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TnP Trainee - QC Specialist (System and Support)
Career Conversion Programme for (Train-and Place with commitment to hire) Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a manpower development programme jointly supported by Workforce Singapore (WSG) and Temasek Polytechnic (TP).
The training programme consists of a 3-months structured facilitated training conducted by Temasek Polytechnic, followed by 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 website ([ Link removed ] )
A certificate will be given to successful trainees upon completion of the programme.
Purpose:
- To manage logistic activities within QC department
Key Responsibilities:
- Performs receipt and storage of sample in accordance to local procedure.
- Performs routine and non-routine sampling of raw materials and utilities with observation of GMP requirements
- Ensures proper packaging of samples and correct samples are shipped to offsite recipient timely
- Ensures a good inventory of QC materials (purchased and prepared materials/glassware) to support testings; ensures no over surplus of inventory
- Ensures wastes are disposed appropriately and promptly.
- Practices 6S and ensures good housekeeping of laboratory, work area and equipments.
- Supports equipment calibration and maintenance, performs autoclave requalification and washing machine verification
- Performs peer review for verification of task and data.
- Participates in laboratory investigation (when required) and assist in the timely closure investigations, CAPAs.
- Ensures proper archival of submitted document for easy retrieval
- Identifies and reports problems in QC to supervisor in a timely manner.
- Adheres to all safety and security policies and practises
- Manages ad-hoc support tasks
- Assist QC support manager in the management and operations of the team
- Scheduling day-to-day shopfloor activities and resources handling to ensure timely sample and material management Provides training to the team
- Provide guidance, support, and technical expertise to the team Involves in investigation and protocol and report writing (when required).
- Involves in SOP writing and updating.
- Organization and Management Responsibilities
- Creates strong team morale and a culture of accountability and ownership
- Provides leadership, guidance and technical expertise/support to the juniors
- Ensures continuous improvements of the QC operations
- Ensures expenditures are within budget
Skills:
Professional
- For QC Support Technologist - Fresh graduate of NITEC, Diploma in Science (or equivalent)
- For Senior QC Support Technologist Graduate of NITEC, Diploma in Science (or equivalent) with at least 4 years of experience/Degree holder with at least 2 years of working experience.
- For Lead QC Support Technologist Graduate of NITEC, Diploma in Science (or equivalent) with at least 8 years of experience/Degree holder with at least 4 years of working experience.
Technical
- Competent technical skills in good laboratory knowledge and hands on experience in inventory management
- Knowledge of cGLP & cGMP
Business
- For QC Support Technologist, Senior QC Support Technologist 1, 2
- Basic report writing skills (preferably with legible hanwriting)
- Basic planning and organizing skills (for individual time management and work planning) Good interpersonal skills
- Team player
- For Senior QC Support Technologist 3 and Lead
- Effective report writing skills
- Planning and organizing skills (for individual time management and work planning)
- Leadership and problem solving with analytical and logical thinking
Competencies:
- Effective report writing skills
- Planning and organization skills
- Able to work independently
- Team player
- Analytical skills with logical thinking
Where will I be based?
You will be based at one of our manufacturing site in Singapore near Tuas.
When can I start?
CCP Program starts in 5 Jul 2023, while the On the Job training start in Oct 2023.
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.
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.
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