Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

QC Microbiology Supervisor

Leeds
4 days ago
Create job alert

Job Title: Lead Microbiologist/Team Leader

Vacancy type: Permanent, full time

Area: Leeds

Salary: Highly attractive basic salary along with annual bonus

SRG is working with a world class pharmaceutical company in Leeds. We are looking for an experienced microbiologist to lead the QC Microbiology team. This is a fantastic opportunity for an experienced microbiology leader to make a positive impact on this team. We are looking for an expert in PET (Preservative Efficacy Testing) within microbiology, along with great knowledge of microbiology testing within liquid pharmaceuticals.

Responsibilities include, but are not limited to:

Leads and coordinates all QC Microbiology testing and management activities to ensure compliance is maintained.
Supports all microbiology related activities for site activities to ensure data are generated and reported timely for pipeline growth.
Drives efficiency, performance and compliance to regulatory and business standards through effective planning and investigation of Quality events
Direct team members towards achieving daily and long-term business goals.
Effectively monitor and manage progress and performance and provide timely feedback to the relevant teams and team members.
Pro-actively lead operations and processes to ensure quality standards are met, e.g. GMP / GLP / H&S.
Drive compliance to MHRA, FDA, Regulatory and Company requirements / standards.
Leads team performance and objectives to ensure that the QC department achieve objectives on Quality, Cost, Safety, Delivery and Business goals / aims.
Coach, mentor and develop team members to encourage and support a high-performance work culture.
Co-ordinate testing plans to ensure that internal and external customer needs are met to agreed/required standards.

Skills Required:

BSc in Microbiology or an appropriately related discipline.
Ideal candidates should be an expert in analysis within a pharmaceutical environment under a cGMP quality system in a fast-paced environment, preferably with a strong working knowledge of how, TVC, TYMC, TAMC and PET (Preservative Efficacy Testing) analyses are performed.
Ability to provide and support rationale of preservation decisions to regulatory bodies.

The ideal candidate should demonstrate the willingness to develop within QC packaging as a long-term successor.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies.

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Related Jobs

View all jobs

R&D Manager

QC Packaging Technician

Analytical scientist(technology transfer)

Packaging Technologist

Laboratory Analyst

Senior Analyst

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.