Senior/ Operations Supervisor (HBV Product Transfer)

Posted:
5/2/2024, 5:00:00 PM

Location(s):
Singapore, Singapore

Experience Level(s):
Senior

Field(s):
Operations & Logistics

The Senior/ Operations Supervisor will support the set-up of the end-to-end production operations within the manufacturing facility so as to achieve productivity targets and objectives in a reliable, efficient and cost-effective manner, and meeting Quality and Health, Safety and Environment (HSE) regulations and other regulatory standards.

The Senior/ Operations Supervisor is a First Line Leader (FLL) serving the following key functions:

1. Management / Supervisory of the team of biotechnologist

  • Leading the team in completion of operation steps, delivery of batches and project deliverables

  • Provide guidance to the team of biotechnologists

  • Take sound technical decision with respect to process issues occurring on the shopfloor

2. First Line Technical Expertise

  • Provide technical expertise on the shopfloor to the team of biotechnologists

  • Assist in troubleshooting and investigation of issues that happened on the shopfloor

  • Ensure the development of technical competency of biotechnologists

  • To provide process and technical support in transferring operations and technology for Hepatitis B (HBV) drug substances product manufacture from current production site in Belgium RX59 to Singapore (SG) Tuas.

This role reports to the Operations Lead and will support him/her in any other tasks assigned.

Responsibilities

1. Operations Management

  • Responsible to support the set-up of the end-to-end production operations within the future manufacturing facility. Manufacturing activities include:

    - Preparation and Supply of media, buffers and materials

    - Manufacturing of intermediates and drug substance

  • Optimize the utilization of capacity and manufacturing resource with sustain efficiency in:

    - Facility

    - Manpower

    - Process

  • Adhere to cGMP and safety requirements

  • Meet project milestones and deliverables, e.g:

    Participate & Execute Commissioning and Qualification activities

    Small equipment sourcing and material introduction

    Collate process information to support process design

    Design and draft relevant document, e.g SOP, Checklist, OJT and WRA

  • Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency

  • Carry out other related duties as assigned by N+1

2. Planning / Schedule

  • Adherence to project timeline

3. Management

  • Ensure the morale, discipline and well being of the team are well managed and taken care of

  • Ensure timely intervention and escalation of any potential conflicts and misunderstanding between team members

  • Monitor, plan and coordinate resources to ensure effective utilization of operational staff

  • Conduct performance review and development discussion sessions to provide timely performance feedback to N-1 as well as supporting individuals in team to achieve career aspiration

  • Ensure team performance in delivering project deliverables

  • Ensure in place in use of GSK Production System (GPS), e.g Tier 1 board with KPI adherence, with the team

  • Ensure Capacity Management (CAPMAN), Continuous Improvement (CI), issues reporting and escalation, etc are in place in use for the team

  • Act as backup to run the process on the shopfloor when there are manpower shortages

4. Leadership (Senior Shift Supervisor)

  • Coach and provide guidance to the Shift Supervisor / biotechnologists in the production team in their execution of tasks

  • To assist the Operations Lead in ensuring the quality and delivery of tasks

5. Technology Transfer

  • Participate in new technology and / or new process transfer

6. Environment, Health, Safety and Wellness

  • Ensure safe and secure operations in the facility

  • Identify and resolve potential safety issues or risks together with the team

  • Support and facilitate safety audits and follow up on the recommendations and Corrective Actions (CAPA)

  • Responsible as the primary work permit approver for respective area

7. Training and Development

  • Ensure that all biotechnologists are trained in accordance to the training matrix

  • To provide support and guidance to new joiner, ensuring their smooth transition to the new environment

  • Develop oneself as process Subject Matter Expert (SME)

  • Guide junior employees to ensure knowledge transfer for business continuity

  • Assist in conducting on-the-job training of the team

8. Interface with Other Department / Team

  • Develop good relationship within the team and with other departments (including MSAT, QA, QC, TS, etc) to ensure timely delivery of objectives

Knowledge, Skills & Experience

  • DIPLOMA / DEGREE in any Engineering and Science related discipline

  • At least 10 years of experience in a pharmaceutical manufacturing plant as manufacturing technician or graduate with minimum 4 years of relevant working experience

  • Downstream purification and Chromatography experience

  • Basic knowledge of cGMP and Safety issue management

  • Knowledge in SAP transaction

  • Knowledge in biotechnology equipment

  • Good troubleshooting skills

  • People management skill

  • Effective communication skill

  • Effective organization skill

  • Continuous improvement mindset

  • Strong conflict management skill

To learn more about Singapore GSK and our people, please click on this link: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore 

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Glaxosmithkline Plc

Website: https://gsk.com/

Headquarter Location: London, England, United Kingdom

Employee Count: 10001+

Year Founded: 1929

IPO Status: Public

Last Funding Type: Grant

Industries: Biotechnology ⋅ Health Care ⋅ Pharmaceutical