Analytical Science and Technology Leader

Analytical Science and Technology Leader

London Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead analytical strategies for key GSK products and ensure project success globally.
  • Company: GSK is a global biopharma company focused on advancing health through science and technology.
  • Benefits: Enjoy a supportive culture, opportunities for growth, and the chance to make a real impact.
  • Why this job: Join a team that values innovation and collaboration while tackling global health challenges.
  • Qualifications: 15+ years in analytical method development; experience in biopharmaceuticals preferred.
  • Other info: GSK promotes an inclusive environment where everyone can thrive and grow.

The predicted salary is between 43200 - 72000 £ per year.

This role is responsible for the leadership on all the analytical aspects of product lifecycle (PPQ/Commercial) for key GSK products and supports delivery of business-critical projects globally. The ASTL is accountable for one or more key GSK products. The ASTL has ownership for the end to end Analytical Product Strategy taking accountability from the R&D Analytical Leader at Process Performance and Qualification (PPQ) stage. The role is responsible for leading and defining comparability studies and suitable characterization strategies to support post approval changes.

Key Responsibilities

  • To provide technical analytical leadership for programs, projects and activities related to the specific product/s under the ASTL accountability to ensure business priorities and targets are met eg. NPI, product transfers, change management, regulatory submissions.
  • To be accountable for the Analytical Product strategy (APS). Maintenance and update of the APS through the post-approval product lifecycle eg. recommending specification and stability strategies, recommending novel analytical technologies based on product needs. Ensure that analytical methods developed by R&D are robust with respect to product lifecycle, focusing on the highest risk / most complex methods.
  • To lead and define comparability studies and suitable characterization strategies to support post approval changes for the accountable product/s. To compile and recommend acceptance criteria for release and stability tests to feed into the comparability strategies around TT process, change scale, material change. To provide analytical input and expertise into comparability protocols and summary reports for regulatory changes/documents and ensure Q&A follow-up during submission process.
  • To partner with teams across the business in a matrix-fashion in order to meet asset analytical needs, and to identify and mitigate analytical risks i.e. with R&D Analytical, PCS (site and central), Technical (site and central), Regulatory.
  • To ensure that the analytical method knowledge is embedded in the onward Technical Transfer to other GSK sites and to external sites.
  • To drive PAT (Product Attribute Testing) and new technologies for analytical testing related to the Product control strategy.
  • To support sites by providing leadership and expertise for analytical aspects of root cause analysis investigations (RCA) in the frame of complex investigations related to the accountable product.
  • To defend APS for the accountable product/s during HA inspections.

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • BS 15+ years' Experience with analytical method development, validation and transfer.
  • Experience in the biopharmaceutical industry with relevant experience in late stage product, CQA assessment.
  • Strong understanding of drug substance and drug product dose forms manufacturing disciplines and relationship of analytical testing and control strategy.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Ph.D. 10+ years' experience, MS 12+ years' Experience authoring regulatory files (IND, IMPD, BLA, MAA, etc.
  • Experience collaborating with third parties (CROs/CDMOs).
  • Knowledge of PLM (product lifecycle) key aspects: technical risk assessment (TRA), product performance qualification (PPQ) and continued process verification (CPV).
  • Knowledge and understanding of the statistics related to CPV, test method equivalence assessment, specification setting, stability studies evaluations, between others.
  • Knowledge of basic risk assessment tools as FMEA to apply to required risk assessments: TRAs, MRAs, E&L risks assessments.

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Why GSK?

Uniting science, technology and talent to get ahead of disease together. 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 organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology and oncology). 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.

Analytical Science and Technology Leader employer: Quality Control Specialist - Pest Control

GSK is an exceptional employer that fosters a culture of innovation and collaboration, making it an ideal place for professionals in the analytical science field. With a commitment to employee growth, GSK offers extensive development opportunities and a supportive environment where individuals can thrive while contributing to meaningful projects that impact global health. Located in vibrant regions such as Belgium and Italy, employees enjoy a dynamic work-life balance alongside competitive benefits and a focus on well-being.
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Contact Detail:

Quality Control Specialist - Pest Control Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Analytical Science and Technology Leader

✨Tip Number 1

Familiarise yourself with the latest trends in analytical science and technology, especially those relevant to biopharmaceuticals. This knowledge will help you engage in meaningful conversations during interviews and demonstrate your passion for the field.

✨Tip Number 2

Network with professionals in the industry, particularly those who work at GSK or similar companies. Attend conferences, webinars, or local meetups to build connections that could provide insights into the company culture and the specific role.

✨Tip Number 3

Prepare to discuss your experience with regulatory submissions and analytical method development in detail. Be ready to share specific examples of how you've contributed to product lifecycle management and risk assessments in previous roles.

✨Tip Number 4

Research GSK's recent projects and initiatives in analytical science. Understanding their current focus areas will allow you to tailor your discussions and show how your skills align with their strategic goals.

We think you need these skills to ace Analytical Science and Technology Leader

Analytical Method Development
Analytical Method Validation
Analytical Method Transfer
Biopharmaceutical Industry Experience
Late Stage Product Experience
Critical Quality Attribute (CQA) Assessment
Drug Substance and Drug Product Manufacturing Knowledge
Regulatory Submission Authoring (IND, IMPD, BLA, MAA)
Collaboration with Third Parties (CROs/CDMOs)
Product Lifecycle Management (PLM)
Technical Risk Assessment (TRA)
Product Performance Qualification (PPQ)
Continued Process Verification (CPV)
Statistical Analysis for CPV
Test Method Equivalence Assessment
Specification Setting
Stability Studies Evaluation
Risk Assessment Tools (FMEA)
Root Cause Analysis (RCA)
Product Attribute Testing (PAT)
Leadership and Team Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in analytical method development, validation, and transfer. Emphasise your background in the biopharmaceutical industry and any specific projects that align with the responsibilities of the Analytical Science and Technology Leader role.

Craft a Compelling Cover Letter: In your cover letter, express your passion for the role and how your skills align with GSK's mission. Mention specific experiences that demonstrate your leadership in analytical strategies and your ability to collaborate across teams.

Highlight Key Qualifications: Clearly outline your qualifications, especially if you have a Ph.D. or extensive experience in authoring regulatory files. Use bullet points to make these stand out, ensuring they are easy to read and directly related to the job description.

Showcase Problem-Solving Skills: Provide examples of how you've successfully led root cause analysis investigations or managed complex projects. This will demonstrate your analytical thinking and ability to drive solutions in challenging situations.

How to prepare for a job interview at Quality Control Specialist - Pest Control

✨Understand the Analytical Product Strategy

Make sure you have a solid grasp of the Analytical Product Strategy (APS) and how it relates to the product lifecycle. Be prepared to discuss how you would maintain and update the APS, especially in terms of stability strategies and analytical technologies.

✨Showcase Your Technical Leadership Skills

Highlight your experience in providing technical leadership for analytical methods and comparability studies. Be ready to share specific examples of how you've led projects or teams in the past, particularly in high-stakes environments.

✨Familiarise Yourself with Regulatory Submissions

Since this role involves defending the APS during health authority inspections, brush up on your knowledge of regulatory submissions like IND, IMPD, BLA, and MAA. Be prepared to discuss your experience in authoring these documents and how you ensure compliance.

✨Prepare for Cross-Functional Collaboration

This position requires working closely with various teams across the business. Think of examples where you've successfully collaborated in a matrix environment, and be ready to discuss how you identify and mitigate analytical risks with different stakeholders.

Analytical Science and Technology Leader
Quality Control Specialist - Pest Control
Location: London
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