GlaxoSmithKline Services Unlimited Posted September 29, 2026

Lead Microbiologist

Uk, United Kingdom Full time
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GlaxoSmithKline Services Unlimited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

The Quality Assurance Department at the GSK Ware Pharma Supply Chain site is responsible for ensuring that all aspects of the manufacture of products is performed in a controlled manner and meets commitments to international regulatory bodies, as well as the requirements of current Good Manufacturing Practice.

The Microbiology Laboratory team works as part of the Site Value Streams to ensure that manufactured products are compliant and fit for purpose.  This includes product analysis, laboratory investigations, and trend analysis of microbiological results.

Job Purpose:

The purpose of the role is to perform analysis/collection of samples and support process or environmental monitoring (using a range of microbial/chemical techniques).  The Lead Microbiologist is skilled / proficient in Microbiological techniques (set up and use).  You will support the Laboratory Team Manager by providing expert laboratory analytical services for the site to ensure delivery of compliant products to our customers.  This includes trouble-shoot and identify remedial actions in line with procedure and working on specific initiatives aligned to Laboratory strategy.  You will work to assist the Laboratory Team Manager in overseeing the execution of batch/job testing and release (for testing groups), as well as providing guidance and support to the wider Microbiology team.

Key Responsibilities:

Prepare and check data accurately according to company, customer and regulatory requirements.

Verify the quality and accuracy of results for material to meet pre-defined acceptance criteria.

Take a lead role in the batch/job approval process.

Managing site Continuous Improvement (CI) and improvement initiatives.

Responsible for assigned items of Laboratory equipment and instrumentation or 5S standards (as an expert user, resolving issues and promoting best practice).

Take a lead role in provision of training for New Starters, and for Microbiologists in areas of expertise.

Responsible for the safety of self and others within the Laboratory.

Carry out testing using appropriate aseptic techniques.

About You:

This role would suit a motivated person who has strong experience of working in a GMP (Quality) environment.  Strong people skills and a proven ability to work in a team (eg; flexible approach, good communication, planning and organizational skills) as well as good report writing skills.   You should have knowledge/experience of microbiology laboratory testing techniques, ideally within a GMP environment (eg; knowledge of the microbiological requirements for non-sterile pharmaceutical manufacture).  An excellent understanding and appreciation of the testing of raw materials and final product, as well as environmental and water testing is important.  You will also have a strong continuous improvement mindset and a willingness to work towards standardised and lean working practices.

 

About Ware Manufacturing Site:

We are co-located with our R&D colleagues and recently opened a new, state-of-the-art oral solid dose facility at Ware.  At this location our scientists, technicians and engineers (from R&D and Global Supply Chain – GSC) work collaboratively together (using the latest technologies) to rapidly knowledge transfer and deliver GSK’s most innovative, medicines faster and more efficiently.  On site we produce over 60 million respiratory inhalers each year with growing demand in future years.  The site also processes Active Pharmaceutical Ingredient (API) for use both on site and other manufacturing sites in our network.

CLOSING DATE for applications:  Wednesday 14th of October May 2026 (COB).

 

Basic Qualifications:

Relevant qualifications and / or experience (laboratory / microbiological testing and experience of managing and planning day to day activities for a team)

Good understanding of key microbiological methodologies

Knowledge of current Good Manufacturing Practice (cGMP) and understanding of its impact on own role (and the implications of not following cGMP)

Preferred Qualifications:

Ability to perform microbial identification utilising Gram staining, biochemical techniques and full speciation using MALDI-TOF

Working with aseptic technique, and experience with laboratory investigations, CAPA, root-cause analysis tools and problem solving

Knowledgeable in the use of laboratory software, such as Sapphire/ LIFT and M-ERP

Document authoring ability / experience

Benefits:

GSK offers a range of benefits to its employees, which include, but are not limited to:

·       Competitive base Salary

·       Annual bonus based on company performance

·       Opportunities to partake in on-the-job training courses

·       Opportunities for support for professional development and chartership (accreditations and professional bodies)

·       Access to healthcare and wellbeing programmes

·       Employee recognition programmes

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

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.

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
Quality
Therapeutic area
Not listed
Location
Uk, United Kingdom
Employment type
Full time

How this role compares

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

We currently track 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 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
Lowest disclosed · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States350
Germany54
Ireland53
China53
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Respiratory1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

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.

40%
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Function Therapeutic area Seniority Country
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Regeneron UK Limited · Remote, United Kingdom · Manager
Function Therapeutic area Seniority Country
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.