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GSK

【今市】MSAT NPI/ Technologist

GSK is hiring a 【今市】MSAT NPI/ Technologist. Level rates it ; you can apply on GSK.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • Tools and skills the posting cites include M ERP, gmp and gdp.
  • Level classifies it as a mid-level role.
  • Level lists 942 other open roles at GSK.

AI in this role

Subject matter expert responsible for supporting product launches, transfers, and lifecycle changes through efficient project execution and process design.

M ERP
gmpgdpproject-managementrisk-managementprocess-optimization

Job Purpose:

The role serves as a subject matter expert responsible for supporting successful product launches, transfers, and lifecycle changes through efficient and effective project execution. Responsible for supporting Site Impact Assessments to assess the impact of proposed changes on the manufacturing site, as well as process design activities including data setup. This role provides in-depth technical expertise on specific technologies, equipment, and systems used in site manufacturing and packaging processes. The role supports efficient and compliant operations through advanced knowledge in system operation, validation, troubleshooting, and process optimization. The role also supports process improvements, root cause investigations, and technology transfers for new processes, equipment and/or technologies.

Key Responsibilities:

  • Provide subject matter expertise for site NPI processes to support successful product launches in compliance with applicable standards and regulations.
  • Support the development, maintenance, and continuous improvement of area-specific procedures.
  • Execute material management activities to create or modify materials within established timelines.
  • Support launch and transfer material maintenance activities to meet agreed milestones and delivery dates.
  • Contribute to the minimization of write-offs through NPI support and continuous improvement activities.
  • Support coordination across functions in the M-ERP Data Maintenance process.
  • Provide technical support for discontinuation of factory codes and related system updates.
  • Act as a subject matter expert for NPI and technical transfer activities.

*Future scope of job and working location will be determined by company.

Basic Qualification

Skill

  • Knowledge of GMP/GDP and good documentation practices, with experience supporting internal/external audits.
  • Strong technical expertise: proven ability to provide deep knowledge on manufacturing, packaging, systems, equipment, and process-related topics to support site operations, product launches, and technology transfers.
  • Cross-functional delivery and risk/project management: proven ability to work effectively across functions to support execution of complex projects, manage risks, and deliver activities within agreed timelines.
  • Results-oriented mindset and continuous improvement: committed to achieving business and quality objectives through strategic thinking, innovation, and a focus on continuous improvement. Drives operational excellence by identifying opportunities for optimization and delivering impactful technical solutions aligned with organizational goals.
  • Problem-solving and critical thinking: ability to analyze complex situations, identify practical solutions, and make informed decisions based on data and metrics.
  • Good understanding of advanced technology and smart manufacturing, including application of data science and digital tools.

Experience

  • At least 5 years of experience in pharmaceutical industries.

Education/certification/Language

  • Education: bachelor’s degree or equivalent in Scientific field (e.g. Pharmaceutical Chemistry and Technologies, Chemistry, Biology)
  • Fluent spoken and written both Japanese and English.

*Legal right to work in Japan.


Skills

CMC Strategy, Data-Driven Decision Making, Data Integrity, Debate Moderation, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Process Optimization, Project Leadership, Risk Awareness, Scientific Writing, Technology Transfer

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

【今市】MSAT NPI/ Technologist 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

GmpGdpProject ManagementRisk ManagementProcess OptimizationM ERP

Questions you could be asked

  1. Tell me about a project where gmp was part of your work. What did you do?
  2. Tell me about a project where gdp was part of your work. What did you do?
  3. Tell me about a project where project management was part of your work. What did you do?
  4. Tell me about a project where risk management was part of your work. What did you do?
  5. Tell me about a project where process optimization was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Gmp, Gdp, Project Management, Risk Management, and Process Optimization. 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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