Science, Engineering or equivalent
• 2+ years of relevant experience working in Biologics Production facility
• Proven problem-solving skills and the ability to adapt to new requirements
• Strong working knowledge of Microsoft and other software packages, SAP, LIMS, Atlas systems preferred
• Experience with cGMP documentation and record maintenance preferred
• Excellent attitude towards work and keen willingness to learn and perform ‘hands-on’ work
• Excellent team player with strong troubleshooting and analytical skills
• Willingness and ability to perform shift work required