IT Business Analysts

QC Analyst

Location: South London

We are partnered exclusively with a leading global brand within the healthcare industry, that has an exceptional and long-standing reputation.

As we move further in 2026, they are now underway with critical expansion projects focused on new manufacturing lines, upgrading equipment and expanding headcount across a number of operational teams.

As part of the expansion, the business is adding new headcount to their QC team at more junior and senior ends of the spectrum.

This new position will be required to be one of the more experienced members of the team. With an established track record in HPLC testing, troubleshooting and conducting out of specification investigations.

Career development and chances for progression in this company are genuine and if you are looking to develop your QC and analytical experience further, this could be the ideal opportunity.

For further details, please contact Mark Bux-Ryan or apply below.

Key experience:

Previous experience within QC testing, specifically with established HPLC testing
GC experience beneficial
GMP experience is essential
Experienced and ability to conduct investigations and manage out of specification investigations
Ability to support and guide more junior team members

QC, quality, control, analytical, science, scientists, laboratory, technician, good, manufacturing, GMP, HPLC, GC, chromatography, investigations, QA, assurance

Site Engineer

Location: Surrey, UK

Looking for an all round engineering role?

Want to mix maintenance and project work on a smaller, growing facility?

Look no further.

I am partnered exclusively with a long standing client who are expanding their engineering team with an “all rounder”. This will include maintenance within a manufacturing and facilities setting, as well as getting involved in project engineering, as the site undergoes change and development.

You will need to be hands on and willing to take on a variety of tasks in a fast paced and quick turnaround setting. Your ability to discuss GMP and GEP will be crucial as you bring an extra pair of experienced and willing hands to the company.

The role will be core hours (approx. 7am-3pm, with flexibility) working a 40 hour week. There will be an on-call rota that will include some Saturday working. Additional weekend hours and coming out on call will be paid additional.

Key experience:

Previous experience in a hands on engineering position within pharmaceuticals is essential
Experience of GMP is essential
The ability to discuss Good Engineering Practice
Multi-skilled engineering capability – both mechanical and electrical
Experience in engineering projects
An appreciation of IT and cloud based systems is advantageous
Experienced in both reactive and planned maintenance
Willig to be hands on and have a flexible approach to work

For further information, please contact Mark Bux-Ryan.

Engineering, manager, maintenance, electrical, mechanical, electro, mechatronics, planned, reactive, systems, controls, GMP, regulated, pharmaceutical, manufacturing, ISO, aerospace, food, chemical, quality, standards, GEP, automation, project, engineer

Senior Medical Writer – Join Our Client's Collaborative Team

Are you a seasoned Medical Writer with a passion for contributing to impactful clinical and regulatory projects? Our client is seeking a highly skilled and motivated Senior Medical Writer to be an essential part of their dynamic team. This is a permanent, full-time role suited for professionals with over 5 years of experience who thrive in an innovative and collaborative environment.

About the Role

As a Senior Medical Writer, you will play a client-facing role, working closely with medical monitors and senior leadership to develop high-quality medical and regulatory documentation. Your expertise and collaborative nature will help shape scientific narratives across multiple projects. This position gives you the opportunity to contribute to critical regulatory submissions, support strategic discussions, and make a meaningful impact within a supportive and professional organisation.

Key Responsibilities

• Prepare a range of regulatory documents, including Investigational New Drug (IND) applications, clinical study protocols, Investigator Brochures, and Clinical Study Reports.

• Develop and update critical documents such as IND Annual Reports, Development Safety Update Reports (DSURs), and Patient Informed Consent Forms.

• Collaborate across functions to provide guidance and support in the preparation and review of training guidelines, manuals, and similar documentation.

• Offer mentoring to new medical writers by providing constructive feedback, direction, and support.

• Engage directly with clients and cross-functional experts, managing timelines, coordinating reviews, and overseeing review meetings with professionalism and confidence.

What You Need

• Bachelor’s degree is required, and an advanced degree is preferred.

• At least 5 years of experience in a CRO or pharmaceutical environment, with at least 3 years in regulatory medical writing focusing on oncology.

• Proven ability as a lead writer for multiple document types, including Clinical Study Protocols, Investigator’s Brochures, DSURs, and IND applications.

• Experience collaborating with clients or sponsors, managing timelines, organising review cycles, and coordinating review meetings.

• Familiarity with electronic Common Technical Document (eCTD) modules and fast-track application processes such as INDs and BTDRs.

• Strong understanding of industry principles related to drug safety, regulatory guidelines, clinical trials, oncology, and pharmacology.

• Exceptional organisational skills with the ability to manage multiple priorities and projects simultaneously.

• Outstanding communication and interpersonal skills, alongside advanced proficiency in MS Office software.

What’s on Offer

Our client offers the opportunity to work remotely across the UK providing you with flexibility whilst being part of a collaborative and innovative team. This role combines professional development, visibility in critical projects, and the chance to directly impact meaningful clinical and regulatory initiatives.

About Our Client

Our client is a well-respected and innovative organisation dedicated to delivering high-quality medical and regulatory solutions. Their team operates in a supportive and professional environment that values collaboration and excellence. With extensive expertise and a client-focused approach, our client is at the forefront of clinical and regulatory writing, offering team members the opportunity to advance their skills and contribute meaningfully to projects that matter.

Apply Today

If you are ready to take the next step in your career as a Senior Medical Writer and join a forward-thinking organisation, we’d love to hear from you. Apply now and become part of an inspiring team that thrives on excellence and collaboration.

Join Our Client as an Associate Director in Healthcare Communications

Are you ready to take your career to the next level within the world of healthcare communications? Our client is seeking a motivated and experienced Associate Director to join their growing and collaborative team in London, United Kingdom. If you’re passionate about shaping impactful communications strategies in the healthcare sector and are eager to lead projects with purpose, this opportunity is tailor-made for you.

Why This Role Stands Out

Our client offers the chance to work on meaningful, high-impact projects that make a difference in people's lives. As an Associate Director, you’ll play a vital leadership role, driving client campaigns, guiding talented teams, and fostering innovation in a hybrid working environment designed to support flexibility and balance.

What You'll Achieve

• Shape and implement client communication strategies to address complex healthcare challenges effectively.

• Lead and inspire a multidisciplinary team to deliver exceptional results for client projects.

• Develop and nurture client relationships, serving as a trusted advisor and strategic partner.

• Collaborate with internal stakeholders to drive new business opportunities and company growth.

• Stay ahead of industry trends to ensure innovative and relevant communications solutions.

What We’re Looking For

• Proven experience in a senior role within healthcare communications, ideally as an Account Director or equivalent.

• Exceptional leadership and people management skills, with a focus on team development.

• Track record of delivering successful client campaigns and building strong client relationships.

• Excellent strategic thinking and problem-solving capabilities with a solution-oriented mindset.

• Strong understanding of the healthcare communications landscape, including regulatory considerations and industry trends.

Why Join Our Client’s Team?

• Be part of a supportive and inclusive culture that values innovation and collaboration.

• Thrive in a hybrid working environment, offering flexibility to balance professional and personal commitments.

• Contribute to meaningful projects that make a real difference in healthcare communications.

• Enjoy opportunities for professional growth and career advancement.

• Work alongside a passionate team of industry experts within a respected and forward-thinking organisation.

Your Next Move

If you're looking for a role where your expertise, creativity, and leadership can thrive while being part of a team shaping the future of healthcare communications, we’d love to hear from you. Apply now to join our client as their next Associate Director and make your mark in this influential field.

Territory Sales Manager - UK based (must be in/close to Oxford/Cambridge/London)

Role Overview

Are you ready to take the reins as a Territory Sales Manager, influencing key stakeholders and driving success in the Golden Triangle, UK? This exciting role offers the chance to collaborate with industry leaders, representing innovative solutions in Instrumentation & Laboratory Automation. If you’re passionate about building client relationships and delivering measurable growth, this is the opportunity you’ve been waiting for.

About Our Client

Our client is a forward-thinking organisation operating at the cutting edge of Laboratory Automation & Sample Management. With a focus on innovation and customer satisfaction, they empower their team to contribute meaningfully while working in a supportive and flexible environment.

About the Role

• Develop and manage strong client relationships to drive the adoption of advanced instrumentation solutions in laboratories.

• Identify key opportunities across the territory and implement tailored strategies to achieve measurable growth and market expansion.

• Collaborate with internal teams to provide client-focused services, ensuring satisfaction and long-term partnerships.

• Act as a trusted advisor to clients, demonstrating expertise in laboratory workflows and automation products.

Skills

• Experience in sales related to Life Science Instrumentation/Lab Automation/Sample Management, with a proven ability to engage and influence decision makers.

• Strong self-motivation for working autonomously in a remote capacity while meeting ambitious targets.

• Proven interpersonal skills to manage diverse stakeholders effectively within the scientific and laboratory sectors.

Next Steps

Ready to make a move? Submit your application today to explore this brilliant opportunity.

Role Overview

Are you a seasoned Cost Engineer ready to make an impact in the world of large-scale capital projects? Join our client’s team on a two-year contract and play a pivotal role in driving the financial success of their Global Engineering initiatives. With a focus on planning, execution, and financial control, this position is a unique opportunity to collaborate across dynamic teams and add value to highly regulated industries. This office-based role offers the chance to bring your analytical expertise to life in managing complex, high-stakes projects.

About Our Client

Our client is a global leader in operations and manufacturing, dedicated to engineering excellence and innovation within highly regulated environments. With a strong commitment to collaboration and best practices, they provide a platform where experienced professionals can contribute to challenging and impactful projects, all while developing their expertise in capital engineering solutions.

About the Role

• Develop and manage project cost estimates throughout all phases, from concept to closeout.

• Establish budgets, cost baselines, and accurate cash flow forecasts for multi-faceted projects.

• Monitor expenditures, analyze financial risks, and proactively address trends and variances.

• Collaborate with project managers, engineering, procurement, and finance teams to ensure seamless cost tracking and reporting.

• Prepare executive-level cost reports and dashboards to guide critical decision-making.

• Ensure compliance with industry standards, company policies, and financial controls.

• Drive continuous improvement through cost control procedures and benchmarking analysis.

Requirements / Experience

• Minimum 5+ years of cost engineering or project controls experience.

• Expertise in capital projects within regulated industries such as pharmaceutical or biotechnology.

• Proficiency in cost management tools like SAP, Primavera P6, EcoSys, or similar platforms.

• Advanced Microsoft Excel skills, including data analysis and reporting.

Skills

• Strong analytical abilities for accurate budgeting and forecasting.

• Collaborative approach to cross-functional teamwork.

• Effective communication skills to present financial data to key stakeholders.

• Technical proficiency in cost management systems to enhance project outcomes.

Next Steps

Ready to advance your career with a pivotal role in capital project engineering? Apply now and take the first step in joining our client’s exceptional team. We look forward to hearing from you!