GlaxoSmithKline Services Unlimited Posted October 5, 2026

Digital and Technology Lead (MSAT)

Uk, United Kingdom Full time
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About this opportunity

The Manufacturing Science and Technology (MSAT) function at GSK’s Irvine manufacturing site provides technical expertise in the industrial application of science, innovative technology and process to ensure that Drug Substances and Drug Products are understood and their product performance is enhanced throughout their product life cycle.  MSAT entails all elements of the manufacture, testing and supply process.

Job Purpose:

The Digital and Technology Lead drives the adoption of industry recognised Digital and Technology solutions across the Irvine site to ensure optimum performance and automated-corrective responses are in place.  The aim is to ensure that technology is in place to measure process performance, provide deep data analysis and drive embedding solutions (including optimizing in-process controls).

This role encompasses the full manufacturing and supporting processes across the site (from simplifying technical transfer of Fermentation Strain - predictive scale-up - to highlighting purification performance improvements) through deep data analysis and leaning on process modelling to limit local experiments and simplify implementation of process change.  You will programme manage the implementation of technological solutions to drive process productivity and seek transformational change of established production processes.

Key Responsibilities (include..,):

•            Act as voice of the customer on behalf of MSAT using and re-using data and evolving knowledge, capturing requirements and needs for building Product data and knowledge

•            Provide a high level of technical expertise to site in the supply of data to support the standardisation, visualization, and improvement of business processes for Product Lifecycle Management including Continuous Process Verification, stability, validation, investigations, TRA, RCA, Product Performance Assessment (PPA), Continuous Improvement and Data Stewardship, as applied to manufacturing operations

•            Define the business processes and associated benefits for use of data, information and analytics. Link these to the site aims and escalate projects to fill any gaps

•            Keep up to date with technologies and capabilities that utilise data and information to ensure the appropriate solutions are utilised to maximise business benefits

•            Drive programmes of work for Fermentation productivity improvement by leveraging on latest technology and data capture/transfer

•            Identify digital solutions for data capture and analysis – e.g. equipment cleaning validation and positive confirmation of standards adhered to

•            Drive the use of digital by first intent through process modelling (e.g. mechanistic and empirical) and engage Global MSAT statistics and modelling teams for support

 

 

About You:

This role would suit a self-motivated person who has experience of working in a cross-functional, global supply organisation.  You will have strong people-management skills, including a proven ability to influence people to achieve goals (as y ou will work closely with a wide range of teams, colleagues, senior-stakeholders).  You will also have a strong continuous improvement mindset. Knowledge and previous interaction with Global MSAT and other support functions would be advantageous.

 

CLOSING DATE for applications:  Monday 19th of October 2026 (COB).

Basic Qualifications:

Relevant degree (eg; Scientific, Technical or Engineering) or strong relevant experience.

Relevant working experience in delivery of technical standards / solutions with proven application (eg; data-analysis and optimisation, or validation and change management, or product and process optimisation, process modelling, etc).

Evidence of managing improvement projects in a matrix environment

If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage Life at GSK | GSK .

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.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

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.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Uk, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3634 comparable Manufacturing & CMC roles across 172 biopharma companies.

3634Comparable roles tracked
3365Currently active
172Companies hiring similar roles
62Countries represented

Salary context

887 of 3634 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $123,600)

Where these roles are based

Top locations among the 3634 comparable roles

United States1680
Germany244
India165
France148
Ireland125
China118

+ 56 more countries

Seniority mix

1607 of 3634 peers have a known seniority level

Senior416
Manager366
Intern/Fellow/Postdoc243
Associate157
Principal132
Director116
Associate Director115
Senior Director53
Executive/VP9

Therapeutic area mix

26 of 3634 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease17
Oncology3
Rare Disease3
Respiratory1
Dermatology & Aesthetics1
Immunology1

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How we calculate "similar"

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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.