Biotechnologist / Senior Biotechnologist

Tuas, Singapore

Job Description


Site Name: Singapore - Tuas
Posted Date: Jun 28 2022
Our Tuas site, one of only two GSK global vaccines manufacturing facilities worldwide, operates around-the-clock to manufacture the active ingredient used to make a GSK vaccine that protects children against pneumonia. As a Biotechnologist/Senior Biotechnologist in our Value Stream, you will participate in the preparation, operation and completion of assigned process stages to ensure the production of bulk drug substances is within establish timing and quality standards. You will also ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP, safety and environmental requirements. Key Responsibilities: Operations

  • 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 N+1
  • Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably
Planning
  • Follow the day-to-day planning
  • Assist Lead Biotechnologist or Shift Supervisor or Operations Superintendent in detailed team operations planning
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
Technology 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 other Department/Team
  • 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.
Why you? Basic Qualifications We are looking for professionals with these required skills to achieve our goals:
  • Must have NITEC/HIGHER NITEC/DIPLOMA in Biotechnology/Chemical Engineering/Life Science
  • Has relevant experience in Biologics/Chemical/Pharmaceutical/ Food or other regulated industry is preferred
  • Basic knowledge of cGMP
  • Familiar with purification and fermentation
  • A good team player and able to work independently
  • Good communication and documentation skills
  • Has disciplined and quality mindset
  • Comfortable to work in a cleanroom environment.
Why GSK
Uniting science, talent, and technology to get ahead of disease together
At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together.
  • Li-GSK
Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.
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Job Detail

  • Job Id
    JD1041810
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Tuas, Singapore
  • Education
    Not mentioned