Career Conversion Programme

1 day ago


Singapore GLAXO WELLCOME MANUFACTURING PTE LTD Full time

Overview
The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand.
The training programme consists of 15 months of local attachment with GSK. Due to the nature of the programme, we can only consider Singapore Citizens and Singapore Permanent Residents. For more information, please visit Career Conversion Programmes (CCP) for Individuals
VS1
This position reports to the Production Superintendent and is an integral member of Production Shift Team. GSK is committed to an employee-orientated, high performance culture that emphasises process automation, quality compliance and continuous improvement.
Role Description:
To execute key process operations in accordance to established batch instructions and schedule to make APIs and intermediates as well as plant changeover
To learn Process and Workplace Safety and cGMP knowledge for manufacturing and to demonstrate understanding during execution
To identify opportunity for improvements and able to carry out short term improvement projects to achieve benefit
Inspects and maintains house-keeping of his assigned area for clean and safe working conditions as well as ensuring that personal protection equipment and safety equipment are maintained ready for use.
Perform plant trouble shooting using appropriate problem- solving tool to minimize plant stoppages and safety or quality incidents.
VS2
This position reports to the Shift Operations Superintendent and is an integral member of Operations Team. GSK is committed to an employee-orientated, high performance culture that emphasises process automation, quality compliance and continuous improvement.
Trainee will be trained to operate all API manufacturing related equipment and facilities in his assigned area in compliance with GMP and EHS requirements. Trainee to adhere to strict recording and filling of batch / manufacturing records, process safety and general housekeeping of all work areas. To provide practical processing inputs to identify opportunities for process improvement.
Trainee to be involved in:
Involve in hands-on execution of the plant operations and assist in trouble-shooting
Monitor and analyze processing parameters for atypical trends and improvement opportunities
Perform raw material dispensing and equipment configuration with additional logistical support responsibility
Prior experience with analytical instrument will be a plus point
Actively support continuous improvement initiative
Support quality or safety related investigation using appropriate problem-solving tool to determine the root causes and implement CAPA to prevent recurrence.
Support Quality & Safety audits
Adhere to any applicable EHS requirements
Ability to adhere to regulatory requirements, written procedures and safety guidelines
Ability to evaluate documentation/data according to company and regulatory guidelines
Ability to interact with inspectors (internal and external)
Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
Basic mathematical skills
Ability to organize work and handle multiple priorities and meet deadlines
Ability to understand, apply and evaluate basic chemistry and physical principles
Qualifications
VS1
ITE/ Diploma in Chemical Process/ Technology/ Engineering related
VS2
NTC/ITC/Diploma/Degree in Science or Engineering
What you will learn
VS1
Foundational on-the-job training experience working in cGMP and key Global Supply API manufacturing site with state of art manufacturing facilities, including first in class Continuous Manufacturing facility
To train to be an advocate for Continuous Improvement, with introductory basics on Lean Sigma concepts and coaching by supervisors to complete practical application through completion of improvement project
VS2
Demonstrate commitment to cGMP, EHS compliance aspects of pharmaceutical plant operation
Excellent self-motivated team player with hands-on attitude and good communication skills
Ability to understand, apply and evaluate basic chemistry and physical principles
Ability and willingness to work on 12-hour shift operations
This will be a 12-hours shift work.
Where will I be based?
You will be based at one of our manufacturing site in Singapore near Jurong.
How can I apply?
Applications are now open, please apply via this link:
We recommend you apply as soon as possible, because we accept ongoing applications and offer positions on a first come, first served basis
At GSK we value diversity and treat all candidates equally. We strive to make our recruitment process free of bias of any kind and aim to create an inclusive workplace at GSK. If you require any assistance, either to attend an interview or during the course of the recruitment process, please let us know
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