Business Development Manager - Lab Automation

Lead Process Engineer - Medical Technology Manufacturing Scale-Up

South Wales (remote, with frequent travel to their manufacturing location in South/West Wales)

£50-60,000 base salary

An innovative medical technology company is entering an exciting new phase, transitioning from product development into manufacturing scale-up. With a groundbreaking product approaching commercialisation and production operations being expanded in South Wales, we are seeking a Lead Process Engineer to play a pivotal role in industrialising manufacturing and shaping the future of production.

This is a rare opportunity to join a growing business at a critical stage, taking ownership of process development, validation and production readiness while influencing how manufacturing evolves as the company scales.

The Role

As Lead Process Engineer, you will lead the establishment, optimisation and validation of manufacturing processes required to support product launch and ongoing production growth. Working closely with engineering and operations teams, you will help build robust, efficient and repeatable manufacturing systems capable of supporting commercial-scale production.

This role offers significant visibility, autonomy and the opportunity to make a lasting impact within an innovative and purpose-driven organisation.

Key Responsibilities

• Lead manufacturing process setup, optimisation and continuous improvement initiatives

• Support production transfer, process validation and manufacturing scale-up activities

• Develop and implement manufacturing procedures, work instructions and best practices

• Improve process capability, repeatability and production efficiency

• Support new product introduction (NPI), sustaining engineering and product lifecycle activities

• Collaborate across engineering, operations and manufacturing functions to ensure successful production growth

• Troubleshoot manufacturing challenges and drive practical, hands-on solutions

About You

We are interested in candidates from a variety of engineering backgrounds, including:

Process Engineer
Manufacturing Engineer
Manufacturing Process Engineer
NPI Engineer
Product Engineer
Production Validation Engineer

You'll ideally bring experience from a regulated manufacturing environment such as Medical Devices/Technology.

You will thrive in this role if you:

• Enjoy hands-on manufacturing and production challenges

• Have experience supporting process validation, technology transfer or production scale-up projects

• Are comfortable operating within a growing, fast-paced business

• Can balance immediate manufacturing priorities with longer-term operational improvements

• Enjoy taking ownership and driving projects through to completion

Location & Flexibility

• Home-based flexibility available

• Significant on-site presence required during manufacturing setup activities in West Wales

• Initial periods may involve intensive site-based support

• Travel and accommodation expenses supported

What's on Offer?

• Salary circa £60,000, depending on experience

• Opportunity to shape manufacturing strategy from an early stage

• Highly visible role with genuine ownership and influence

• Broad remit spanning process engineering, manufacturing, scale-up and lifecycle support

• Chance to help bring innovative medical technology products into commercial production

• Collaborative team environment with strong growth ambitions
  

Quality Engineer

Medical Technology Manufacturing Scale-Up

South Wales / Remote with Travel

£50-55,000 base salary

An innovative medical technology company is entering an exciting phase of growth as it establishes and scales manufacturing operations in South/West Wales. To support this transition, we are seeking a Quality Engineer to take ownership of manufacturing quality systems and become the key quality presence at the production facility.

This is a hands-on role with significant responsibility, offering the opportunity to build quality processes from the ground up and directly influence the successful scale-up of an exciting medical technology product.

The Role

As Quality Engineer, you will be responsible for developing and maintaining the quality systems, controls and processes that underpin manufacturing operations. Working closely with production, engineering and operations teams, you will ensure products are manufactured consistently, efficiently and in line with quality requirements.

You'll serve as the primary on-site quality lead, helping to establish robust manufacturing practices while supporting future production growth.

Key Responsibilities

• Own and continuously improve manufacturing quality processes and procedures

• Develop and maintain quality control systems across production operations

• Define and manage inspection, verification and acceptance criteria throughout manufacturing

• Oversee quality-related testing, fixtures, jigs and production controls

• Drive continuous improvement initiatives to enhance product quality and operational performance

• Support manufacturing scale-up activities and ongoing production performance

• Act as a technical quality interface for suppliers and support supplier quality activities when required

• Work closely with engineering and operations teams to resolve quality issues and implement corrective actions

About You

We are interested in candidates currently working in roles such as:

Quality Engineer
Manufacturing Quality Engineer
Production Quality Engineer
Supplier Quality Engineer
Quality Systems Engineer

You'll ideally bring experience from a regulated manufacturing environment, working on medical devices/technology.

The successful candidate will:

• Have strong experience within manufacturing quality environments

• Be comfortable working closely with production and operations teams

• Possess sufficient engineering understanding to engage with suppliers on technical specifications, tolerances and manufacturing requirements

• Enjoy taking ownership and driving quality improvements

• Thrive in a growing, fast-paced business environment

Location & Flexibility

Flexible home-based working arrangement
Regular travel to a manufacturing site in West Wales required
Increased on-site presence expected during manufacturing setup and scale-up activities
Travel and accommodation expenses supported

What's on Offer?

• Salary circa £50-55,000, depending on experience

• Opportunity to build and shape manufacturing quality systems from an early stage

• High level of autonomy, ownership and visibility

• Direct impact on production readiness and operational success

• Broad exposure across manufacturing, quality, supplier management and scale-up activities

• Chance to join an innovative technology business at a pivotal stage of growth

If you're a quality professional who enjoys building robust manufacturing systems, solving operational challenges and making a tangible impact within a growing organisation, we'd love to hear from you.

Production Technician

📍 Wimbledon, Surrey

🕒 Monday to Friday | 6:30am – 3:00pm

Are you an experienced Production professional looking for your next opportunity within a quality-focused manufacturing environment?

We are recruiting for a Production Operator to join a well-established and growing business in Wimbledon. This role would suit someone with previous experience working under GMP regulations who enjoys hands-on manufacturing work and takes pride in maintaining high standards of quality and compliance.

The Role

As part of the production team, you will play a key role in ensuring products are manufactured safely, efficiently, and in line with company procedures and quality requirements.

Key Duties

• Carry out production activities in accordance with GMP and company procedures

• Operate manufacturing and processing equipment safely and effectively

• Follow detailed work instructions and standard operating procedures (SOPs)

• Complete production documentation and batch records accurately

• Conduct routine weighing, mixing, packing, assembly, or processing tasks

• Maintain high standards of housekeeping, cleanliness, and workplace safety

• Support quality, compliance, and continuous improvement initiatives

About You

We are keen to speak with candidates who have:

• Previous experience within a production, assembly or manufacturing environment

• Exposure to industries such as pharmaceuticals, food production, cosmetics, medical devices, or chemicals

• Experience operating production or packaging machinery

• A reliable and positive attitude with good team-working skills

What's in It for You?

• Regular day shifts with no weekend working

• Stable Monday to Friday schedule

• Full training and ongoing development support

• Friendly, collaborative working environment

• Opportunity to join a growing manufacturing business

• Long-term career prospects within a regulated production setting

If you have manufacturing experience and are looking to join a company that values quality, teamwork, and continuous improvement, we'd love to hear from you.

Apply now to find out more.

Senior Medical Writer – Oncology

Are you an experienced Senior Medical Writer looking to use your oncology expertise to influence meaningful scientific communication, while enjoying flexible hybrid or remote working in the UK? This role offers the chance to take real ownership of impactful projects, shape publication and medical affairs programmes, and play a visible part in the growth of our client’s team.

About Our Client

Our client is an established medical communications agency with a strong track record of delivering scientifically robust, creative work for pharmaceutical and healthcare organisations. With offices in London and Manchester and well-structured remote and hybrid working options, they offer a supportive environment where experienced writers can contribute at a strategic level, collaborate closely with expert colleagues and see the impact of their work across a range of indications, with a particular focus on oncology.

The Opportunity

As Senior Medical Writer, you will be a key scientific voice within our client’s team, leading the development of clear, accurate and engaging content that translates complex data into compelling narratives for diverse audiences. You will contribute directly to medical affairs and publications programmes, working closely with account and scientific colleagues to ensure scientific integrity and strategic alignment.

What You’ll Be Doing

• Lead the planning, writing and review of high-quality medical communications and publications across oncology indications.

• Take ownership of key projects, ensuring scientific accuracy, clarity and alignment with client objectives and compliance requirements.

• Provide scientific leadership on accounts, contributing to strategic planning for medical affairs and publications programmes.

• Mentor and support junior writers, offering guidance on content development, scientific rigour and best practice in medical communications.

• Collaborate closely with client services, scientific and editorial colleagues to deliver cohesive, impactful programmes.

• Communicate complex scientific and clinical data in an accessible way for different audiences, including healthcare professionals and internal stakeholders.

What You’ll Bring

• Proven experience within a medical communications agency at Senior Medical Writer level.

• Strong scientific background with extensive knowledge and understanding of oncology; a PhD is advantageous.

• Experience delivering a variety of outputs across medical affairs and publications, such as manuscripts, abstracts, slide decks and other scientific materials.

• Superb leadership and communication skills, with the ability to guide projects and mentor colleagues confidently.

• In-depth knowledge of the pharmaceutical environment and how medical communications support wider clinical and commercial objectives.

What’s On Offer

Our client offers flexible hybrid and remote working options within the UK, enabling you to work from home or from their London or Manchester offices, depending on your preference. You will join a forward-thinking, collaborative and experienced team where your expertise is recognised and your input into strategy and delivery is valued. An excellent benefits package is available, alongside clear opportunities for professional development and progression.

How to Apply

If you are an established Senior Medical Writer with oncology experience and you are looking for a role where you can combine scientific depth with ownership, leadership and flexibility, we would be keen to hear from you. Please submit your CV to be considered for this position.

Clinical Lead

Permanent | Competitive salary

About Our Client

Our client is a well-established organisation operating in the clinical research and biotech space, partnering with sponsors on multi-regional studies. They are committed to gender equality and an inclusive work environment where everyone is treated fairly and with respect. Their culture supports flexibility, professional growth and a genuine focus on wellbeing, making it a strong setting for experienced clinical professionals who want to lead impactful work.

The Opportunity

This Clinical Lead position is a senior role with responsibility for providing direction and guidance to project teams across regions. You will coordinate site management and monitoring activities, and act as a key link between the project team and Project Manager, ensuring clinical operations run smoothly from start-up through to ongoing monitoring. It is an opportunity to use your expertise to influence study delivery while supporting and mentoring clinical teams.

Key Responsibilities

• Provide leadership, direction and guidance to the project team across multi-regional clinical studies.

• Coordinate site management and monitoring activities and communicate status updates to the Project Manager.

• Support and coordinate feasibility, site identification and site selection activities for multi-regional studies.

• Lead and assist with preparation of initial ethics and regulatory submission packages.

• Oversee approval processes and timelines to ensure studies progress as planned.

• Support the Project Manager with applications for Investigational Product (IP) and ancillary import/export permits and licences.

• Work with the Project Manager to coordinate initial IP shipment across regions.

• Lead internal CRA meetings and teleconferences, preparing sections of the agenda and following up on specific actions.

• Prepare agendas, meeting minutes and additional communication for internal meetings as required.

• Attend sponsor meetings and contribute to discussions, preparation of agendas and minutes as needed.

• Correspond directly with sponsors to provide information and updates where appropriate.

Minimum Qualifications & Experience

• Proven experience performing advanced clinical monitoring and site management tasks across multiple locations at a senior level.

• Demonstrated leadership skills with the ability to provide clear direction to clinical teams.

• Strong organisational skills and the ability to meet deadlines in a fast-paced, dynamic environment.

• Experience in coaching and mentoring clinical teams.

• Strong communication skills and fluency in verbal and written English.

Why Join Our Client’s Team?

• Work in an inclusive environment where diversity is welcomed and everyone is treated with respect.

• Access flexible working options to help balance professional and personal commitments.

• Benefit from paid parental leave for both parents and flexible leave entitlements.

• Take part in wellness initiatives that support your physical and mental wellbeing.

• Develop your career through ongoing development and training programmes.

• Contribute to meaningful clinical research and biotech projects with multi-regional impact.

How to Apply

If you meet the minimum qualifications and are ready to take on a senior leadership role in clinical research, we would like to hear from you. Please submit your application, outlining your relevant experience in advanced clinical monitoring, site management and team leadership.

Account Manager – Medical Communications – Hybrid

We are looking for an experienced Account Manager to take a central role in delivering high-quality healthcare communications across both medical affairs and publications. In this position, you will act as a trusted partner to clients, oversee projects from initial concept through to completion, and help shape the development of the wider team within a collaborative, hybrid working environment.

About Our Client

Our client is a dedicated healthcare communications agency working with organisations across the life sciences sector. They design and deliver strategic, evidence-led programmes that support better decision-making for healthcare professionals and improved outcomes for patients. You will be joining at a time of continued growth and demand for insightful, data-driven communication, with the opportunity to work on a diverse mix of projects. The team culture emphasises continuous learning, professional development, and working together to produce work that has a genuine impact.

The Role

As Account Manager, you will be responsible for managing day-to-day client relationships and ensuring that projects run smoothly across their full lifecycle. You will collaborate with senior colleagues to plan and deliver programmes, coordinate internal and external stakeholders, and provide clear, thoughtful guidance to clients. A key part of the role will be supporting and coaching junior team members, contributing to internal initiatives, and helping to strengthen the overall offering of the business.

Key Responsibilities

• Serve as the main point of contact for client accounts, building strong, long-term relationships and maintaining regular communication.

• Lead and coordinate projects across medical affairs and publications, from initial brief through planning, execution, and delivery.

• Work with senior colleagues to clarify objectives, shape strategy, and ensure projects are delivered to a high standard.

• Adapt your approach and communication style to suit different client expectations, therapeutic areas, and stakeholder groups.

• Facilitate effective information flow within the internal team to support smooth collaboration and timely delivery.

• Provide constructive feedback and day-to-day support to junior team members, helping them build skills and confidence.

Benefits

You will receive a competitive salary and a comprehensive benefits package designed to support your financial security, health, and work–life balance. This includes core benefits, flexible options, and access to wellbeing initiatives, alongside hybrid working and generous annual leave.

Why Apply?

This position is well suited to someone who enjoys owning client relationships, leading complex programmes in medical affairs and publications, and contributing to the growth of colleagues and the wider business. You will have the scope to influence project direction, the support of experienced senior team members, and the opportunity to develop your career within a flexible, supportive environment. If you’re ready to take the next step in healthcare communications, we encourage you to apply.