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

Apply Now

Analytical Technology Transfer Scientist

Macclesfield
1 day ago
Create job alert

Are you an experienced Analytical Scientist looking to make an impact in the pharmaceutical sector?

This is a fantastic opportunity for a driven and innovative scientist to take a leading role in supporting commercial drug products at our clients globally renowned pharmaceutical organisation at their state-of-the-art facility based in Macclesfield. You will ensure analytical performance, method robustness, and regulatory compliance across a portfolio of mainly Oral Solid Dose (OSD) medicines. You will be joining a high-performing team within a world-class pharmaceutical setting, where you'll contribute to high-impact commercial products with a global reach.

Key responsibilities:

  • Serve as the key point of contact for analytical testing of commercial drug products.

  • Support global manufacturing sites and CMOs with analytical expertise.

  • Collaborate across departments including Manufacturing, QA, QC, Regulatory Affairs, and External Sourcing.

  • Oversee method transfers, change control assessments, and market access projects.

  • Provide technical leadership on complex analytical investigations and lifecycle management.

  • Potential involvement in hands-on laboratory support and occasional international travel.

    About You

  • Degree, MSc or PhD in a Scientific field.

  • Strong industry experience in drug product analytical development and strong understanding of the life cycle of OSD, inhalation, or parenteral drug products—from late-stage development and launch through commercial production and post-launch management.

  • Working knowledge of SHE principles and cGMP compliance.

  • Proven ability to communicate and collaborate across cross-functional teams.

  • Exposure to Lean methodologies and multi-disciplinary CMC roles is a plus.

    Enjoy the benefits of a flexible hybrid working model while being part of a collaborative, forward-thinking environment that values innovation and excellence!

    Key words: Senior Analyst, Analyst, Scientist, Lab-based, Analytical Chemistry, Method Development, Method Validation, Method transfer, Method optimisation, HPLC, GC, chromatography, Oral Solid Dose (OSD), inhalation drug products, parenteral drug products, drug product lifecycle, stability testing, dissolution testing, cGMP compliance, lifecycle management, commercial manufacturing, global pharmaceutical, contract manufacturing organizations (CMOs), quality control (QC), CMC, Chemistry, Manufacturing, and Controls, process improvement, laboratory support, Macclesfield, Manchester, Stockport, Wilmslow, Knutsford, Altrincham, Congleton, Buxton, Stoke-on-Trent, Crewe, Sandbach, Northwich, Warrington, Nantwich, Chester, Liverpool, Glossop, Derbyshire, Cheshire, Greater Manchester, Staffordshire, VRS9087MP.

    Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Related Jobs

View all jobs

Analytical scientist(technology transfer)

R&D Scientist (Fixed-Term)

Senior Scientist

Instrument Manufacturing Engineer

Senior Optical Physicist - Medical Technology

Electronics Engineer

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.