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GSK

QC Specialist ASAT Trainee (Attach and Train Programme)

GSK is hiring a QC Specialist ASAT Trainee (Attach and Train Programme) in Singapore, Singapore. Level rates it ; you can apply on GSK.

Level's read on this job

  • Level rates this role Little AI ●○○○: aI is not part of the work.
  • The posting mentions Gmp Systems, quality control and biopharmaceutical manufacturing among its tools and skills.
  • Level classes it as an internship.
  • GSK has 947 other open roles on Level.

AI in this role

Participate in a 15-month biopharmaceutical manufacturing quality control trainee program with GSK.

Gmp Systems
quality-controlbiopharmaceutical-manufacturinglaboratory-techniquesanalytical-methods

The Attach and Train Programme (AnT) is a structured talent development programme designed to build a pipeline of skilled professionals for Singapore’s advanced biopharmaceutical manufacturing industry, supporting both current and future workforce needs.

As a trainee, you will go through a 15-month structured on-the-job training programme with GSK, gaining hands-on experience, industry-relevant skills, and mentorship from experienced professionals in a world-leading biopharmaceutical environment.

We welcome applications from both fresh graduates and mid-career individuals who are passionate about developing a career in the biopharmaceutical manufacturing sector.

Due to the nature of the programme and its eligibility requirements, we can only consider Singapore Citizens or Permanent Residents. For more information on this traineeship programme, please visit Career Conversion Programmes (CCP) for Individuals.


What will you learn:

  • Develop strong planning and organizing skills
  • Develop interpersonal skills and learn to work in a team
  • Understand the way of working in a GMP environment
  • Learn analytical methods and in-house reagents used in QC Laboratory
  • Develop technical understanding in reagent qualification and analytical method lifecycle.
  • To support data gathering for analytical method lifecycle/reagent lifecycle/masterdata management
  • To manage archival of GMP documents from analytical method lifecycle/reagent lifecycle/masterdata management
  • To support protocol and reports preparation for analytical method lifecycle/reagent lifecycle
  • To liaise with stakeholders in ASAT projects
  • To support reagent inventories and stability tracking management

What are we looking for?

  • Degree from an accredited college/university, preferably in Science discipline with a focus in pharmaceutical science/chemistry/biochemistry
  • Proficient in use of IT and software/systems
  • Knowledge of cGLP & cGMP
  • Common laboratory techniques
  • Laboratory experience in the pharmaceutical industry
  • Ability to quickly learn and apply GMP manufacturing requirements.
  • Strong written and oral communication skills
  • Deadline-driven, flexible with self-reliance to work in an empowered environment
  • Awareness and ability to work within culturally diverse teams
  • Strong drive for performance and attention to details
  • A keen interest in consumer healthcare science, product and development, and a passion for knowledge
  • Team player

What do we offer you?

  • Monthly training allowances (not subject to CPF contributions)
  • On-the-job training while working with a diversified team of professionals
  • Understand and experience the GSK Culture
  • Implement technical knowledge and skills that you have acquired
  • Apply and develop soft skills such as interpersonal, communications and negotiation skills
  • Transport to and from site to MRT stations in centralised locations all across Singapore

Where will I be based?

You will be based at one of our manufacturing site in Singapore Tuas.

Let’s do this!

You’ll find hints, tips and guidance on our recruitment process on our website –

Learn more about the application process | GSK
You can learn more about GSK and our careers here https://www.gsk.com/en-gb/careers/

Apply now!

Need help with your application?

Please email us at WW.EarlyCareers@gsk.com and let us know how we can help you.


Skills

Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

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. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

How we rate this

QC Specialist ASAT Trainee (Attach and Train Programme) at GSK rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Quality ControlBiopharmaceutical ManufacturingLaboratory TechniquesAnalytical MethodsGmp Systems

Questions you could be asked

  1. Tell me about a project where quality control was part of your work. What did you do?
  2. Tell me about a project where biopharmaceutical manufacturing was part of your work. What did you do?
  3. Tell me about a project where laboratory techniques was part of your work. What did you do?
  4. Tell me about a project where analytical methods was part of your work. What did you do?
  5. Walk me through how you've used Gmp Systems in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Quality Control, Biopharmaceutical Manufacturing, Laboratory Techniques, Analytical Methods, and Gmp Systems. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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