Senior/ Biotechnologist (1-year contract)

Site Name: Singapore - Tuas Posted Date: Nov 19 2024 As a 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. Basic Qualifications NITEC/Diploma in chemical technology, chemical engineering or biotechnology engineering Min 2 years of experience in Biologics, Chemical or Pharmaceutical industry Experience in working with GMP Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations If you have the following characteristics, it would be a plus: 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. To learn more about Singapore GSK and our people, please click on this link: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore #Li-GSK Why GSK Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. 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