TnP Trainee
7 months ago
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.
A certificate will be given to successful trainees upon completion of the programme.
Purpose:
To perform testing and support related activities in QC Biological team
Key Responsibilities:
Perform routine and adhoc/ non-routine testing in the following areas with good observation of GMP requirements:
Biological testings for raw materials release (All QA controlled materials). Biological testings refer to biochemistry and/ or microbiological testings. Biological testings for intermediates and product Biological testings for utilities (city water, purified water, water of injection, compressed gases, etc) Biological testings required to support manufacturing process validations and confirmations Perform routine environmental sampling in controlled environmental areasInitiate and participate in laboratory investigation (OOS / deviations / atypical results / invalid results) and assist in timely closure of the investigation and CAPA
Perform equipment calibration, maintenance and validation
Participate in method transfer / verification / validation
Participate in peer review for verification of task and data
Assist in SOP writing
Identify and report problems in QC to QC Superintendent in a timely manner
Practice 6S and ensure good housekeeping of laboratory, work area and equipment
Ensure good inventory of QC materials (purchased and prepared materials / glassware) to support testings; ensure no over surplus of inventory
Ensure wastes are disposed appropriately and promptly
Adheres to all safety and security policies and practices
Assist the Senior Superintendent/Superintendent in the management and operations of the team; may be indirectly responsible for a team of associates:
Scheduling day-to-day shopfloor activities and resources handling to ensure timely availability of test results Reviews test reports to ensure accuracy of test results in accordance with corporate, regulatory and external agency regulations. Provides training to the team. Provides guidance, support and technical expertise to the team. Involves in investigation and protocol writing (when required) Involves in SOP writing and updatingOrganization and Problem Solving:
Creates strong team morale and a culture of accountability and ownership Recommends and coordinates appropriate corrective actions to quality problems in conjunction with other teams/ departments Presents in timely manner major issues to the management with strategies on their resolution.Skills:
Professional
For QC Associate, fresh graduate in NITEC/ Diploma in Microbiology, Biotechnology, Life Sciences, Chemistry, Biochemistry
For Senior QC Associate, NITEC/Diploma in Microbiology, Biotechnology, Life Sciences, Chemistry, Biochemistry, with at least 2 years of working experiences or Fresh degree holder in Microbiology Biotechnology, Life Sciences, Chemistry, Biochemistry. Increased number of years of experiences are required for higher positions.
For Lead QC Associate, NITEC/Diploma in Microbiology, Biotechnology, Life Sciences, Chemistry, Biochemistry, with at least 8 years of working experiences or Degree holder in Microbiology, Biotechnology, Life Sciences, Chemistry, Biochemistry with at least 4 years of working experiences.
Technical
Competent technical skills in the following: Good laboratory knowledge and hands-on experience in chemistry testings o Laboratory equipment qualification (advantage) Knowledge of cGLP & cGMP (advantage)Business
Effective report writing skills
Planning and Organizing skills
Effective team player
Analytical skills with logical thinking
Good interpersonal skills
Leadership skills (advantage)
Competencies:
Good command of English
Good knowledge on usage of computers
Where will I be based?
You will be based at one of our manufacturing site in Singapore near Tuas.
How can I apply?
Why Us?
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 organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.
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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