What Jobs are available for Medical Assistants in Risca?

• Responsibilities : You will lead diverse Medical Communications projects within a skilled project team to deliver high-quality work to clients. Responsibilities include reviewing junior colleagues’ work for accuracy, and quality, as well as planning and overseeing projects
• Salary : £50,000 per annum
• Benefits : Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous holiday allowance, private medical insurance, critical illness cover, income protection, full funding for external training and more
• Role Type : Full-time, permanent
• Start Date :  We are currently recruiting for start dates throughout 2025 and 2026, including December and January, and you will be asked to state your availability on your application form
• Application Deadlines : Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role, or particular start dates, may close when suitable candidates are found
• Location : This role is available in our Global Headquarters in Cambridge , as well as our London , Manchester and Bristol offices

Do you have experience successfully delivering publications or medical affairs projects? Do you enjoy building and maintaining client relationships? Costello Medical are growing their team due to demand from both new and existing clients and are therefore looking for candidates with prior experience in medical communications who enjoy content delivery and project management to join us as Senior Analysts and Senior Medical Writers.

Senior Analysts and Senior Medical Writers take a leading role across projects and work alongside the teams to ensure that client deliverables are created to an exceptionally high standard, in line with agreed timelines. This involves providing strategic advice to clients at project initiation, supervision of the project team and regular interaction with clients. Senior Analysts and Senior Medical Writers are central to the quality control of a project, involving the review of colleagues’ work and the provision of constructive feedback.

Our Medical Communications sub-teams collaborate closely, which means you will have the opportunity to work across one, or both, of the following project types:

• Publications: Including strategic publication planning, poster design and production of manuscripts, abstract development, and more
• Medical Affairs: Including delivering advisory boards, creating medical information materials, providing congress support, organising medical education events, developing medical education materials, and more

You will play an integral role in supporting business development by cultivating and sustaining strong client relationships, as well as identifying opportunities to offer additional services within existing projects. As you advance in this position, you may be entrusted with increased responsibility for managing client relationships, preparing budgets and overseeing project finances, as well as acting as a line manager for interns within your team.

Hybrid Working Policy: We believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognise that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments.

Therefore, we offer flexible working arrangements that allow our colleagues who have passed probation to work from home up to half their time, measured across a 2-week rolling period. During your probationary period (normally the first 6 months of the role), you will be able to work from home 1 day per week.

Learn more about a typical day in the life of a Senior Analyst and Senior Medical Writer at Costello Medical:

Senior Analysts can progress to the Consultant role, and Senior Medical Writers to the Publication Manager position. Fast progression is available for high performers. As a Consultant or Publication Manager, you would have full responsibility for client management, including budgeting and business development, as well as project delivery. In addition, you would line manage team members and have internal responsibilities spanning areas such as recruitment and training.

To learn more about the tailored career progression we offer at Costello Medical, our colleagues share their experiences of growing with the company. Please click here to read more:

Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access, and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies, and charitable organisations. We have been listed in the Top 100 Best Companies to Work For list since 2017 and were proud to receive B Corporation accreditation in 2022. Learn more about us, our work, and our mission on our website:

Requirements

We are looking for individuals who are collaborative, self-motivated and enthusiastic with professional experience within an agency setting, of typically no less than two years. Specifically, we are looking for candidates with the following experience:

• Delivery of medical communications projects – either publications, medical affairs, or both
• Communicating directly with clients, including responding to different communication styles
• Day-to-day leadership of project teams, including delegating tasks and managing the time of others

Further essential requirements for the role are:

• A degree level qualification in a scientific discipline (minimum 2.1). We welcome applications from candidates with a diverse range of specialisms, including but not limited to; biology, chemistry, pharmacy and medicine
• Exceptional attention to detail and high degree of written accuracy
• Excellent proficiency in written English and arithmetic
• Strong scientific writing skills with the ability to tailor writing style to different audiences
• Project management skills sufficient to enable timely project delivery
• Excellent data presentation skills, including the ability to use Excel, PowerPoint and Word effectively and efficiently, to produce a professional, high standard of work
• Sufficient technical and strategic knowledge to provide clients with recommendations on project content and approach
• The capacity to maintain exceptional customer service and quality of deliverables under multiple competing demands
• The proven ability to build robust and sustainable client relationships
• The ability to motivate colleagues and take a leadership role in the delivery of project components

Benefits

Alongside our award-winning company culture, where every team member is celebrated, respected, and has their voice heard, we are proud to offer a comprehensive benefits package that includes:

• A starting salary of £50,000, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands to ensure a fair and consistent approach for all applicants, eliminating the need for individual negotiations
• 25 days’ annual leave plus bank and public holidays, as well as a holiday buy and sell scheme
• Flexible working hours and the chance to work from home for up to half of your working time after passing probation
• Flexible benefits scheme offering cash payments, additional pension contributions and more
• Private Medical Insurance which offers comprehensive cover on a “medical history disregard” basis
• Paid study leave and funding for external qualifications
• Critical Illness Cover, Income Protection and Life Assurance
• Paid and unpaid sabbaticals based on length of service

Learn more about our full reward package and the other benefits of working for Costello Medical:

You are required to submit your CV and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your CV should clearly state the dates of all qualifications and grades achieved where applicable.

Then, our recruitment process includes a telephone interview with a member of the Talent Acquisition team, followed by an assessment for you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation that you can prepare for in advance. Our standard recruitment process lasts around 4 weeks however, this can be adapted if necessary.

As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide:

Please note that, whilst we embrace AI to innovate and improve processes, your role may involve working with confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.

We can provide visa sponsorship for eligible candidates for our Senior Analyst and Senior Medical Writer role. You will be asked to provide details of your right to work in the UK within your application, however this will have no impact on the processing of your application.

For current Student visa holders looking to transition to a Graduate visa, in most cases you will be unable to join us in a permanent full-time position until you have submitted your Graduate visa application. Please refer to Immigration Rules - Immigration Rules: Appendix Student - Guidance - GOV.UK and Graduate visa: Overview - GOV.UK for more details. Please contact should you have any questions.

· Rare opportunity to break into medical sales

· Work within a growing sector

· Huge opportunity for personal growth and career progression

· Fully autonomous role - manage the accounts as your own business

THE ROLE: Thanks to a period of growth this company is looking for a new, highly motivated Sales Consultant to manage accounts and develop new business opportunities in northern England. You will sell a range of mobility equipment (such as wheelchairs and walking frames) and daily living aids to a variety of customers in the healthcare and care sector including hospitals, local authorities, care homes, and mobility stores. The expectation will be to visit customers for 3 - 4 days per week with the rest of the week strategically planning your approach.

THE COMPANY: This is the UK subsidiary of a US based organisation that has history going back 100 years and a worldwide presence. Their brands are market leaders in the US and are the preferred products of many customers. Now looking to replicate that success in the UK, this is an opportunity to build a business channel and progress your career as the division grows.

REQUIREMENTS:

· Field sales experience with strategic new business skills

· A motivated, proactive and confident person

· A considered and methodical approach to building pipeline

· Data analysis and strategic planning skills

· Full driving license and willingness to travel up to 80% of your week.

THE CULTURE: Despite being a large company globally, they have a "family feel" in the UK, they look after their people and attrition is very low. Very much an ethical, forward-thinking healthcare solutions provider.

The Package for Sales Consultant:

· Basic: £35,000 to £5,000 depending on experience

· Bonus: £ 000 - 12,000 per year

· Car allowance of £ 0 per month

· Benefits: Healthcare, pension, mobile, laptop, 25 days holiday + stats

The Sales Consultant role covers the South West of England and South Wales including: Bristol, Bath, Gloucester, Cheltenham, Cardiff, Newport, Taunton, Torquay.

• Advanced scientific degree (MD, PhD, PharmD, or equivalent) in a relevant life science discipline.
• Minimum of 3-5 years of experience as a Medical Science Liaison or in a similar field-based medical affairs role.
• In-depth knowledge of a specific therapeutic area (e.g., oncology, cardiology, neurology).
• Demonstrated ability to build and maintain relationships with Key Opinion Leaders (KOLs).
• Excellent presentation, communication, and interpersonal skills.
• Strong understanding of clinical trial design and data interpretation.
• Ability to travel extensively within the assigned territory and attend national/international conferences.
• Proficiency in medical literature review and scientific exchange.
• Understanding of pharmaceutical industry regulations and compliance guidelines.

• Establish and cultivate strong, peer-to-peer relationships with key opinion leaders (KOLs) and healthcare professionals (HCPs) in relevant therapeutic areas.
• Serve as a primary scientific and medical resource for internal and external stakeholders.
• Deliver scientific and clinical presentations on the company's products and research findings.
• Respond accurately and efficiently to unsolicited requests for medical information.
• Gather insights from KOLs and HCPs regarding disease state, treatment landscape, and unmet medical needs.
• Support clinical trial activities, including investigator identification and trial site support.
• Attend and participate in relevant medical congresses and scientific meetings.
• Provide feedback to internal teams on market insights, competitive intelligence, and scientific trends.
• Ensure compliance with all industry regulations, ethical guidelines, and company policies.
• Contribute to the development of scientific and medical communication strategies.

• Advanced scientific degree (Pharm.D., Ph.D., M.D., or equivalent) in a relevant life science or healthcare field.
• Significant experience as an MSL or in a similar medical affairs role within the pharmaceutical industry.
• Deep understanding of a specific therapeutic area (e.g., Oncology, Cardiology, Neurology).
• Exceptional scientific acumen and the ability to critically evaluate clinical data.
• Outstanding communication, presentation, and interpersonal skills.
• Proven ability to build and maintain strong professional relationships.
• Strong understanding of regulatory and compliance guidelines within the pharmaceutical industry.
• Ability to travel extensively and work independently.
• Proficiency in data analysis and interpretation.
• A strategic mindset and a proactive approach to problem-solving.

Test Engineer – Diagnostics / Medical Devices

Permanent, Full-Time

Based in Bristol

£ Competitive salary + Benefits

Are you a hands-on Engineer with a passion for testing and validating complex diagnostic systems?

Would you like to play a key role in developing next-generation molecular diagnostics with real-world clinical impact?

My client is a pioneering biotech organisation developing cutting-edge diagnostic technologies that combine machine learning, DNA sequencing, and advanced engineering to revolutionise the detection of disease. As part of their continued growth, they are looking to bring onboard a Test Engineer to support the integration, testing, and optimisation of highly specialised instrumentation within their R&D team.

Working in close collaboration with engineers and scientists across disciplines, you’ll contribute directly to the validation and verification of novel medical technologies - ensuring high performance, reliability, and compliance across every stage of product development.

Key Responsibilities of the Test Engineer – Diagnostics / Medical Devices will include:

• Testing complex instrument systems including electromechanical, software, thermal, and optical subsystems.
• Developing and optimising test protocols in collaboration with mechanical and manufacturing engineers.
• Providing technical insights and feedback from testing to guide design decisions and product improvements.
• Collaborating cross-functionally to drive verification and validation (V&V), troubleshooting and design control activities.
• Building, troubleshooting, and maintaining specialised instrumentation, including deployment and support at partner sites.
• Managing and delivering your own projects from concept through to completion.
• Supporting the implementation of ISO 13485 compliant quality processes.
• Drafting and maintaining detailed test documentation, procedures, and reports.

To be considered for the Test Engineer – Diagnostics / Medical Devices role, you’ll need:

• BEng / MEng / PhD in a relevant discipline (e.g. Engineering, Biomedical Engineering, Physics etc.) or equivalent working experience.
• Hands-on experience with testing and validation of complex systems e.g. combining fluidic, mechanical, optical, and thermal subsystems.
• Proven experience working on complex medical diagnostic systems or related electromechanical instruments.
• Proven ability to design and execute verification and validation (V&V) test plans and author associated SOPs.
• Skilled in interpreting technical drawings, circuit diagrams, and design documentation.
• Strong proficiency with CAD software (e.g. Fusion360, SolidWorks).
• Clear communication skills with the ability to present technical findings to varied stakeholders.
• Highly organised, self-driven, and adaptable to dynamic, fast-paced R&D environments.

Beneficial:

• Experience within the Medical Device, Biotechnology or Life Sciences sectors.
• Experience testing and maintaining early prototype stage systems.
• Experience developing products under Design Controls within an ISO 13485 or ISO 14971 compliant environment.

Whether you’re currently working in test and verification within MedTech or looking to step into a role with greater technical variety, this Bristol-based opportunity offers a chance to be part of a growing, mission-driven organisation creating life-saving diagnostic solutions.

For further information, please apply online or contact Katie-May Kress at CY Partners for further information.

Key Words: “Test Engineer, Validation Engineer, Systems Engineer, Instrumentation, Electromechanical, Diagnostics, Medical Devices, IVD, Biotech, V&V, Verification and Validation, ISO 13485, Design Controls, CAD, Fusion360, SolidWorks, Fluidics, Optical Systems, DNA Sequencing, Biosensing, Biotechnology, Bristol”

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

Field Service Engineer, Medical Systems

• Overall Earnings of £60,000 Including Overtime
• Overtime Paid Door-to-Door After 8 Hours Per Day
• Basic Salary £0,000 to 6,000
• Company Car / Van
• Overtime
• Commission
• Pension
• 25 Days Holiday Plus 8 Public Holidays
• Tablet and smartphone
• Fuel Card
• Life Assurance
• Private Medical Insurance

*** This is home-based field service role that will involve working ten hour days on a 4 day on, 4 day off rotation ***

The Role -  Field Service Engineer, Medical Systems

Following expansion this market leading company now seeks to recruit a technically motivated and customer focused Field Service Engineer, responsible for:

• Carrying out planned preventative maintenance, service and breakdown repair of medical systems
• Once fully trained, you will also provide after sales technical and commercial support
• Working within the healthcare market, you will be expected to offer the highest level of customer service, completing risk assessments, activity reports and other documentation required by this highly regulated sector

Your Background - Field Service Engineer, Medical Systems

Suitable candidates for this exciting role will need the demonstrate the following:

• NVQ, City & Guilds, ONC or higher in an Electrical or Electronics qualification
• A background working as a service engineer or a technical support engineer on electromechnical or electronics systems
• Any experience of sectors such as the following would be welcomed:
  -medical systems
  -laboratory equipment
  -biomedical equipment
  -water purification systems
  -pharmaceutical device
  -ex-forces engineering
  -electro-mechanical field service
  -water treatment equipment
  -electronics service
• A full UK driving licence

The Company - Field Service Engineer, Medical Systems

• Innovative leading supplier of healthcare solutions
• Trusted by both the private sector and the NHS to operate and maintain medical systems
• Their continued success is based upon an unrelenting commitment to research and development, world class facilities and the recruitment and retention of customer focused engineers
• Excellent manufacturer's training on state of the art medical systems
• Opportunity to develop your career within the healthcare engineering sector

This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or employment business.

Test Engineer – Diagnostics / Medical Devices

Permanent, Full-Time

Based in Bristol

£ Competitive salary + Benefits

Are you a hands-on Engineer with a passion for testing and validating complex diagnostic systems?

Would you like to play a key role in developing next-generation molecular diagnostics with real-world clinical impact?

My client is a pioneering biotech organisation developing cutting-edge diagnostic technologies that combine machine learning, DNA sequencing, and advanced engineering to revolutionise the detection of disease. As part of their continued growth, they are looking to bring onboard a Test Engineer to support the integration, testing, and optimisation of highly specialised instrumentation within their R&D team.

Working in close collaboration with engineers and scientists across disciplines, you’ll contribute directly to the validation and verification of novel medical technologies - ensuring high performance, reliability, and compliance across every stage of product development.

Key Responsibilities of the Test Engineer – Diagnostics / Medical Devices will include:

• Testing complex instrument systems including electromechanical, software, thermal, and optical subsystems.
• Developing and optimising test protocols in collaboration with mechanical and manufacturing engineers.
• Providing technical insights and feedback from testing to guide design decisions and product improvements.
• Collaborating cross-functionally to drive verification and validation (V&V), troubleshooting and design control activities.
• Building, troubleshooting, and maintaining specialised instrumentation, including deployment and support at partner sites.
• Managing and delivering your own projects from concept through to completion.
• Supporting the implementation of ISO 13485 compliant quality processes.
• Drafting and maintaining detailed test documentation, procedures, and reports.

To be considered for the Test Engineer – Diagnostics / Medical Devices role, you’ll need:

• BEng / MEng / PhD in a relevant discipline (e.g. Engineering, Biomedical Engineering, Physics etc.) or equivalent working experience.
• Hands-on experience with testing and validation of complex systems e.g. combining fluidic, mechanical, optical, and thermal subsystems.
• Proven experience working on complex medical diagnostic systems or related electromechanical instruments.
• Proven ability to design and execute verification and validation (V&V) test plans and author associated SOPs.
• Skilled in interpreting technical drawings, circuit diagrams, and design documentation.
• Strong proficiency with CAD software (e.g. Fusion360, SolidWorks).
• Clear communication skills with the ability to present technical findings to varied stakeholders.
• Highly organised, self-driven, and adaptable to dynamic, fast-paced R&D environments.

Beneficial:

• Experience within the Medical Device, Biotechnology or Life Sciences sectors.
• Experience testing and maintaining early prototype stage systems.
• Experience developing products under Design Controls within an ISO 13485 or ISO 14971 compliant environment.

Whether you’re currently working in test and verification within MedTech or looking to step into a role with greater technical variety, this Bristol-based opportunity offers a chance to be part of a growing, mission-driven organisation creating life-saving diagnostic solutions.

For further information, please apply online or contact Katie-May Kress at CY Partners for further information.

Key Words: “Test Engineer, Validation Engineer, Systems Engineer, Instrumentation, Electromechanical, Diagnostics, Medical Devices, IVD, Biotech, V&V, Verification and Validation, ISO 13485, Design Controls, CAD, Fusion360, SolidWorks, Fluidics, Optical Systems, DNA Sequencing, Biosensing, Biotechnology, Bristol”

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

Field Service Engineer, Medical Systems

• Overall Earnings of £60,000 Including Overtime
• Overtime Paid Door-to-Door After 8 Hours Per Day
• Basic Salary £0,000 to 6,000
• Company Car / Van
• Overtime
• Commission
• Pension
• 25 Days Holiday Plus 8 Public Holidays
• Tablet and smartphone
• Fuel Card
• Life Assurance
• Private Medical Insurance

*** This is home-based field service role that will involve working ten hour days on a 4 day on, 4 day off rotation ***

The Role -  Field Service Engineer, Medical Systems

Following expansion this market leading company now seeks to recruit a technically motivated and customer focused Field Service Engineer, responsible for:

• Carrying out planned preventative maintenance, service and breakdown repair of medical systems
• Once fully trained, you will also provide after sales technical and commercial support
• Working within the healthcare market, you will be expected to offer the highest level of customer service, completing risk assessments, activity reports and other documentation required by this highly regulated sector

Your Background - Field Service Engineer, Medical Systems

Suitable candidates for this exciting role will need the demonstrate the following:

• NVQ, City & Guilds, ONC or higher in an Electrical or Electronics qualification
• A background working as a service engineer or a technical support engineer on electromechnical or electronics systems
• Any experience of sectors such as the following would be welcomed:
  -medical systems
  -laboratory equipment
  -biomedical equipment
  -water purification systems
  -pharmaceutical device
  -ex-forces engineering
  -electro-mechanical field service
  -water treatment equipment
  -electronics service
• A full UK driving licence

The Company - Field Service Engineer, Medical Systems

• Innovative leading supplier of healthcare solutions
• Trusted by both the private sector and the NHS to operate and maintain medical systems
• Their continued success is based upon an unrelenting commitment to research and development, world class facilities and the recruitment and retention of customer focused engineers
• Excellent manufacturer's training on state of the art medical systems
• Opportunity to develop your career within the healthcare engineering sector

This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or employment business.

• Conduct thorough client consultations, assessing skin conditions and discussing treatment goals.
• Develop customized treatment plans utilizing a range of aesthetic modalities.
• Perform advanced aesthetic treatments, including laser therapy, injectables (e.g., Botox, fillers), chemical peels, and microneedling.
• Ensure the highest standards of client care, safety, and hygiene are maintained at all times.
• Educate clients on pre- and post-treatment care, product recommendations, and home skincare routines.
• Stay up-to-date with the latest advancements, techniques, and products in the medical aesthetics industry.
• Maintain accurate and confidential client records.
• Contribute to the clinic's reputation for excellence through outstanding service delivery.
• Potentially mentor or train junior members of the aesthetic team.

• Registered Nurse (RGN) or equivalent medical qualification.
• Minimum of 5 years of experience as an Aesthetic Practitioner, with a proven track record of performing a wide range of treatments.
• Expertise in facial anatomy, dermatology, and aesthetic procedures.
• Certified in administering injectables (e.g., Level 7 qualification) and proficient with various laser/light-based devices.
• Excellent communication, client management, and sales skills.
• Strong understanding of CQC regulations and medical ethics.
• A passion for beauty and aesthetics, with a keen eye for detail.
• Ability to work effectively within a team and independently.
• Professional, empathetic, and discreet demeanor.